6,353 results
Search Results
2. Mapping Treatment Advances in the Neurobiology of Binge Eating Disorder: A Concept Paper
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Brooke Donnelly and Phillipa Hay
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eating disorder ,binge eating disorder ,neurobiology ,genome ,gut microbiota ,treatment ,Nutrition. Foods and food supply ,TX341-641 - Abstract
Binge eating disorder (BED) is a complex and heritable mental health disorder, with genetic, neurobiological, neuroendocrinological, environmental and developmental factors all demonstrated to contribute to the aetiology of this illness. Although psychotherapy is the gold standard for treating BED, a significant subgroup of those treated do not recover. Neurobiological research highlights aberrances in neural regions associated with reward processing, emotion processing, self-regulation and executive function processes, which are clear therapeutic targets for future treatment frameworks. Evidence is emerging of the microbiota-gut-brain axis, which may mediate energy balance, high-lighting a possible underlying pathogenesis factor of BED, and provides a potential therapeutic strategy.
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- 2024
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3. Influence of Probiotics on the Animal Gut Microbiota and Their Impact on the Bioavailability of Toxic Agents: An Opinion Paper
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Adrián Hernández-Mendoza, Aarón F. González-Córdova, and Marcel Martínez-Porchas
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probiotics ,gut microbiota ,xenobiotic absorption ,bioremediation ,dysbiosis ,toxic agent ,Nutrition. Foods and food supply ,TX341-641 - Published
- 2022
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4. Mechanisms, therapeutic implications, and methodological challenges of gut microbiota and cardiovascular diseases: a position paper by the ESC Working Group on Coronary Pathophysiology and Microcirculation.
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Tousoulis, Dimitris, Guzik, Tomasz, Padro, Teresa, Duncker, Dirk J, Luca, Giuseppe De, Eringa, Etto, Vavlukis, Marija, Antonopoulos, Alexios S, Katsimichas, Themistoklis, Cenko, Edina, Djordjevic-Dikic, Ana, Fleming, Ingrid, Manfrini, Olivia, Trifunovic, Danijela, Antoniades, Charalambos, and Crea, Filippo
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GUT microbiome , *PATHOLOGICAL physiology , *CARDIOVASCULAR diseases , *HUMAN microbiota , *CORONARY artery disease - Abstract
The human gut microbiota is the microbial ecosystem in the small and large intestines of humans. It has been naturally preserved and evolved to play an important role in the function of the gastrointestinal tract and the physiology of its host, protecting from pathogen colonization, and participating in vitamin synthesis, the functions of the immune system, as well as glucose homeostasis and lipid metabolism, among others. Mounting evidence from animal and human studies indicates that the composition and metabolic profiles of the gut microbiota are linked to the pathogenesis of cardiovascular disease, particularly arterial hypertension, atherosclerosis, and heart failure. In this review article, we provide an overview of the function of the human gut microbiota, summarize, and critically address the evidence linking compositional and functional alterations of the gut microbiota with atherosclerosis and coronary artery disease and discuss the potential of strategies for therapeutically targeting the gut microbiota through various interventions. [ABSTRACT FROM AUTHOR]
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- 2022
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5. Mapping Treatment Advances in the Neurobiology of Binge Eating Disorder: A Concept Paper.
- Author
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Donnelly, Brooke and Hay, Phillipa
- Abstract
Binge eating disorder (BED) is a complex and heritable mental health disorder, with genetic, neurobiological, neuroendocrinological, environmental and developmental factors all demonstrated to contribute to the aetiology of this illness. Although psychotherapy is the gold standard for treating BED, a significant subgroup of those treated do not recover. Neurobiological research highlights aberrances in neural regions associated with reward processing, emotion processing, self-regulation and executive function processes, which are clear therapeutic targets for future treatment frameworks. Evidence is emerging of the microbiota-gut-brain axis, which may mediate energy balance, high-lighting a possible underlying pathogenesis factor of BED, and provides a potential therapeutic strategy. [ABSTRACT FROM AUTHOR]
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- 2024
- Full Text
- View/download PDF
6. A White Paper on Collagen Hydrolyzates and Ultrahydrolyzates: Potential Supplements to Support Joint Health in Osteoarthritis?
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Armaghan Mahmoudian, Ursule Kalvaityte, Lacey J. Favazzo, Cyro Scala de Almeida, Michael J. Zuscik, Stan Kubow, Ali Mobasheri, Christina E. Larder, Pieter J. Emans, Perola Grimberg Plapler, Michèle M. Iskandar, Paulo Cesar Hamdan, Luc J. C. van Loon, Ilona Uzieliene, Humane Biologie, RS: NUTRIM - R3 - Respiratory & Age-related Health, RS: CAPHRI - R3 - Functioning, Participating and Rehabilitation, Orthopedie, MUMC+: MA Orthopedie (9), Physiotherapy, Human Physiology and Anatomy, and Human Physiology and Sports Physiotherapy Research Group
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collagen ,medicine.medical_specialty ,Population ,Pain ,Arthritis ,Context (language use) ,Osteoarthritis ,Disease ,METABOLISM ,dietary supplements ,Denatured collagen ,Nutraceutical ,Pharmacotherapy ,Rheumatology ,FOOD ,Complementary and Alternative Medicine (S Kolasinski, Section Editor) ,Osteoarthritis/drug therapy ,Humans ,Medicine ,HYDROLYSATE ,Intensive care medicine ,education ,Nutritional supplement ,education.field_of_study ,business.industry ,Collagen hydrolyzate ,GUT MICROBIOTA ,IN-VITRO DIGESTION ,medicine.disease ,UC-II ,Clinical trial ,Collagen ultra-hydrolyzate ,ORAL TOLERANCE ,II COLLAGEN ,IMMUNE-SYSTEM ,Joint health ,Joint Diseases ,business ,DIETARY-SUPPLEMENTS - Abstract
Purpose of Review Osteoarthritis (OA) is the most common forms of arthritis in the general population, accounting for more pain and functional disability than any other musculoskeletal disease. There are currently no approved disease modifying drugs for OA. In the absence of effective pharmacotherapy, many patients with OA turn to nutritional supplements and nutraceuticals, including collagen derivatives. Collagen hydrolyzates and ultrahydrolyzates are terms used to describe collagens that have been broken down into small peptides and amino acids in the presence of collagenases and high pressure. Recent Findings This article reviews the relevant literature and serves as a White Paper on collagen hydrolyzates and ultrahydrolyzates as emerging supplements often advertised to support joint health in OA. Collagen hydrolyzates have demonstrated some evidence of efficacy in a handful of small scale clinical trials, but their ability to treat and reverse advanced joint disease remains highly speculative, as is the case for other nutritional supplements. Summary The aim of this White Paper is to stimulate research and development of collagen-based supplements for patients with OA and other musculoskeletal diseases at academic and industrial levels. This White Paper does not make any treatment recommendations for OA patients in the clinical context, but simply aims to highlight opportunities for scientific innovation and interdisciplinary collaboration, which are crucial for the development of novel products and nutritional interventions based on the best available and published evidence.
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- 2021
7. Effects of Silage Diet on Meat Quality through Shaping Gut Microbiota in Finishing Pigs
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Jiakuan Niu, Xiao Liu, Junying Xu, Fen Li, Jincan Wang, Xixi Zhang, Xu Yang, Lin Wang, Sen Ma, Defeng Li, Xiaoyan Zhu, Chengzhang Wang, Yinghua Shi, and Yalei Cui
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finishing pigs ,meat quality ,mulberry silage ,paper mulberry silage ,SCFAs ,gut microbiota ,Microbiology ,QR1-502 - Abstract
ABSTRACT With increasing demand for high-quality pork, development of green and healthy feed for finishing pigs is urgently needed. In this study, the effects and mechanisms of mulberry and paper mulberry silages on growth performance, meat quality, and intestinal health of finishing pigs were explored. Intestinal microbiota were profiled, and microbially produced short-chain fatty acids (SCFAs) were measured. The average daily gain (ADG) and feed conversion rate (FCR) with mulberry and paper mulberry silages were not significantly different from those of the control. Meat quality as measured by pork marbling and fatty acids in the longissimus dorsi was better with mulberry silage. The highest concentration of SCFAs was also with mulberry silage. According to 16S rRNA sequencing, Clostridium_sensu_stricto_1, Terrisporobacter, and Lachnospiraceae, which are important in SCFA production, were biomarkers of mulberry silage. PICRUSt functional analysis of intestinal microbes indicated that galactose metabolism, starch and sucrose metabolism, and carbohydrate digestion and absorption decreased significantly in silage treatments but increased in the control. Correlations between intestinal microbes and SCFAs and fatty acids indicated Clostridium_sensu_stricto_1, Terrisporobacter, and Lachnospiraceae were closely associated with SCFA and fatty acid contents. The results indicated that mulberry silage could increase SCFA content through shaping intestinal microbes to affect the deposition of fatty acids, which laid a solid theoretical foundation for improving pork quality. IMPORTANCE To avoid competition between people and animals for food, it is essential to develop nontraditional feeds. In this study, the effects of the silages of the unconventional feed resources mulberry and paper mulberry on meat quality of finishing pigs were examined. With mulberry silage in the diet, meat quality improved as indicated by meat color, marbling score, and beneficial fatty acids in the longissimus dorsi muscle. Pigs fed mulberry silage had the highest concentrations of short-chain fatty acids (SCFAs), and 16S rRNA sequencing identified Clostridium_sensu_stricto_1, Terrisporobacter, and Lachnospiraceae as biomarkers, which are important in SCFA production. Functions of intestinal microbes in the two silage groups primarily involved amino acid metabolism and SCFA production. Correlations between intestinal microbes and SCFAs and fatty acids indicated that Clostridium_sensu_stricto-1, Terrisporobacter, and Lachnospiraceae were closely associated with SCFA contents in the intestine and fatty acids in the longissimus dorsi.
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- 2023
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8. The interactions between traditional Chinese medicine and gut microbiota: Global research status and trends
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Shanshan Yang, Shaodong Hao, Qin Wang, Yanni Lou, Liqun Jia, and Dongmei Chen
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traditional Chinese medicine ,gut microbiota ,correlation ,research status and trends ,highly cited papers ,bibliometrics ,Microbiology ,QR1-502 - Abstract
BackgroundThere is a crosstalk between traditional Chinese medicine (TCM) and gut microbiota (GM), many articles have studied and discussed the relationship between the two. The purpose of this study is to use bibliometric analysis to explore the research status and development trends of the TCM/GM research, identify and analyze the highly cited papers relating to the TCM/GM.MethodsA literature search regarding TCM/GM publications from 2004 to 2021 was undertaken on August 13, 2022. The main information (full record and cited references) of publications was extracted from the Science Citation Index Expanded (SCI-E) of Web of Science Core Collection (WoSCC). The Bibliometrix of R package, CiteSpace and VOSviewer were used for bibliometric analysis.ResultsA total of 830 papers were included. The publication years of papers were from 2004 to 2021. The number of papers had increased rapidly since 2018. China had the most publications and made most contributions to this field. Nanjing University of Chinese Medicine and Beijing University of Chinese Medicine were in the leading productive position in TCM/GM research, Chinese Academy of Chinese Medical Sciences had the highest total citations (TC). Duan Jin-ao from Nanjing University of Chinese Medicine had the largest number of publications, and Tong Xiao-lin from China Academy of Chinese Medical Sciences had the most TC. The Journal of Ethnopharmacology had the most published papers and the most TC. The main themes in TCM/GM included the role of GM in TCM treatment of glucolipid metabolism diseases and lower gastrointestinal diseases; the mechanism of interactions between GM and TCM to treat diseases; the links between TCM/GM and metabolism; and the relationship between GM and oral bioavailability of TCM.ConclusionThis study gained insight into the research status, hotspots and trends of global TCM/GM research, identified the most cited articles in TCM/GM and analyzed their characteristics, which may inform clinical researchers and practitioners’ future directions.
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- 2022
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9. Global research trends on the links between gut microbiota and cancer immunotherapy: A bibliometric analysis (2012-2021)
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Shanshan Yang, Suya Zhao, Yixiang Ye, Liqun Jia, and Yanni Lou
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immunotherapy ,gut microbiota ,cancer ,research trends ,highly cited papers ,bibliometrics ,Immunologic diseases. Allergy ,RC581-607 - Abstract
BackgroundThere is a crosstalk between gut microbiota (GM) and cancer immunotherapy (CI). The purpose of this study is to use bibliometric analysis to identify the highly cited papers relating to GM/CI and explore the research status and development trends of the GM/CI research.MethodsA literature search regarding GM/CI publications from 2012 to 2021 was undertaken on July 4, 2022. The article titles, journals, authors, institutions, countries, total citations, keywords, and other information were extracted from the Science Citation Index Expanded (SCIE) of Web of Science Core Collection (WoSCC). The Bibliometrix of R package and VOSviewer were used for bibliometric analysis.ResultsA total of 665 papers were extracted. The number of papers has increased rapidly over the past decade, especially after 2018. The United States and China had the most publications and made great contributions to this field. Th5e Univ Texas MD Anderson Canc Ctr and Univ Paris Saclay were absolutely in the leading position in GM/CI. The most influential authors were Zitvogel L and Routy B. Frontiers in Immunology had the most publications and Science had the most total citations. Historical direct citation analysis explained the historical evolution in GM/CI. Highly cited papers and high-frequency keywords illustrated the current status and trends of GM/CI. Four clusters were identified and the important topics included the role of GM and antibiotics in CI, the methods of targeting GM to improve CI outcomes, the mechanism by which GM affects CI and the application of ICIs in melanoma. “Tumor microbiome”, “proton pump inhibitors” and “prognosis” may be the new focus of attention in the next few years.ConclusionThis study filtered global publications on GM/CI correlation and analyzed their bibliometric characteristics, identified the most cited papers in GM/CI, and gained insight into the status, hotspots and trends of global GM/CI research, which may inform researchers and practitioners of future directions.
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- 2022
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10. Mapping the relationship between atopic dermatitis and gut microbiota: a bibliometric analysis, 2014--2023.
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Yilin Wang, Bingkun Wang, Shiyou Sun, and Zhongzhi Wang
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GUT microbiome ,BIBLIOMETRICS ,ATOPIC dermatitis ,CESAREAN section ,MICROSOFT software - Abstract
Background: Atopic dermatitis (AD) is a chronic inflammatory skin condition affecting a significant portion of the population, with prevalence rates of 25% in children and 7-10% in adults. AD not only poses physical challenges but also profoundly impacts patients' mental well-being and quality of life. The stability of gut microbiota is crucial for overall health and can influence AD progression by modulating immune function, skin barrier integrity, and neuroendocrine signaling, which may be an effective target for the prevention and treatment of AD. Thus, exploring the interactions between AD and gut microbiota, particularly in infants, can provide insights into potential preventive and therapeutic strategies. This study aimed to explore the correlation between AD and gut microbiota while providing an overview of current research trends and emerging areas of interest in this field. Methods: A comprehensive search was conducted on the Web of Science Core Collection (WOSCC) for relevant publications from January 1, 2014, to December 31, 2023. English-language articles and reviews were included. Two investigators independently screened the publications, and visual analysis was performed using CiteSpace, VOSviewer, Scimago Graphica, and Microsoft Excel software. Results: A total of 804 articles were included, showing a significant increase in publications over the past decade. The United States, Wageningen University, and University Ulsan (represented by Hong SJ) had the highest number of published papers. Nutrients was the journal with the most publications, while the Journal of Allergy and Clinical Immunology had the highest number of citations and centrality among co-cited journals. Keyword visualization analysis identified "atopic dermatitis" and "gut microbiota" as central themes. Notably, there has been a notable shift in research focus over the years, with early studies concentrating on "Fecal microbiota," "caesarean section," and "first 6 months," while recent studies have highlighted the roles of "cells," "dysbiosis," and "prebiotics." This shift indicates growing interest in the underlying mechanisms and potential therapeutic interventions related to the intestinal microecology in AD treatment. Conclusion: The field of AD and gut microbiota research has evolved significantly, with an increasing focus on understanding the intricate interactions between gut microbiota and AD pathogenesis. Recent years have witnessed increased interest in understanding the relationship between AD and gut microbiota, with researchers conducting extensive studies exploring various aspects of this connection. This review analyzes research trends over the past decade, highlighting trends and hotspots in the study of AD, particularly in infants, and the role of microbiota. This review serves as a valuable reference for future investigations, aiming to provide deeper insights into this burgeoning field and suggests directions for future research. [ABSTRACT FROM AUTHOR]
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- 2024
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11. Effects of common plastic products heat exposure on cognition: Mediated by gut microbiota.
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Hu, Naifan, Pan, Degong, Yang, Yong, Pu, Lining, He, Xiaoxue, Wang, Huihui, Zhang, Xue, Du, Yurun, Yu, Zhenfan, He, Shulan, and Li, Jiangping
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GUT microbiome ,PAPER bags ,MOLECULAR biology ,COGNITIVE ability ,COGNITION ,PLASTICS - Abstract
Considering plastic exposure patterns in modern society, the effects of exposure to leachate from boiled-water treated plastic products on cognitive function was probed in mice through changes in gut microbiota diversity. In this study, Institute for Cancer Research (ICR) mice were used to establish drinking water exposure models of three popular kinds of plastic products, including non-woven tea bags, food-grade plastic bags and disposable paper cups. 16S rRNA was used to detect changes in the gut microbiota of mice. Behavioral, histopathology, biochemistry, and molecular biology experiments were used to evaluate cognitive function in mice. Our results showed that the diversity and composition of gut microbiota changed at genus level compared to control group. Nonwoven tea bags-treated mice were proved an increase in Lachnospiraceae and a decreased in Muribaculaceae in gut. Alistipes was increased under the intervention of food grade plastic bags. Muribaculaceae decreased and Clostridium increased in disposable paper cups group. The new object recognition index of mice in the non-woven tea bag and disposable paper cup groups decreased, and amyloid β-protein (Aβ) and tau phosphorylation (P-tau) protein deposition. Cell damage and neuroinflammation were observed in the three intervention groups. Totally speaking, oral exposure to leachate from boiled-water treated plastic results in cognitive decline and neuroinflammation in mammals, which is likely related to MGBA and changes in gut microbiota. [Display omitted] • Long-term plastic oral heat exposure causes gut microbiota imbalance in mice. • Long-term plastic oral heat exposure decreases cognitive function in mice. • Decline in cognitive function likely mediated by gut bacteria. • Microbial gut-brain axis and neuroinflammation play a role. [ABSTRACT FROM AUTHOR]
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- 2023
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12. Gut microbiota in early life and its influence on health and disease: A position paper by the Malaysian Working Group on Gastrointestinal Health.
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Lee, Yeong Yeh, Hassan, Siti Asma, Ismail, Intan Hakimah, Chong, Sze Yee, Raja Ali, Raja Affendi, Amin Nordin, Syafinaz, Lee, Way Seah, and Majid, Noorizan Abdul
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HUMAN microbiota ,GASTROINTESTINAL system ,GASTROINTESTINAL diseases ,PROBIOTICS ,PREBIOTICS ,HEALTH ,CONSENSUS (Social sciences) - Abstract
The role of gut microbiota in early life and its impact on gut health and subsequent diseases remain unclear. There is a lack of research and awareness in this area, especially in the Asia-Pacific region, including Malaysia. This paper reports the position of a Malaysian Working Group on some key issues surrounding gut microbiota in early life and its role in gut health and diseases, as well as experts' stand on probiotics and prebiotics. The group reached a consensus that certain factors, including elective caesarean; premature deliveries; complementary feeding; use of antibiotics, prebiotics and/or probiotics; and exposure to the external environmental, have an impact on gut microbiota in early life. However, as evidence is lacking, especially from the Asia-Pacific region, further studies are needed to understand how gut microbiota in early life affects subsequent diseases, including allergy, inflammatory bowel disease, obesity and infantile colic. Lastly, although beneficial in acute diarrhoeal disease and probably allergic eczema, probiotics (and/or prebiotics) should be used cautiously in other gut dysbiotic conditions until more data are available. [ABSTRACT FROM AUTHOR]
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- 2017
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13. Title of presented paper: The Microbiota-Gut-Brain Axis -- Role in the Pathomechanism and Pharmacotherapy of Depressive Disorders.
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Wojciechowska, Klaudia and Broszkiewicz, Michał
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DRUG therapy ,MENTAL depression ,ANTIDEPRESSANTS ,CENTRAL nervous system ,THERAPEUTICS - Abstract
Introduction and aim. Depressive disorders are a serious mental disorder, the incidence of which is constantly increasing, and thus the socio-economic cost of the disease. Research conducted since the 1960s on depression has not provided either comprehensive information on the mechanisms of the disease or provided highly effective and safe antidepressants. Recent evidence links the dysfunction of the bidirectional communication pathway between the gut microbiome and the central nervous system (known as the microbiota-gut-brain axis) to depressive disorders. Alterations in the composition and function of the intestinal microflora are observed in patients with depression. The aim of this study is to review the current knowledge on the role of the microbiota-gut-brain axis in the pathomechanism of depressive disorders and to discuss potential therapeutic implications. We will explore the use of probiotics, prebiotics, and other nutritional interventions, as well as the development of psychobiotics and other novel pharmacological agents targeting the gut microbiota, for the treatment of depressive disorders. Material and methods. Literature search: A comprehensive literature search was conducted using electronic databases such as PubMed, Embase, and Cochrane Library. The search was conducted using keywords such as "microbiota-gut-brain axis", "depressive disorders", "probiotics", "prebiotics", "psychobiotics" and "pharmacological agents targeting the gut microbiota". Study selection: Studies were included in this review if they investigated the association between the microbiota- gut-brain axis and depressive disorders. Only articles published in English and peer-reviewed were included. Data extraction: Data were extracted from the included studies, including study design, sample size, age range of participants, diagnostic criteria for depressive disorders, methods for assessing gut microbiota, and results. Analysis of literature. The results of the studies were analyzed and synthesized to provide an overview of the current knowledge on the role of the microbiota-gut-brain axis in the pathomechanism of depressive disorders. Results. The findings of the studies were discussed in the context of potential therapeutic implications. The use of probiotics, prebiotics, and other nutritional interventions, as well as the development of psychobiotics and other novel pharmacological agents targeting the gut microbiota, were explored for the treatment of depressive disorders Conclusion. The war negatively changed lifestyle of Ukrainian student via forced relocation and disability to continue education in universities. Among students were detected severe and extremely severe depression, low level of QL due to changes in mental health during war in Ukraine. [ABSTRACT FROM AUTHOR]
- Published
- 2023
14. Fortification of tempeh with encapsulated iron improves iron status and gut microbiota composition in iron deficiency anemia condition
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Jati Kusuma, Rio and Ermamilia, Aviria
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- 2018
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15. Bibliometric analysis of global research trends between gut microbiota and breast cancer: from 2013 to 2023.
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Xianguang Deng, Hua Yang, Lingjia Tian, Jie Ling, Hui Ruan, Anqi Ge, Lifang Liu, and Hongqiao Fan
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GUT microbiome ,BIBLIOMETRICS ,BREAST cancer ,CHINA-United States relations ,TUMOR microenvironment - Abstract
Background: Breast cancer is the most prevalent cancer globally and is associated with significant mortality. Recent research has provided crucial insights into the role of gut microbiota in the onset and progression of breast cancer, confirming its impact on the disease's management. Despite numerous studies exploring this relationship, there is a lack of comprehensive bibliometric analyses to outline the field's current state and emerging trends. This study aims to fill that gap by analyzing key research directions and identifying emerging hotspots. Method: Publications from 2013 to 2023 were retrieved from the Web of Science Core Collection database. The VOSviewer, R language and SCImago Graphica software were utilized to analyze and visualize the volume of publications, countries/regions, institutions, authors, and keywords in this field. Results: A total of 515 publications were included in this study. The journal Cancers was identified as the most prolific, contributing 21 papers. The United States and China were the leading contributors to this field. The University of Alabama at Birmingham was the most productive institution. Peter Bai published the most papers, while James J. Goedert was the most cited author. Analysis of highly cited literature and keyword clustering confirmed a close relationship between gut microbiota and breast cancer. Keywords such as "metabolomics" and "probiotics" have been prominently highlighted in the keyword analysis, indicating future research hotspots in exploring the interaction between metabolites in the breast cancer microenvironment and gut microbiota. Additionally, these keywords suggest significant interest in the therapeutic potential of probiotics for breast cancer treatment. Conclusion: Research on the relationship between gut microbiota and breast cancer is expanding. Attention should be focused on understanding the mechanisms of their interaction, particularly the metabolite-microbiota-breast cancer crosstalk. These insights have the potential to advance prevention, diagnosis, and treatment strategies for breast cancer. This bibliometric study provides a comprehensive assessment of the current state and future trends of research in this field, offering valuable perspectives for future studies on gut microbiota and breast cancer. [ABSTRACT FROM AUTHOR]
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- 2024
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16. The Replacement of Fish Meal with Poultry By-Product Meal and Insect Exuviae: Effects on Growth Performance, Gut Health and Microbiota of the European Seabass, Dicentrarchus labrax.
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Rimoldi, Simona, Di Rosa, Ambra Rita, Armone, Rosangela, Chiofalo, Biagina, Hasan, Imam, Saroglia, Marco, Kalemi, Violeta, and Terova, Genciana
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SHORT-chain fatty acids ,SUSTAINABILITY ,SUSTAINABLE aquaculture ,FISH productivity ,FISH meal ,EUROPEAN seabass - Abstract
This study addressed the urgent need for sustainable protein sources in aquaculture due to the depletion of marine resources and rising costs. Animal protein sources, particularly poultry by-product meal (PBM) and insect exuviae meal, were investigated as viable alternatives to fishmeal (FM). The research study confirmed the successful replacement of FM with a combination of PBM and insect exuviae meal (up to 50%) in the diet of European seabass without compromising growth, feed conversion, gut health, and liver fat content. In particular, growth was robust with both PBM formulations, with the 25% PBM diet showing better results. Histological examinations showed good gut and liver health, contradicting the concerns of previous studies. This paper emphasizes the importance of holistic analyzes that go beyond growth parameters and include histomorphological investigations. The results show that PBM in combination with insect/exuviae meal is well tolerated by seabass, which is consistent with reports in the literature of it mitigating negative effects on gut health. A detailed analysis of the microbiota revealed a decrease in the Firmicutes/Proteobacteria ratio due to an increase in potentially pathogenic bacteria. However, the formulation containing insect exuviae partially counteracted this effect by preserving the beneficial Lactobacillus and promoting the synthesis of short-chain fatty acids (SCFAs), particularly butyrate. Chitin-rich components from insect exuviae were associated with improved gut health, which was supported by the increased production of SCFAs, which are known for their anti-inflammatory properties. This paper concludes that a combination of PBM and insect/exuviae meal can replace up to 50% of FM in the diet of seabass, supporting sustainable aquaculture practices. Despite some changes in the microbiota, the negative effects are mitigated by the addition of insect exuviae, highlighting their potential as a prebiotic to increase fish productivity and contribute to a circular economy in aquaculture. [ABSTRACT FROM AUTHOR]
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- 2024
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17. Relationship between gut microbiota and the pathogenesis of gestational diabetes mellitus: a systematic review.
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Sheng Ma, Yuping Wang, Xiaoxia Ji, Sunjuan Dong, Shengnan Wang, Shuo Zhang, Feiying Deng, Jingxian Chen, Benwei Lin, Khan, Barkat Ali, Weiting Liu, and Kaijian Hou
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GESTATIONAL diabetes ,GUT microbiome ,PANCREATIC beta cells ,SHORT-chain fatty acids ,INSULIN sensitivity ,LITERATURE reviews - Abstract
Introduction: Gestational diabetes mellitus (GDM) is a form of gestational diabetes mellitus characterized by insulin resistance and abnormal function of pancreatic beta cells. In recent years, genomic association studies have revealed risk and susceptibility genes associated with genetic susceptibility to GDM. However, genetic predisposition cannot explain the rising global incidence of GDM, which may be related to the increased influence of environmental factors, especially the gut microbiome. Studies have shown that gut microbiota is closely related to the occurrence and development of GDM. This paper reviews the relationship between gut microbiota and the pathological mechanism of GDM, in order to better understand the role of gut microbiota in GDM, and to provide a theoretical basis for clinical application of gut microbiota in the treatment of related diseases. Methods: The current research results on the interaction between GDM and gut microbiota were collected and analyzed through literature review. Keywords such as "GDM", "gut microbiota" and "insulin resistance" were used for literature search, and the methodology, findings and potential impact on the pathophysiology of GDM were systematically evaluated. Results: It was found that the composition and diversity of gut microbiota were significantly associated with the occurrence and development of GDM. Specifically, the abundance of certain gut bacteria is associated with an increased risk of GDM, while other changes in the microbiome may be associated with improved insulin sensitivity. In addition, alterations in the gut microbiota may affect blood glucose control through a variety of mechanisms, including the production of short-chain fatty acids, activation of inflammatory pathways, and metabolism of the B vitamin group. Discussion: The results of this paper highlight the importance of gut microbiota in the pathogenesis of GDM. The regulation of the gut microbiota may provide new directions for the treatment of GDM, including improving insulin sensitivity and blood sugar control through the use of probiotics and prebiotics. However, more research is needed to confirm the generality and exact mechanisms of these findings and to explore potential clinical applications of the gut microbiota in the management of gestational diabetes. In addition, future studies should consider the interaction between environmental and genetic factors and how together they affect the risk of GDM. [ABSTRACT FROM AUTHOR]
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- 2024
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18. The role of gut microbiota in the development of salt-sensitive hypertension and the possible preventive effect of exercise.
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Chrysant, Steven G.
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GUT microbiome ,SHORT-chain fatty acids ,HYPERTENSION ,HUMAN-animal relationships - Abstract
The aim of the present study is to analyze the data indicating an association between high salt intake and the gastrointestinal microbiota in the development of salt-sensitive hypertension in animals and men. It is also, to discuss the preventive effects of exercise on gut-induced hypertension by favorably modifying the composition of gut microbiota. Salt sensitivity is quite common, accounting for 30%–60% in hypertensive subjects. Recently, a novel cause for salt-sensitive hypertension has been discovered through the action of gut microbiota by the secretion of several hormones and the action of short chain fatty acids (SCFAs). In addition, recent studies indicate that exercise might favorably modify the adverse effects of gut microbiota regarding their effects on BP. To identify the role of gut microbiota on the incidence of hypertension and CVD and the beneficial effect of exercise, a Medline search of the English literature was conducted between 2018 and 2023 and 42 pertinent papers were selected. The analysis of data from the selected papers disclosed that the gut microbiota contribute significantly to the development of salt-sensitive hypertension and that exercise modifies their gut composition and ameliorates their adverse effects on BP. [ABSTRACT FROM AUTHOR]
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- 2024
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19. The role of the gut microbiota in the pathogenesis and treatment of Alzheimer disease - review.
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Wojtuś, Magda, Tomaszuk, Sebastian, and Wąsik, Karolina
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ENTEROTYPES ,GUT microbiome ,ALZHEIMER'S disease ,THERAPEUTICS ,FECAL microbiota transplantation ,WESTERN diet ,PATHOGENESIS - Abstract
Introduction and purpose: Currently, the role of the gut microbiota in the pathogenesis of different diseases is being widely researched, the understanding of whether the dysbiosis of the gut flora demonstrates the significant role in Alzheimer disease (AD) is accentuated. The aim of this paper is to summarize the existing paper about the role of the gut microbiota - its diversity, stability and composition in this condition. The search was conducted using PubMed and Google Scholarship databases. Brief description of the state of knowledge: It is still uncertain if alteration in gut microbiome is a consequence of AD or its risk factor, but some findings suggest that the intestinal flora is able to influence the activity of the brain and lead to its dysfunctions. There is also the association between composition of the gut microbiome and AD. Results indicate that affected patients had less heterogeneity in their microbiome and the progression of AD led to alterations in the bacterial flora. Introducing modifications of the gut microbiota is considered as a therapeutic option for AD. Following personalized diet, probiotics, prebiotics and synbiotics administration or fecal microbiota transplantation (FMT) may be beneficial for affected patients. Conclusions: The subject of the role of the gut microbiota merits further research as foregoing results of conducted studies are pointing to its possibly meaningful role. Presently, still more data is needed as most of the research was collected on animal models and the analysis conducted on humans remains insufficient. We conclude that further studies are warranted in order to fully understand the pathophysiology of the disease and the possible usefulness of microbiome therapy. [ABSTRACT FROM AUTHOR]
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- 2024
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20. Gut microbiota and immunity in health and diseases: a review
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Okolie, Michael Chukwuma, Edo, Great Iruoghene, Ainyanbhor, Irene Ebosereme, Jikah, Agatha Ngukuran, Akpoghelie, Patrick Othuke, Yousif, Emad, Zainulabdeen, Khalid, Isoje, Endurance Fegor, Igbuku, Ufuoma Augustina, Orogu, Joshua Othuke, Owheruo, Joseph Oghenewogaga, Essaghah, Arthur Efeoghene Athan, and Umar, Huzaifa
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- 2024
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21. The gut microbiota of non-obese Japanese pregnant women with gestational diabetes mellitus
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Fang He, Kenji Miyazawa, Gaku Harata, Shinji Tanigaki, Yoichi Kobayashi, and Kei Tanaka
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endocrine system diseases ,Immunology ,non-obesity ,Physiology ,Gut flora ,Applied Microbiology and Biotechnology ,Microbiology ,Non obese ,medicine ,Collinsella ,Full Paper ,gut microbiota ,biology ,business.industry ,Gastroenterology ,nutritional and metabolic diseases ,Akkermansia ,medicine.disease ,biology.organism_classification ,female genital diseases and pregnancy complications ,gestational diabetes mellitus ,Gestational diabetes ,business ,Food Science - Abstract
Recent evidence has shown that gut microbiota dysbiosis is associated with development of gestational diabetes mellitus (GDM). However, the gut microbiota composition of non-obese women with GDM, which accounts for a relatively large percentage of Asian GDM, is unknown. We investigated the characteristics of gut microbiota of Japanese pregnant women with GDM. Fecal samples from Japanese pregnant women with GDM (n=20) and normal glucose tolerance (NGT, n=16) were collected at the time of GDM diagnosis (T1), at 35–37 weeks of gestation (T2), and at 4 weeks postpartum (T3). Gut microbiota composition was characterized from fecal DNA by sequencing of 16S rRNA genes. Serum samples were collected late in the third trimester, and the circulating levels of adiponectin and IL-6 were measured by ELISA. At the genus level, Peptostreptococcaceae Romboutsia was enriched in GDM women at T1 (p=0.008) and T2 (p=0.047). The women with lower serum adiponectin tended to have more Romboutsia. The Shannon index was significantly lower in the GDM women at T3 than in the NGT women (p=0.008), and that of the GDM women decreased significantly from T2 to T3 (p=0.02). No significant difference in bacterial community structure was found in a beta diversity analysis. The non-obese GDM women (body mass index
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- 2022
22. Research reviews and prospects of gut microbiota in liver cirrhosis: a bibliometric analysis (2001-2023).
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Xiaofei Zhu, Ziyuan Zhou, and Xiaxia Pan
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GUT microbiome ,CIRRHOSIS of the liver ,BIBLIOMETRICS ,FECAL microbiota transplantation ,LITERATURE reviews - Abstract
Introduction: The gut-liver axis has emerged as a focal point in chronic liver disorders, prompting more research into the role of the gut microbiota in liver cirrhosis. In individuals with liver cirrhosis, changes in the structure and function of the gut microbiota are closely tied to clinical prognosis. However, there is a scarcity of bibliometric evaluations conducted in this particular field. Methods: This study is aiming to conduct a complete analysis of the knowledge structure and centers pertaining to gut microbiota in liver cirrhosis using bibliometric methods. Publications on gut microbiota and liver cirrhosis from 2001 to 2023 are sourced from the Web of Science Core Collection. For the bibliometric analysis, we employ VOSviewer, CiteSpace, and the R package "bibliometrix". Results: Our study encompasses a comprehensive collection of 3109 articles originating from 96 countries, with notable contributions from leading nations such as the United States and China. The quantity of publications concerning the gut microbiota of liver cirrhosis rises annually. The University of California San Diego, Virginia Commonwealth University, Zhejiang University are the primary research institutions. World Journal of Gastroenterology publishes the most papers in this field, while hepatology is the most frequently co-cited journal. These publications come from a total of 15,965 authors, and the most prolific authors are Bajaj Jasmohan S., Schnabl Bernd and Gillevet Patrick M., while the most co-cited authors are Bajaj Jasmohan S., Younossi Zobair M., and Reiner Wiest. In addition, "dysbiosis", "gut microbiota", "intestinal barrier", "fecal microbiota transplantation", and "complementsystem" are the primary keywords of research trends in recent years. Discussion: This study offering a comprehensive insight into the research dynamics surrounding gut microbiota in patients with liver cirrhosis. It delineates the current research frontiers and hotspots, serving as a valuable guide for scholars. [ABSTRACT FROM AUTHOR]
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- 2024
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23. Gastrodin attenuates perfluorooctanoic acid-induced liver injury by regulating gut microbiota composition in mice
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Shumin Ma, Yanyan Sun, Xueting Zheng, and Yang Yang
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Male ,short-chain fatty acids ,Bioengineering ,Protective Agents ,Applied Microbiology and Biotechnology ,gastrodin ,perfluorooctanoic acid ,Glucosides ,Animals ,Cecum ,Benzyl Alcohols ,Phylogeny ,Fluorocarbons ,gut microbiota ,General Medicine ,Fatty Acids, Volatile ,Gastrointestinal Microbiome ,Mice, Inbred C57BL ,Disease Models, Animal ,Oxidative Stress ,Liver ,Cytokines ,Caprylates ,Inflammation Mediators ,TP248.13-248.65 ,Research Article ,Research Paper ,Hepatomegaly ,liver injury ,Biotechnology - Abstract
Perfluorooctanoic acid (PFOA) can accumulate in the livers of humans and animals via the food chain, resulting into liver injury, which is closely related to intestinal flora dysbiosis. Gastrodin has been reported to have hepatoprotective effect. However, whether gastrodin can alleviate PFOA-induced liver injury via modulating gut microbiota remains unclear. Herein, a PFOA-induced liver injury model was established by gavage of PFOA (5 mg/kg body weight) in 2% Tween 80 solution once daily for 6 weeks in mice, and then gastrodin in saline (20 mg/kg body weight) was used once daily for 8 weeks to treat liver damage. The biochemical indexes associated with liver function, oxidative stress, and inflammatory factors were examined. Hematoxylin-eosin staining was used to determine the liver histopathological changes. Besides, 16S rRNA sequencing was used to analyze the difference of gut microbiota between the model and treatment groups. The results showed that gastrodin significantly improved the oxidative stress caused by PFOA. Intestinal flora analysis showed that gastrodin treatment significantly increased the relative abundance of probiotics, such as Lactobacillus, Bifidobacterium, and Bacteroides, while the harmful bacteria, including Desulfovibrio were decreased. Gastrodin treatment also significantly increased the level of short-chain fatty acids (SCFAs), such as butyric acid and isobutyric acid. Spearman correlation analysis showed that the composition changes of gut microbiota and SCFAs increase were both beneficial to alleviate the liver injury caused by PFOA. To sum up, gastrodin can effectively alleviate PFOA-induced liver injury through regulating gut microbiota composition.
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- 2021
24. Alteration of the gut microbiota following SARS-CoV-2 infection correlates with disease severity in hamsters
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Valentin Sencio, Arnaud Machelart, Cyril Robil, Nicolas Benech, Eik Hoffmann, Chloé Galbert, Lucie Deryuter, Séverine Heumel, Aline Hantute-Ghesquier, Anne Flourens, Priscille Brodin, Fabrice Infanti, Virgile Richard, Jean Dubuisson, Corinne Grangette, Thierry Sulpice, Isabelle Wolowczuk, Florence Pinet, Vincent Prévot, Sandrine Belouzard, François Briand, Martine Duterque-Coquillaud, Harry Sokol, François Trottein, CHU Lille, Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 (CIIL), Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)-Centre National de la Recherche Scientifique (CNRS), Centre de Recherche Saint-Antoine (CRSA), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), CHU Saint-Antoine [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Cancer Heterogeneity, Plasticity and Resistance to Therapies - UMR 9020 - U 1277 (CANTHER), Réseau International des Instituts Pasteur (RIIP), Sciempath Labo [Larçay] (SL), Physiogenex, Facteurs de Risque et Déterminants Moléculaires des Maladies liées au Vieillissement - U 1167 (RID-AGE), Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Lille Neurosciences & Cognition - U 1172 (LilNCog), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Excellence Laboratory LabEx DISTALZ, MICrobiologie de l'ALImentation au Service de la Santé (MICALIS), AgroParisTech-Université Paris-Saclay-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Centre National de la Recherche Scientifique (CNRS)-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)-Université de Lille-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon, Centre de Recherche Saint-Antoine (CR Saint-Antoine), Sorbonne Université (SU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Saint-Antoine [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Mécanismes de tumorigenèse et thérapies ciblées, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Lille Neurosciences & Cognition - U 1172 (LilNCog (ex-JPARC)), Gestionnaire, HAL Sorbonne Université 5, Wolowczuk, Isabelle, and ANR-17-CE15-0020,ACROBAT,Rôle de l'axe poumon/intestin/moelle osseuse et du microbiote au cours de la grippe(2017)
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Microbiology (medical) ,Male ,[SDV]Life Sciences [q-bio] ,RC799-869 ,Microbiology ,digestive system ,Severity of Illness Index ,03 medical and health sciences ,0302 clinical medicine ,[SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases ,markers of disease severity ,Cricetinae ,Animals ,Humans ,030304 developmental biology ,[SDV.MP.VIR] Life Sciences [q-bio]/Microbiology and Parasitology/Virology ,0303 health sciences ,Bacteria ,Mesocricetus ,gut microbiota ,Gastroenterology ,hamsters ,Diseases of the digestive system. Gastroenterology ,Fatty Acids, Volatile ,3. Good health ,Gastrointestinal Microbiome ,COVID-19 Drug Treatment ,[SDV] Life Sciences [q-bio] ,Disease Models, Animal ,sars-cov-2 ,Infectious Diseases ,covid-19 ,[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology ,[SDV.MHEP.MI] Life Sciences [q-bio]/Human health and pathology/Infectious diseases ,030211 gastroenterology & hepatology ,Research Article ,Research Paper - Abstract
Mounting evidence suggests that the gut-to-lung axis is critical during respiratory viral infections. We herein hypothesized that disruption of gut homeostasis during severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection may associate with early disease outcomes. To address this question, we took advantage of the Syrian hamster model. Our data confirmed that this model recapitulates some hallmark features of the human disease in the lungs. We further showed that SARS-CoV-2 infection associated with mild intestinal inflammation, relative alteration in intestinal barrier property and liver inflammation and altered lipid metabolism. These changes occurred concomitantly with an alteration of the gut microbiota composition over the course of infection, notably characterized by a higher relative abundance of deleterious bacterial taxa such as Enterobacteriaceae and Desulfovibrionaceae. Conversely, several members of the Ruminococcaceae and Lachnospiraceae families, including bacteria known to produce the fermentative products short-chain fatty acids (SCFAs), had a reduced relative proportion compared to non-infected controls. Accordingly, infection led to a transient decrease in systemic SCFA amounts. SCFA supplementation during infection had no effect on clinical and inflammatory parameters. Lastly, a strong correlation between some gut microbiota taxa and clinical and inflammation indices of SARS-CoV-2 infection severity was evidenced. Collectively, alteration of the gut microbiota correlates with disease severity in hamsters making this experimental model valuable for the design of interventional, gut microbiota-targeted, approaches for the control of COVID-19. Abbreviations: SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; COVID-19, coronavirus disease 2019; SCFAs, short-chain fatty acids; dpi, day post-infection; RT-PCR, reverse transcription polymerase chain reaction; IL, interleukin. ACE2, angiotensin converting enzyme 2; TMPRSS2, transmembrane serine protease 2.
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- 2022
25. Bacteroides acidifaciens in the gut plays a protective role against CD95-mediated liver injury
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Hesuiyuan Wang, Qing Wang, Chengmao Yang, Mingming Guo, Xiaoyue Cui, Zhe Jing, Yujie Liu, Wanjin Qiao, Hang Qi, Hongyang Zhang, Xu Zhang, Na Zhao, Mengjuan Zhang, Min Chen, Song Zhang, Haijin Xu, Liqing Zhao, Mingqiang Qiao, and Zhenzhou Wu
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Microbiology (medical) ,Infectious Diseases ,gut microbiota ,intestinal flora dysbiosis ,cd95 ,gsh ,Gastroenterology ,hepatitis ,RC799-869 ,Diseases of the digestive system. Gastroenterology ,Microbiology ,Research Article ,Research Paper - Abstract
The intestinal flora plays an important role in the development of many human and animal diseases. Microbiome association studies revealed the potential regulatory function of intestinal bacteria in many liver diseases, such as autoimmune hepatitis, viral hepatitis and alcoholic hepatitis. However, the key intestinal bacterial strains that affect pathological liver injury and the underlying functional mechanisms remain unclear. We found that the gut microbiota from gentamycin (Gen)-treated mice significantly alleviated concanavalin A (ConA)-induced liver injury compared to vancomycin (Van)-treated mice by inhibiting CD95 expression on the surface of hepatocytes and reducing CD95/CD95L-mediated hepatocyte apoptosis. Through the combination of microbiota sequencing and correlation analysis, we isolated 5 strains with the highest relative abundance, Bacteroides acidifaciens (BA), Parabacteroides distasonis (PD), Bacteroides thetaiotaomicron (BT), Bacteroides dorei (BD) and Bacteroides uniformis (BU), from the feces of Gen-treated mice. Only BA played a protective role against ConA-induced liver injury. Further studies demonstrated that BA-reconstituted mice had reduced CD95/CD95L signaling, which was required for the decrease in the L-glutathione/glutathione (GSSG/GSH) ratio observed in the liver. BA-reconstituted mice were also more resistant to alcoholic liver injury. Our work showed that a specific murine intestinal bacterial strain, BA, ameliorated liver injury by reducing hepatocyte apoptosis in a CD95-dependent manner. Determination of the function of BA may provide an opportunity for its future use as a treatment for liver disease.
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- 2022
26. Gut-brain axis and neurodegeneration: mechanisms and therapeutic potentials.
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Park, Kelly Jimin and Gao, Yao
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FECAL microbiota transplantation ,GUT microbiome ,SHORT-chain fatty acids ,MICROBIAL ecology ,FATTY acid derivatives - Abstract
This paper reviews the effects of gut microbiota in regulating neurodegenerative diseases through controlling gut-brain axis. Specific microbial populations and their metabolites (short-chain fatty acids and tryptophan derivatives) regulate neuroinflammation, neurogenesis and neural barrier integrity. We then discuss ways by which these insights lead to possible interventions - probiotics, prebiotics, dietary modification, and fecal microbiota transplantation (FMT). We also describe what epidemiological and clinical studies have related certain microbiota profiles with the courses of neurodegenerative diseases and how these impact the establishment of microbiome-based diagnostics and individualized treatment options. We aim to guide microbial ecology research on this key link to neurodegenerative disorders and also to highlight collaborative approaches to manage neurological health by targeting microbiome-related factors. [ABSTRACT FROM AUTHOR]
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- 2024
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27. Revisiting the potential anti-obesity effects of kimchi and lactic acid bacteria isolated from kimchi: a lustrum of evidence.
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Sharma, Anshul and Lee, Hae-Jeung
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LACTIC acid bacteria ,HOLISTIC medicine ,LITERATURE reviews ,PEPPERS ,BRASSICACEAE ,ENTEROTYPES - Abstract
Kimchi, a renowned and culturally significant Korean dish, has gained global recognition as a superfood due to its abundant nutritional content and positive impact on human health. The process of producing kimchi involves the fermentation of various vegetables using lactic acid bacteria (LAB). The primary genera of kimchi LAB encompass Lactobacillus, Lactococcus, Leuconostoc, Pediococcus, and Weissella. Impressively, kimchi comes in over 200 varieties with cruciferous vegetables as its main ingredients, complemented by a range of secondary ingredients that contribute to its nutritional and holistic health benefits. These secondary ingredients include salted fish, ginger, garlic, and red pepper powder. Due to its various functional properties, kimchi has attracted considerable interest. Kimchi has been extensively studied, and its recognized health benefits, including anti-oxidant, anti-tumor, anti-inflammatory, anti-microbial, anti-obesity, hepatoprotective, neuroprotection, anti-allergic, regulation of immunological responses, and many more, have been covered in many review papers. A current literature review regarding the anti-obesity properties of kimchi and kimchi LAB is currently lacking. Therefore, the present review has directed its attention towards the literature concerning the anti-obesity properties of kimchi and LAB derived from kimchi over the last five years. [ABSTRACT FROM AUTHOR]
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- 2024
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28. Gut–Brain Axis and Psychopathology: Exploring the Impact of Diet with a Focus on the Low-FODMAP Approach.
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Ribichini, Emanuela, Scalese, Giulia, Mocci, Chiara, and Severi, Carola
- Abstract
Background: The gut–brain axis (GBA) is a bidirectional communication network connecting the central nervous system with the gastrointestinal (GI) tract, influencing both mental and physical health. Recent research has underscored the significant role of diet in modulating this axis, with attention to how specific dietary patterns can impact anxiety and depression, particularly when linked to disorders of gut–brain interaction (DGBIs), like intestinal bowel syndrome (IBS). Aims and Methods: This narrative review examines the effects of specific diet regimens on the GBA and its potential role in managing psychopathology, focusing on anxiety and depression, IBS, and the low-FODMAP diet. We conducted a search on PubMed and MEDLINE by combining the following key terms: "Gut–Brain Axis", "Irritable Bowel Syndrome", "Low FODMAP diet", "Mediterranean Diet", "Psychopathology", "Anxiety and Depression", and "Gut Microbiota". We applied the following filters: "Clinical Trials", "Randomized Controlled Trials", "Reviews", "Meta-Analyses", and "Systematic Reviews". In total, 59 papers were included. Results: Low-FODMAP diet, originally developed to alleviate GI symptoms in IBS, may also positively influence mental health by modulating the GBA and improving the gut microbiota (GM) composition. New insights suggest that combining the low-FODMAP diet with the Mediterranean diet could offer a synergistic effect, enhancing both GI and psychological therapeutic outcomes. Conclusions: Understanding the complex interactions between diet, the GM, and mental health opens new avenues for holistic approaches to managing psychopathology, particularly when linked to GI symptoms. [ABSTRACT FROM AUTHOR]
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- 2024
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29. 益生菌缓解高尿酸血症:研究现状、 作用机制及面临的挑战.
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杨新如, 唐甲越, 曾小群, 吴 振, 杜启伟, and 涂茂林
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XANTHINE oxidase ,GUT microbiome ,URIC acid ,METABOLIC disorders ,HYPERURICEMIA - Abstract
Copyright of Science & Technology of Food Industry is the property of Science & Technology of Food Industry Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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- 2024
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30. Tryptophan Metabolism Disorder-Triggered Diseases, Mechanisms, and Therapeutic Strategies: A Scientometric Review.
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Chen, Xue, Xu, Dong, Yu, Jie, Song, Xu-Jiao, Li, Xue, and Cui, Yuan-Lu
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Background: Tryptophan is widely present in foods such as peanuts, milk, and bananas, playing a crucial role in maintaining metabolic homeostasis in health and disease. Tryptophan metabolism is involved in the development and progression of immune, nervous, and digestive system diseases. Although some excellent reviews on tryptophan metabolism exist, there has been no systematic scientometric study as of yet. Methods: This review provides and summarizes research hotspots and potential future directions by analyzing annual publications, topics, keywords, and highly cited papers sourced from Web of Science spanning 1964 to 2022. Results: This review provides a scientometric overview of tryptophan metabolism disorder-triggered diseases, mechanisms, and therapeutic strategies. Conclusions: The gut microbiota regulates gut permeability, inflammation, and host immunity by directly converting tryptophan to indole and its derivatives. Gut microbial metabolites regulate tryptophan metabolism by activating specific receptors or enzymes. Additionally, the kynurenine (KYN) pathway, activated by indoleamine-2, 3-dioxygenase (IDO) and tryptophan 2, 3-dioxygenase, affects the migration and invasion of glioma cells and the development of COVID-19 and depression. The research and development of IDO inhibitors help to improve the effectiveness of immunotherapy. Tryptophan metabolites as potential markers are used for disease therapy, guiding clinical decision-making. Tryptophan metabolites serve as targets to provide a new promising strategy for neuroprotective/neurotoxic imbalance affecting brain structure and function. In summary, this review provides valuable guidance for the basic research and clinical application of tryptophan metabolism. [ABSTRACT FROM AUTHOR]
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- 2024
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31. Mitogenomic profiling and gut microbial analysis of the newly identified polystyrene-consuming lesser mealworm in Kenya.
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Ndotono, Evalyne W., Tanga, Chrysantus M., Kelemu, Segenet, and Khamis, Fathiya M.
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MITOCHONDRIAL DNA ,PLASTIC scrap ,CIRCULAR economy ,BIODEGRADABLE plastics ,GUT microbiome ,OVERALL survival - Abstract
Plastic waste has recently become a major global environmental concern and one of the biggest challenges has been seeking for alternative management options. Several studies have revealed the potential of several coleopteran species to degrade plastics, and this is the first research paper on plastic-degradation potential by lesser mealworms from Africa. This study evaluated the whole mitogenomic profile of the lesser mealworm to further identify the insect. The ability of the mealworm to consume Polystyrene (PS) was also evaluated alongside its associated gut microbiota diversity. Our results showed a complete circular mitochondrial genome which clustered closely to the Alphitobius genus but also suggested that our insect might be a new subspecies which require further identification. During the PS feeding trials, overall survival rates of the larvae decreased when fed a sole PS diet while PS intake was observed to increase over a 30-day period. The predominant bacteria observed in larvae fed PS diets were Kluyvera, Lactococcus, Klebsiella, Enterobacter, and Enterococcus, while Stenotrophomonas dominated the control diet. These findings demonstrated that the newly identified lesser mealworm can survive on a PS diet and has a consortium of important bacteria strongly associated with PS degradation. This work provides a better understanding of bioremediation applications, paving the way for further research into the metabolic pathways of plastic-degrading microbes and bringing hope to solving plastic waste pollution while providing high-value insect protein towards a circular economy. [ABSTRACT FROM AUTHOR]
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- 2024
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32. The impact of gut microbiota on morbidities in preterm infants.
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Lai, Mei‐Yin, Chang, Yin‐Hsi, Lee, Chien‐Chung, Chiu, Cheng‐Hsun, Chiang, Ming‐Chou, Wu, Wei‐Chi, Yeh, Yuan‐Ming, Wu, Wei‐Hung, Wu, Po‐Yi, and Ho, Ming‐Chih
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PREMATURE infants ,GUT microbiome ,BRONCHOPULMONARY dysplasia ,DYSBIOSIS ,INFANT health ,ENTEROCOLITIS - Abstract
The gut microbiota undergoes substantial development from birth, and its development in the initial years of life has a potentially lifelong effect on the health of the individual. However, various factors can disrupt the development of the gut microbiota, leading to a condition known as dysbiosis, particularly in preterm infants. Current studies involving adults have suggested that the gut microbiota not only influences the gut but also has multidimensional effects on remote organs; these pathways are often referred to as the gut–organ axis. Imbalance of the gut microbiota may lead to the development of multiple diseases. Recent studies have revealed that gut dysbiosis in preterm infants may cause several acute morbidities—such as necrotizing enterocolitis, late‐onset sepsis, bronchopulmonary dysplasia, and retinopathy of prematurity—and it may also influence long‐term outcomes including neurodevelopment and somatic growth. This review mainly presents the existing evidence regarding the relationships between the gut microbiota and these morbidities in preterm infants and explores the role of the gut–organ axis in these morbidities. This paper thus offers insights into the future perspectives on microbiota interventions for promoting the health of preterm infants. [ABSTRACT FROM AUTHOR]
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- 2024
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33. Analysis of gut microbiota and metabolites in patients with rheumatoid arthritis and identification of potential biomarkers
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Donge Tang, Jingquan He, Lixiong Liu, Chiyu Ma, Yumei Chen, Dongzhou Liu, Weier Dai, Xiaoping Hong, Fengping Zheng, Yong Dai, and Chengxin Zhu
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rheumatoid arthritis ,Adult ,DNA, Bacterial ,Aging ,Gut flora ,medicine.disease_cause ,Arthritis, Rheumatoid ,Lactobacillus ,RNA, Ribosomal, 16S ,medicine ,Humans ,Microbiome ,metabolites ,biology ,gut microbiota ,Streptococcus ,Fatty Acids ,Verrucomicrobia ,Bacteroidetes ,biomarkers ,Akkermansia ,Cell Biology ,Middle Aged ,biology.organism_classification ,Gastrointestinal Microbiome ,Immunology ,Fatty Acids, Unsaturated ,Metabolome ,Bacteroides ,Research Paper - Abstract
Rheumatoid arthritis (RA) is an autoimmune disease described by joint destruction, synovitis and pannus formation. The gut microbiota acts as an environmental factor that plays an important role in RA, but little research regarding the etiopathogenic mechanisms of the microbiome in RA has been carried out. We used an integrated approach of 16S rRNA gene sequencing and ultrahigh-performance liquid chromatography-mass spectrometry-based metabolomics to analyze the structure and diversity of the intestinal flora and metabolites of the gut microbiota in RA patients compared with healthy subjects. In this study, α-diversity analysis of the gut microbiota showed that there was no significant difference between the healthy control (HC) and RA groups. However, β-diversity analysis showed that there was a significant difference between the two groups. Further analysis of alteration of the gut microbiota revealed that at the phylum level, the relative abundance of p_Bacteroidetes was significantly decreased in the RA group, while that of Verrucomicrobia and Proteobacteria was significantly increased in the RA group. At the genus level, Bacteroides, Faecalibacterium and some probiotics were decreased in the RA group, while 97 genera, including Lactobacillus, Streptococcus and Akkermansia, were increased in the RA group. Seventy-four differentially abundant metabolites were identified between the HC and RA groups, and we identified two potential biomarkers (9,12-octadecadiynoic acid and 10Z-nonadecenoic acid) in RA.
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- 2021
34. Suppressed inflammation in obese children induced by a high-fiber diet is associated with the attenuation of gut microbial virulence factor genes
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Menghui Zhang, Liping Zhao, Hui Li, and Guojun Wu
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Dietary Fiber ,Microbiology (medical) ,Pediatric Obesity ,obesity ,prader-willi syndrome ,Virulence Factors ,Immunology ,Virulence ,Inflammation ,Infectious and parasitic diseases ,RC109-216 ,Gut flora ,virulence factor ,Microbiology ,Virulence factor ,Type three secretion system ,medicine ,Humans ,metagenomic ,Child ,Gene ,Feces ,gut microbiota ,biology ,biology.organism_classification ,medicine.disease ,Obesity ,Diet ,Gastrointestinal Microbiome ,high-fiber diet ,Infectious Diseases ,inflammation ,Parasitology ,medicine.symptom ,Research Article ,Research Paper - Abstract
In our previous study, a gut microbiota-targeted dietary intervention with a high-fiber diet improved the immune status of both genetically obese (Prader-Willi Syndrome, PWS) and simple obese (SO) children. However, PWS children had higher inflammation levels than SO children throughout the trial, the gut microbiota of the two cohorts was similar. As some virulence factors (VFs) produced by the gut microbiota play a role in triggering host inflammation, this study compared the characteristics and changes of gut microbial VF genes of the two cohorts before and after the intervention using a fecal metagenomic dataset. We found that in both cohorts, the high-fiber diet reduced the abundance of VF, and particularly pathogen-specific, genes. The composition of VF genes was also modulated, especially for offensive and defensive VF genes. Furthermore, genes belonging to invasion, T3SS (type III secretion system), and adherence classes were suppressed. Co-occurrence network analysis detected VF gene clusters closely related to host inflammation in each cohort. Though these cohort-specific clusters varied in VF gene combinations and cascade reactions affecting inflammation, they mainly contained VFs belonging to iron uptake, T3SS, and invasion classes. The PWS group had a lower abundance of VF genes before the trial, which suggested that other factors could also be responsible for the increased inflammation in this cohort. This study provides insight into the modulation of VF gene structure in the gut microbiota by a high-fiber diet, with respect to reduced inflammation in obese children, and differences in VF genes between these two cohorts.
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- 2021
35. Probiotics Stimulate Bone Formation in Obese Mice via Histone Methylations
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Jessica Ison, Michael J. Voor, Neetu Tyagi, and Jyotirmaya Behera
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mitochondrial biogenesis ,Medicine (miscellaneous) ,Mice, Obese ,Gut flora ,Diet, High-Fat ,Methylation ,Bone and Bones ,Epigenesis, Genetic ,Histones ,Mice ,Downregulation and upregulation ,bone loss ,Osteogenesis ,RNA, Ribosomal, 16S ,Histone methylation ,medicine ,Animals ,Epigenetics ,histone methylation ,Obesity ,Pharmacology, Toxicology and Pharmaceutics (miscellaneous) ,osteoblasts mineralization ,Inflammation ,Bone Development ,biology ,gut microbiota ,Chemistry ,Probiotics ,Osteoblast ,TFAM ,biology.organism_classification ,Cell biology ,Gastrointestinal Microbiome ,Mitochondria ,Mice, Inbred C57BL ,medicine.anatomical_structure ,Mitochondrial biogenesis ,biology.protein ,Demethylase ,Dysbiosis ,Female ,Insulin Resistance ,Research Paper - Abstract
Rationale: Manipulation of the gut microbiome can prevent pathologic bone loss. However, the effects of probiotics on mitochondrial epigenetic remodeling and skeletal homeostasis in the high-fat diet (HFD)-linked obesity remains to be explored. Here, we examined the impact of probiotics supplementation on mitochondrial biogenesis and bone homeostasis through the histone methylation mechanism in HFD fed obese mice. Methods: 16S rRNA gene sequencing was performed to study the microbiota composition in the gut and microbial dysbiosis in obese mouse model. High resolution (microPET/CT) imaging was performed to demonstrate the obese associated colonic inflammation. Obese-associated upregulation of target miRNA in osteoblast was investigated using a microRNA qPCR array. Osteoblastic mitochondrial mass was evaluated using confocal imaging. Overexpression of mitochondrial transcription factor (Tfam) was used to investigate the glycolysis and mitochondrial bioenergetic metabolism using Tfam-transgenic (Tg) mice fed on HFD. The bone formation and mechanical strength was evaluated by microCT analysis and three-point bending analysis. Results: High-resolution imaging (µ-CT) and mechanical testing revealed that probiotics induced a significant increase of trabecular bone volume and bone mechanical strength respectively in obese mice. Probiotics or Indole-3-propionic acid (IPA) treatment directly to obese mice, prevents gut inflammation, and improved osteoblast mineralization. Mechanistically, probiotics treatment increases mitochondrial transcription factor A (Tfam) expression in osteoblasts by promoting Kdm6b/Jmjd3 histone demethylase, which inhibits H3K27me3 epigenetic methylation at the Tfam promoter. Furthermore, Tfam-transgenic (Tg) mice, fed with HFD, did not experience obesity-linked reduction of glucose uptake, mitochondrial biogenesis and mineralization in osteoblasts. Conclusions: These results suggest that the probiotics mediated changes in the gut microbiome and its derived metabolite, IPA are potentially be a novel agent for regulating bone anabolism via the gut-bone axis.
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- 2021
36. Beyond probiotic legend: ESSAP gut microbiota health score to delineate SARS-COV-2 infection severity
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Omar Ashoush, Mohamed Tharwat Hegazy, Rania Mohamed Lithy, Mahmoud Wahba, Hoda M Abdel-Hamid, Samah Ahmed Abd Elshafy, Mona A. Hegazy, Ahmed Abdelghani, Dalia Abdelfatah, and Maha Hossam El-Din Ibrahim
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medicine.medical_specialty ,medicine.drug_class ,medicine.medical_treatment ,Antibiotics ,Medicine (miscellaneous) ,Gut microbiota ,Clinical nutrition ,Disease ,Gut flora ,law.invention ,Probiotic ,law ,Internal medicine ,medicine ,Global health ,Humans ,Longitudinal Studies ,Medical prescription ,Pandemics ,Exercise ,Nutrition and Dietetics ,biology ,SARS-CoV-2 ,business.industry ,Probiotics ,Prebiotic ,COVID-19 ,Full Papers ,biology.organism_classification ,Gastrointestinal Microbiome ,Prebiotics ,business ,Human and Clinical Nutrition - Abstract
COVID-19 pandemic continues to be a global health crisis. The gut microbiome critically affects the immune system, and some respiratory infections are associated with changes in the gut microbiome; here, we evaluated the role of nutritional and lifestyle habits that modulate gut microbiota on COVID-19 outcomes in a longitudinal cohort study that included 200 patients infected with COVID-19. Of these, 122 cases were mild and seventy-eight were moderate, according to WHO classification. After detailed explanation by a consultant in clinical nutrition, participants responded to a written questionnaire on daily sugar, prebiotic intake in food, sleeping hours, exercise duration and antibiotic prescription, during the past 1 year before infection. Daily consumption of prebiotic-containing foods, less sugar, regular exercise, adequate sleep and fewer antibiotic prescriptions led to a milder disease and rapid virus clearance. Additionally, data on these factors were compiled into a single score, the ESSAP score (Exercise, Sugar consumption, Sleeping hours, Antibiotics taken, and Prebiotics consumption; 0–11 points), median ESSAP score was 5 for both mild and moderate cases; however, the range was 4–8 in mild cases, but 1–6 in moderate (P = 0·001, OR: 4·2, 95 % CI 1·9, 9·1); our results showed a negative correlation between regular consumption of yogurt containing probiotics and disease severity (P = 0·007, OR: 1·6, 95 % CI 1·1, 2·1). Mild COVID-19 disease was associated with 10–20 min of daily exercise (P = 0·016), sleeping at least 8 h daily, prescribed antibiotics less than 5 times per year (P = 0·077) and ate plenty of prebiotic-containing food.
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- 2021
37. Cistanche deserticola polysaccharides alleviate cognitive decline in aging model mice by restoring the gut microbiota-brain axis
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Jie Gao, Yang Liu, Hong Liu, Yajuan Tian, Xiaoli Du, Ren Bu, Bing Li, Gao Yuan, Gang Li, and Chao Gu
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Aging ,medicine.medical_specialty ,Cistanche deserticola ,Inflammation ,Gut flora ,medicine.disease_cause ,chemistry.chemical_compound ,Valine ,Internal medicine ,learning and memory deterioration ,medicine ,Cognitive decline ,CDPS ,biology ,gut microbiota ,business.industry ,Cell Biology ,biology.organism_classification ,Endocrinology ,chemistry ,Uric acid ,medicine.symptom ,business ,Homeostasis ,Oxidative stress ,Research Paper - Abstract
Recent evidence suggests alterations in the gut microbiota-brain axis may drive cognitive impairment with aging. In the present study, we observed that prolonged administration of D-galactose to mice induced cognitive decline, gut microbial dysbiosis, peripheral inflammation, and oxidative stress. In this model of age-related cognitive decline, Cistanche deserticola polysaccharides (CDPS) improved cognitive function in D-galactose-treated mice by restoring gut microbial homeostasis, thereby reducing oxidative stress and peripheral inflammation. The beneficial effects of CDPS in these aging model mice were abolished through ablation of gut microbiota with antibiotics or immunosuppression with cyclophosphamide. Serum metabolomic profiling showed that levels of creatinine, valine, L-methionine, o-Toluidine, N-ethylaniline, uric acid and proline were all altered in the aging model mice, but were restored by CDPS. These findings demonstrated that CDPS improves cognitive function in a D-galactose-induced aging model in mice by restoring homeostasis of the gut microbiota-brain axis, which alleviated an amino acid imbalance, peripheral inflammation, and oxidative stress. CDPS thus shows therapeutic potential for patients with memory and learning disorders, especially those related to gut microbial dysbiosis.
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- 2021
38. Cigarette smoking status alters dysbiotic gut microbes in hypertensive patients
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Jie Jiao, Ying Dong, Pan Wang, Kun Zuo, Xinchun Yang, Jing Li, Shu Ding, Mulei Chen, Chunming Han, and Lei Zhao
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hypertension ,Endocrinology, Diabetes and Metabolism ,Phycisphaera ,cigarette smoking ,Physiology ,030204 cardiovascular system & hematology ,Gut flora ,03 medical and health sciences ,0302 clinical medicine ,Cigarette smoking ,Tobacco ,Internal Medicine ,Humans ,Medicine ,cardiovascular diseases ,030212 general & internal medicine ,Gut Microbiota ,Feces ,Original Paper ,Clostridiales ,biology ,business.industry ,medicine.disease ,biology.organism_classification ,Gastrointestinal Microbiome ,Intestinal Microbiome ,Dysbiosis ,Smoking status ,Enterotype ,Cardiology and Cardiovascular Medicine ,business - Abstract
Smoking not only is one of the most important risk factors of hypertension (HTN), but also alters the composition of gut microbiota (GM) in previous studies. Although dysbiosis of GM has been implicated in HTN, how GM alters in patients with HTN under smoking status is still not clear. This study aimed to explore the difference in intestinal microflora among smokers with HTN (S‐HTN), nonsmokers with HTN (NS‐HTN), and smokers without HTN (S‐CTR) and identify whether cigarette smoking led to disordered intestinal microbiota in patients with HTN. Metagenomic sequencing analysis of fecal specimens was conducted in nonsmokers without HTN (NS‐CTR, n = 9), S‐CTR (n = 9), NS‐HTN (n = 18), and S‐HTN (n = 23). Compared with S‐CTR or NS‐HTN, the GM in S‐HTN was disordered, with lower microbial α‐diversity and significant difference of β‐diversity on axes as compared to S‐CTR at genus and species level. The microbial enterotype in S‐HTN was inclined to Prevotella‐dominant type. Dramatic changes in the intestinal genera and species composition were observed in S‐HTN, including reduced enrichment of Phycisphaera and Clostridium asparagiforme. Moreover, the intestinal function altered in S‐HTN. Therefore, the findings of the present study revealed GM disorders in S‐HTN and clarified the role of smoking in impairing the intestinal microbiome in HTN. Tobacco control is particularly important for improving GM in patients with HTN, and might be beneficial in preventing future cardiovascular events.
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- 2021
39. Alterations in fecal short chain fatty acids (SCFAs) and branched short-chain fatty acids (BCFAs) in men with benign prostatic hyperplasia (BPH) and metabolic syndrome (MetS)
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Arnold Mizerski, Olimpia Sipak, Weronika Ratajczak, Aleksandra Rył, Małgorzata Piasecka, Marcin Słojewski, and Maria Laszczyńska
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Dietary Fiber ,Male ,Aging ,medicine.medical_specialty ,food.ingredient ,Valeric acid ,short-chain fatty acids ,Prostatic Hyperplasia ,Gut flora ,Caproic Acid ,Isobutyric acid ,Butyric acid ,Feces ,chemistry.chemical_compound ,food ,Risk Factors ,Internal medicine ,medicine ,Humans ,Intestinal Mucosa ,Resistant starch ,benign prostatic hyperplasia (BPH) ,Aged ,Metabolic Syndrome ,gut microbiota ,biology ,Cell Biology ,Middle Aged ,metabolic syndrome (MetS) ,Fatty Acids, Volatile ,medicine.disease ,biology.organism_classification ,microbiota-gut-prostate axis ,Healthy Volunteers ,Gastrointestinal Microbiome ,Endocrinology ,chemistry ,Case-Control Studies ,Benign prostatic hyperplasia (BPH) ,Metabolic syndrome ,Research Paper - Abstract
Gut microbiome-derived short-chain fatty acids (SCFAs) emerge in the process of fermentation of polysaccharides that resist digestion (dietary fiber, resistant starch). SCFAs have a very high immunomodulatory potential and ensure local homeostasis of the intestinal epithelium, which helps maintain the intestinal barrier. We analyzed the association between stool SCFAs levels acetic acid (C 2:0), propionic acid (C 3:0), isobutyric acid (C 4:0i), butyric acid (C 4:0n), isovaleric acid (C 5:0i) valeric acid (C 5:0n), isocaproic acid (C 6:0i), and caproic acid (C 6:0n)) in aging man with benign prostatic hyperplasia (BPH) and healthy controls. The study involved 183 men (with BPH, n = 103; healthy controls, n = 80). We assessed the content of SCFAs in the stool samples of the study participants using gas chromatography. The levels of branched SCFAs (branched-chain fatty acids, BCFAs): isobutyric acid (C4:0i) (p = 0.008) and isovaleric acid (C5:0i) (p < 0.001) were significantly higher in patients with BPH than in the control group. In healthy participants isocaproic acid (C6:0i) predominated (p = 0.038). We also analyzed the relationship between stool SCFA levels and serum diagnostic parameters for MetS. We noticed a relationship between C3:0 and serum lipid parameters (mainly triglycerides) in both healthy individuals and patients with BPH with regard to MetS. Moreover we noticed relationship between C4:0i, C5:0i and C6:0i and MetS in both groups. Our research results suggest that metabolites of the intestinal microflora (SCFAs) may indicate the proper function of the intestines in aging men, and increased BCFAs levels are associated with the presence of BPH.
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- 2021
40. Cohousing-mediated microbiota transfer from milk bioactive components-dosed mice ameliorate colitis by remodeling colonic mucus barrier and lamina propria macrophages
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Dandan Han, Shilan Wang, Zhenhua Wu, Na Li, Bing Zhang, Cong Liu, Shimeng Huang, Jiangchao Zhao, Junjun Wang, and Tiantian Li
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0301 basic medicine ,colitis ,CMFG ,Oligosaccharides ,RC799-869 ,Gut flora ,Mice ,0302 clinical medicine ,RNA, Ribosomal, 16S ,Homeostasis ,biology ,medicine.diagnostic_test ,Dextran Sulfate ,Gastroenterology ,intestinal homeostasis ,Diseases of the digestive system. Gastroenterology ,cohousing ,Infectious Diseases ,medicine.anatomical_structure ,Cytokines ,030211 gastroenterology & hepatology ,Female ,Infiltration (medical) ,Research Article ,Research Paper ,Microbiology (medical) ,Colon ,Breast milk ,Microbiology ,digestive system ,Flow cytometry ,03 medical and health sciences ,Exome Sequencing ,medicine ,Animals ,Humans ,Colitis ,Gene ,Glycoproteins ,Lamina propria ,Mucous Membrane ,gut microbiota ,Milk, Human ,Macrophages ,Lipid Droplets ,medicine.disease ,biology.organism_classification ,Fatty Acids, Volatile ,Gastrointestinal Microbiome ,Mice, Inbred C57BL ,Disease Models, Animal ,Mucus ,030104 developmental biology ,Dysbiosis ,Glycolipids - Abstract
Human milk oligosaccharides (HMOs) and milk fat globule membrane (MFGM) are highly abundant in breast milk, and have been shown to exhibit potent immunomodulatory effects. Yet, their role in the gut microbiota modulation in relation to colitis remains understudied. Since the mixtures of fructo-oligosaccharides (FOS) and galacto-oligosaccharides (GOS) perfectly mimic the properties and functions of HMOs, the combination of MFGM, FOS, and GOS (CMFG) has therefore been developed and used in this study. Here, CMFG were pre-fed to mice for three weeks to investigate its preventive effect on dextran sodium sulfate (DSS) induced colitis. Moreover, CMFG-treated and vehicle-treated mice were cohoused to further elucidate the preventive role of the gut microbiota transfer in colitis. At the end of the study, 16S rDNA gene amplicon sequencing, short-chain fatty acids (SCFAs) profiling, transcriptome sequencing, histological analysis, immunofluorescence staining and flow cytometry analysis were conducted. Our results showed that CMFG pre-supplementation alleviated DSS-induced colitis as evidenced by decreased disease activity index (DAI) score, reduced body weight loss, increased colon length and mucin secretion, and ameliorated intestinal damage. Moreover, CMFG reduced macrophages in the colon, resulting in decreased levels of IL-1β, IL-6, IL-8, TNF-α, and MPO in the colon and circulation. Furthermore, CMFG altered the gut microbiota composition and promoted SCFAs production in DSS-induced colitis. Markedly, the cohousing study revealed that transfer of gut microbiota from CMFG-treated mice largely improved the DSS-induced colitis as evidenced by reduced intestinal damage and decreased macrophages infiltration in the colon. Moreover, transfer of the gut microbiota from CMFG-treated mice protected against DSS-induced gut microbiota dysbiosis and promotes SCFAs production, which showed to be associated with colitis amelioration. Collectively, these findings demonstrate the beneficial role of CMFG in the gastrointestinal diseases, and further provide evidence for the rational design of effective prophylactic functional diets in both animals and humans.
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- 2021
41. Limosilactobacillus fermentum JL-3 isolated from 'Jiangshui' ameliorates hyperuricemia by degrading uric acid
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Xiangkai Li, Apurva Kakade, Rong Li, Pengya Feng, Xiao Chen, Pu Liu, Xiaozhu Tian, Ying Wu, Rong Han, and Ze Ye
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musculoskeletal diseases ,0301 basic medicine ,Microbiology (medical) ,congenital, hereditary, and neonatal diseases and abnormalities ,RC799-869 ,Hyperuricemia ,Gut flora ,urologic and male genital diseases ,Microbiology ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,gout ,uric acid ,medicine ,Food science ,Beneficial effects ,Fermentation in food processing ,biology ,gut microbiota ,limosilactobacillus fermentum ,digestive, oral, and skin physiology ,Gastroenterology ,nutritional and metabolic diseases ,Diseases of the digestive system. Gastroenterology ,biology.organism_classification ,medicine.disease ,Gout ,030104 developmental biology ,Infectious Diseases ,chemistry ,Uric acid ,030211 gastroenterology & hepatology ,Research Article ,Research Paper - Abstract
Recent studies into the beneficial effects of fermented foods have shown that this class of foods are effective in managing hyperuricemia and gout. In this study, the uric acid (UA) degradation ability of Limosilactobacillus fermentum JL-3 strain, isolated from “Jiangshui” (a fermented Chinese food), was investigated. In vitro results showed that JL-3 strain exhibited high degradation capacity and selectivity toward UA. After oral administration to mice for 15 days, JL-3 colonization was continuously detected in the feces of mice. The UA level in urine of mice fed with JL-3 was similar with the control group mice. And the serum UA level of the former was significantly lower (31.3%) than in the control, further confirmed the UA-lowering effect of JL-3 strain. Limosilactobacillus fermentum JL-3 strain also restored some of the inflammatory markers and oxidative stress indicators (IL-1β, MDA, CRE, blood urea nitrogen) related to hyperuricemia, while the gut microbial diversity results showed that JL-3 could regulate gut microbiota dysbiosis caused by hyperuricemia. Therefore, the probiotic Limosilactobacillus fermentum JL-3 strain is effective in lowering UA levels in mice and could be used as a therapeutic adjunct agent in treating hyperuricemia.
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- 2021
42. Gut microbiota in insulin resistance: a bibliometric analysis
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Tian, Weiwei, Liu, Li, Wang, Ruirui, Quan, Yunyun, Tang, Bihua, Yu, Dongmei, Zhang, Lei, Hua, Hua, and Zhao, Junning
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- 2024
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43. Indoxyl sulfate caused behavioral abnormality and neurodegeneration in mice with unilateral nephrectomy
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Shih-Yi Lin, Su-Lan Liao, Jian-Ri Li, Cheng-Jui Lin, Jiaan-Der Wang, Yen-Chuan Ou, Chiao-Yin Sun, Chun-Jung Chen, and Ya-Yu Wang
- Subjects
Male ,Aging ,Interleukin-1beta ,uremic toxin ,Anxiety ,Gut flora ,medicine.disease_cause ,Nephrectomy ,neuroinflammation ,Neural Stem Cells ,Neurotrophic factors ,Behavior, Animal ,biology ,Depression ,Neurodegeneration ,neurodegeneration ,Oxides ,medicine.anatomical_structure ,Injections, Intraperitoneal ,Research Paper ,Serotonin ,medicine.medical_specialty ,Cell Survival ,Neurogenesis ,Central nervous system ,Prefrontal Cortex ,Internal medicine ,medicine ,Animals ,Cognitive Dysfunction ,RNA, Messenger ,Renal Insufficiency, Chronic ,Neuroinflammation ,gut microbiota ,business.industry ,Brain-Derived Neurotrophic Factor ,Cell Biology ,medicine.disease ,Aryl hydrocarbon receptor ,biology.organism_classification ,Carbon ,Mice, Inbred C57BL ,Repressor Proteins ,Affect ,Oxidative Stress ,Endocrinology ,biology.protein ,Corticosterone ,business ,Indican ,Oxidative stress ,Kidney disease - Abstract
Chronic Kidney Disease (CKD) and neurodegenerative diseases are aging-related diseases. CKD with declined renal function is associated with an elevation of circulating indoxyl sulfate, a metabolite synthesized by gut microbes. We explored the roles of gut microbial metabolites in linking with Central Nervous System (CNS) diseases by administrating indoxyl sulfate intraperitoneally to male C57BL/6 mice with unilateral nephrectomy. Upon exposure, the accumulation of indoxyl sulfate was noted in the blood, prefrontal cortical tissues, and cerebrospinal fluid. Mice showed behavioral signs of mood disorders and neurodegeneration such as anxiety, depression, and cognitive impairment. Those behavioral changes were accompanied by disturbed neuronal survival, neural stem cell activity, expression of Brain-Derived Neurotrophic Factor, serotonin, corticosterone, and Repressor Element-1 Silencing Transcription Factor, and post-receptor intracellular signaling, as well as upregulated oxidative stress and neuroinflammation. Uremic toxin adsorbent AST-120 improved the above mentioned changes. Intriguingly, intracerebroventricular indoxyl sulfate administration only caused limited alterations in the normal mice and the alterations were reversed by aryl hydrocarbon receptor antagonism. The findings suggest pathogenic roles of indoxyl sulfate in the development of CNS diseases, and highlight gut microbiota as alternative targets for intervention with the aim of slowing down the progression of CKD and decreasing CNS complications.
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- 2021
44. The rectal mucosal but not fecal microbiota detects subclinical ulcerative colitis
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Cheng-Yu Lin, Wei-An Liu, Yu-Fei Lin, Chia-Jung Kuo, Huei-Mien Ke, Chang Mu Sung, Sen-Yung Hsieh, Hao-Tsai Cheng, Wen-Sy Tsai, Mei-Yeh Jade Lu, and Isheng J. Tsai
- Subjects
0301 basic medicine ,Microbiology (medical) ,subclinical UC detection ,Adult ,Male ,RC799-869 ,Gut microbiota ,Gut flora ,Microbiology ,Inflammatory bowel disease ,Pathogenesis ,03 medical and health sciences ,Feces ,0302 clinical medicine ,inflammatory bowel disease ,medicine ,Humans ,Intestinal Mucosa ,Cecum ,Subclinical infection ,ulcerative colitis ,biology ,digestive, oral, and skin physiology ,Gastroenterology ,Rectum ,Diseases of the digestive system. Gastroenterology ,Fecal microbiota ,Middle Aged ,medicine.disease ,biology.organism_classification ,Ulcerative colitis ,digestive system diseases ,Gut microbiome ,Gastrointestinal Microbiome ,030104 developmental biology ,Infectious Diseases ,Immunology ,rectal biopsy microbiome ,Dysbiosis ,030211 gastroenterology & hepatology ,Colitis, Ulcerative ,Female ,Research Article ,Research Paper - Abstract
Ulcerative colitis (UC), a subtype of inflammatory bowel disease, is characterized by repetitive remission and relapse. Gut microbiome is critically involved in pathogenesis of UC. The shifts in microbiome profile during disease remission remain under-investigated. Recent studies revealed that UC pathogenesis is likely to originate in the mucosal barrier. Therefore, we investigated the effectiveness of mucosal tissue microbiomes to differentiate patients with subclinical UC from healthy individuals. The microbiomes of cecal and rectal biopsies and feces were characterized from 13 healthy individuals and 45 patients with subclinical UC. Total genomic DNA was extracted from the samples, and their microbial communities determined using next-generation sequencing. We found that changes in relative abundance of subclinical UC were marked by a decrease in Proteobacteria and an increase in Bacteroidetes phyla in microbiome derived from rectal tissues but not cecal tissue nor feces. Only in the microbiome of rectal tissue had significantly higher community richness and evenness in subclinical UC patients than controls. Twenty-seven operational taxonomic units were enriched in subclinical UC cohort with majority of the taxa from the Firmicutes phylum. Inference of putative microbial functional pathways from rectal biopsy microbiome suggested a differential increase in interleukin-17 signaling and T-helper cell differentiation pathways. Rectal biopsy tissue was suggested to be more suitable than fecal samples for microbiome assays to distinguish patients with subclinical UC from healthy adults. Assessment of the rectal biopsy microbiome may offer clinical insight into UC disease progression and predict relapse of the diseases.
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- 2021
45. Bovine serum albumin aggravates macrophage M1 activation and kidney injury in heterozygous Klotho-deficient mice via the gut microbiota-immune axis
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Lingyun Lai, Jun Xue, Te Liu, Jianjun Liu, Jianguo Tang, Yi Li, and Lei Luo
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Male ,medicine.medical_specialty ,Inflammation ,Applied Microbiology and Biotechnology ,Klotho ,Superoxide dismutase ,03 medical and health sciences ,Mice ,Immune system ,Western blot ,Fibrosis ,Internal medicine ,medicine ,Animals ,Bovine serum albumin ,Renal Insufficiency, Chronic ,Molecular Biology ,Klotho Proteins ,Ecology, Evolution, Behavior and Systematics ,030304 developmental biology ,0303 health sciences ,medicine.diagnostic_test ,biology ,gut microbiota ,Chemistry ,Lipid metabolism ,Serum Albumin, Bovine ,Cell Biology ,Macrophage Activation ,medicine.disease ,Gastrointestinal Microbiome ,Endocrinology ,Nrf2/NF-κB pathway ,macrophage M1 ,biology.protein ,kidney injury ,medicine.symptom ,Developmental Biology ,Research Paper - Abstract
Klotho expression abnormalities induces kidney injury and chronic kidney disease, however, the underlying mechanism remains unclear. Here, Klotho+/- mice and wild-type mice were treated with low-dose bovine serum albumin (BSA). Pathological examination demonstrated that the area of glomerular collagen deposition and fibrosis in BSA-Kl-/+ mice was significantly larger than that in BSA-WT mice. The serum levels of superoxide dismutase, malondialdehyde, creatinine, and urea in BSA-Kl-/+ mice were significantly increased. Sequencing of gut microbiota 16S rRNA v3-v4 region indicated that BSA-Kl-/+ mice showed a significantly higher relative abundance of the genera Dubosiella, Akkermansia, Alloprevotella, and Lachnospiraceae and a significantly lower relative abundance of the genera Allobaculum and Muribaculaceae than BSA-WT mice. KEGG analysis revealed that the metabolic pathways of signal transduction, xenobiotic biodegradation and metabolism, and lipid metabolism increased significantly in BSA-Kl-/+ mice. Flow cytometry showed that the proportion of CD68+/CD11b+ cells in the peripheral blood was significantly higher in BSA-KL-/+ mice than that in BSA-WT mice. qPCR and western blot suggested that Klotho and Nrf2 expression in MΦ1 cells of BSA-KL-/+ mice was significantly decreased. Thus, the findings suggest during the immune activation and chronic inflammation induced by the gut microbiota imbalance in Klotho-deficient mice treated to BSA, disrupted expression of proteins in the Nrf2/NF-κB signaling pathway in monocyte-derived macrophage M1 cells leads to the aggravation of inflammation and kidney injury.
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- 2021
46. Fecal microbiota transplantation mitigates vaginal atrophy in ovariectomized mice
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Fuxia Li, Ensong Guo, Jing Cheng, Ling Xi, Shixuan Wang, Jia Huang, Bin Yang, Xi Li, Funian Lu, Rourou Xiao, Chen Liu, Ding Ma, Rajluxmee Beejadhursing, Yu Fu, Wanying Shan, Chaoyang Sun, Zizhuo Wang, and Gang Chen
- Subjects
Aging ,medicine.drug_class ,medicine.medical_treatment ,Ovariectomy ,Physiology ,Gut flora ,digestive system ,genitourinary syndrome of menopause ,vulvovaginal atrophy ,Mice ,RNA, Ribosomal, 16S ,medicine ,Animals ,Feces ,biology ,gut microbiota ,business.industry ,Cancer ,Cell Biology ,Fecal Microbiota Transplantation ,medicine.disease ,biology.organism_classification ,Gastrointestinal Microbiome ,Mice, Inbred C57BL ,medicine.anatomical_structure ,Estrogen ,vaginal epithelium ,Vagina ,Ovariectomized rat ,ovariectomized mouse model ,Female ,Vaginal atrophy ,Hormone therapy ,Atrophy ,business ,Research Paper - Abstract
Vulvovaginal atrophy (VVA) is a common menopause-related symptom affecting more than 50% of midlife and older women and cancer patients whose ovarian function are lost or damaged. Regardless of estrogen deficiency, whether other factors such as the gut microbiota play role in VVA have not been thoroughly investigated. To this end, we performed ovariectomy on 12-weeks' old mice and follow-up at 4 weeks after ovariectomy, and observed atrophied vagina and an altered gut microbiota in ovariectomized mice.. We further performed fecal microbiota transplantation with feces from another cohort of ovary-intact fecund female mice to the ovariectomized ones, and found that the vaginal epithelial atrophy was significantly alleviated as well as the gut microbiota was pointedly changed. All these results suggest that ovarian activity has some influence on the gut microbiota, and the latter from the ovary-intact female mice can somehow make the vagina of mice deficient in ovarian function healthier maybe by up-expressing ESR1 in vaginal cells and enhancing regeneration in vagina. This kind of association between gut microbiota and vaginal health need further exploration such that it may provide an alternative treatment by modulating gut microbiota in patients suffering from VVA but may be reluctant to hormone therapy.
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- 2021
47. Compensatory intestinal immunoglobulin response after vancomycin treatment in humans
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Max Nieuwdorp, Guido J. Bakker, Daniël H. van Raalte, Hilde Herrema, Maaike Winkelmeijer, Torsten P. M. Scheithauer, Mark Davids, IOO, Internal medicine, ACS - Diabetes & metabolism, AGEM - Endocrinology, metabolism and nutrition, Amsterdam Gastroenterology Endocrinology Metabolism, Vascular Medicine, Experimental Vascular Medicine, and Center of Experimental and Molecular Medicine
- Subjects
0301 basic medicine ,Microbiology (medical) ,Adult ,Lipopolysaccharides ,Male ,LPS ,Lipopolysaccharide ,Adolescent ,vancomycin ,Immunoglobulins ,RC799-869 ,Gut flora ,Microbiology ,flagellin ,Bacterial cell structure ,03 medical and health sciences ,chemistry.chemical_compound ,Feces ,Young Adult ,0302 clinical medicine ,Immune system ,Gram-Negative Bacteria ,medicine ,Immunoglobulin ,Humans ,Aged ,Metabolic Syndrome ,biology ,gut microbiota ,Gastroenterology ,Diseases of the digestive system. Gastroenterology ,Middle Aged ,biology.organism_classification ,Healthy Volunteers ,Gastrointestinal Microbiome ,Intestines ,030104 developmental biology ,Infectious Diseases ,chemistry ,biology.protein ,Vancomycin ,030211 gastroenterology & hepatology ,Antibody ,Flagellin ,Bacteria ,medicine.drug ,Research Article ,Research Paper - Abstract
Intestinal immunoglobulins (Ig) are abundantly secreted antibodies that bind bacteria and bacterial components in the gut. This binding is considered to accelerate bacterial transit time and prevent the interaction of potentially immunogenic compounds with intestinal immune cells. Ig secretion is regulated by alterations in gut microbiome composition, an event rarely mapped in an intervention setting in humans. Here, we determined the intestinal and systemic Ig response to a major intervention in gut microbiome composition. Healthy humans and humans with metabolic syndrome received oral vancomycin 500 mg four times per day for 7 days. Coinciding with a vancomycin-induced increase in Gram-negative bacteria, fecal levels of the immunogenic bacterial components lipopolysaccharide (LPS) and flagellin drastically increased. Intestinal antibodies (IgA and IgM) significantly increased, whereas peripheral antibodies (IgG, IgA, and IgM) were mostly unaffected by vancomycin treatment. Bacterial cell sorting followed by 16S rRNA sequencing revealed that the majority of Gram-negative bacteria, including opportunistic pathogens, were IgA-coated after the intervention. We suggest that the intestinal Ig response after vancomycin treatment prevents the intrusion of pathogens and bacterial components into systemic sites.
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- 2021
48. Profile of gut microbiota in patients with traumatic thoracic spinal cord injury and its clinical implications: a case-control study in a rehabilitation setting
- Author
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Caiyun Zhong, Huaide Qiu, Binbin Yu, Feng Ye, Shupeng Cheng, Chen Sijing, Yumei Yang, Jianan Li, Zhou Li, and Jiahui Li
- Subjects
Adult ,medicine.medical_specialty ,Adolescent ,medicine.medical_treatment ,serum biomarkers ,Bioengineering ,Gut microbiota ,traumatic thoracic spinal cord injury ,Gut flora ,digestive system ,Applied Microbiology and Biotechnology ,Gastroenterology ,Thoracic Vertebrae ,Feces ,Young Adult ,Neurogenic Bowel ,Serum biomarkers ,Internal medicine ,medicine ,Humans ,In patient ,Spinal cord injury ,Spinal Cord Injuries ,Aged ,Rehabilitation ,biology ,business.industry ,Case-control study ,General Medicine ,Middle Aged ,biology.organism_classification ,medicine.disease ,Gastrointestinal Microbiome ,Case-Control Studies ,neurogenic bowel dysfunction ,Dysbiosis ,business ,TP248.13-248.65 ,Biomarkers ,Research Article ,Research Paper ,Biotechnology ,Thoracic spinal cord injury - Abstract
Gut microbiota are the candidate biomarkers for neurogenic bowel dysfunction (NBD) in patients with spinal cord injury (SCI). We aimed to identify the common features between patients with varying degree of thoracic SCI and healthy individuals and subpopulations of microbiota correlated with the serum biomarkers. Twenty-one patients with complete thoracic SCI (CTSCI), 24 with incomplete thoracic SCI (ITSCI), and 24 healthy individuals (HC) were enrolled in this study. Fresh stool samples and clinical data were collected from all participants, and their bowel functions with SCI were assessed. Microbial diversity and composition were analyzed by sequencing the 16S rRNA gene. The features of gut microbiota correlated with the serum biomarkers and their functions were investigated. The mean NBD score of patients with CTSCI was higher than that of patients with ITSCI. Diversity of the gut microbiota in SCI group was reduced, and with an increase in the degree of damage, alpha diversity had decreased gradually. The composition of gut microbiota in patients with SCI was distinct from that in healthy individuals, and CTSCI group exhibited further deviation than ITSCI group compared to healthy individuals. Four serum biomarkers were found to be correlated with most differential genera. Patients with thoracic SCI present gut dysbiosis, which is more pronounced in patients with CTSCI than in those with ITSCI. Therefore, the gut microbiota profile may serve as the signatures for bowel and motor functions in patients with thoracic SCI., GRAPHICAL ABSTRACT
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- 2021
49. The Association of Targeted Gut Microbiota with Body Composition in Type 2 Diabetes Mellitus
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Mei-Chuan Kuo, Chia-Yen Dai, Shang-Jyh Hwang, Chen-Chia Chang, Szu-Chia Chen, Hui-Ju Tsai, Yi-Wen Chiu, Wei-Chun Hung, Wei-Wen Hung, and Yi-Chun Tsai
- Subjects
DNA, Bacterial ,Male ,Firmicutes ,Faecalibacterium prausnitzii ,Gut flora ,Microbiology ,03 medical and health sciences ,0302 clinical medicine ,Risk Factors ,RNA, Ribosomal, 16S ,Type 2 diabetes mellitus ,Prevalence ,Humans ,Aged ,gut microbiota ,biology ,Bacteroidetes ,Clostridium leptum ,Type 2 Diabetes Mellitus ,General Medicine ,Middle Aged ,biology.organism_classification ,Gastrointestinal Microbiome ,Diabetes Mellitus, Type 2 ,Body Composition ,Dysbiosis ,bacteria ,Female ,030211 gastroenterology & hepatology ,lean tissue index ,Bacteroides ,Akkermansia muciniphila ,Research Paper - Abstract
The association between body composition and gut microbiota in type 2 diabetes mellitus (DM) remains unknown. To elucidate the correlation of body composition and gut microbiota, we conducted a clinical study to enroll 179 patients with type 2 DM. Body composition of lean tissue index (LTI) and fat tissue index was measured by Body Composition Monitor. Eight pairs of 16S rRNA gene primers specific to Firmicutes, Bacteroidetes, the Clostridium leptum group, Bacteroides, Bifidobacterium, Akkermansia muciniphila, Escherichia coli, and Faecalibacterium prausnitzii were used to measure their abundance by quantitative polymerase chain reaction. The results showed that type 2 DM with higher abundance of phylum Firmicutes and a higher ratio of phyla Firmicutes to Bacteroidetes (phyla F/B ratio) had higher LTI. This significant correlation between phyla F/B ratio and LTI was especially evident in type 2 DM with high body mass index, and independent of glycemic control or dipeptidyl peptidase-4 inhibitor usage. In conclusion, our study demonstrated the positive association of LTI with the abundance of phylum Firmicutes and the phyla F/B ratio in type 2 DM.
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- 2021
50. Pectin supplement significantly enhanced the anti-PD-1 efficacy in tumor-bearing mice humanized with gut microbiota from patients with colorectal cancer
- Author
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Chao-Yue Kong, Li-Shun Wang, Pei-Ran Cai, Zheng-Yan Zhang, Shi-Long Zhang, Zhan-Ming Li, Yu-Qin Mao, Hui-Ling Chen, Tao Ye, and Bing Han
- Subjects
Male ,0301 basic medicine ,medicine.medical_treatment ,Programmed Cell Death 1 Receptor ,programmed death-1 monoclonal antibody ,Medicine (miscellaneous) ,colorectal cancer ,Butyrate ,CD8-Positive T-Lymphocytes ,Gut flora ,Pharmacology ,Flow cytometry ,Feces ,Mice ,03 medical and health sciences ,0302 clinical medicine ,Immune system ,In vivo ,Cell Line, Tumor ,RNA, Ribosomal, 16S ,Tumor Microenvironment ,medicine ,Animals ,Humans ,Pharmacology, Toxicology and Pharmaceutics (miscellaneous) ,Aged ,pectin ,Tumor microenvironment ,gut microbiota ,Bacteria ,biology ,medicine.diagnostic_test ,Chemistry ,digestive, oral, and skin physiology ,Antibodies, Monoclonal ,Immunotherapy ,butyrate ,Fatty Acids, Volatile ,biology.organism_classification ,Gastrointestinal Microbiome ,Mice, Inbred C57BL ,030104 developmental biology ,030220 oncology & carcinogenesis ,Pectins ,Female ,Colorectal Neoplasms ,CD8 ,Research Paper - Abstract
Background: Anti-PD-1-based immunotherapy has emerged as a promising therapy for several cancers. However, it only benefits a small subset of colorectal cancer (CRC) patients. Mounting data supports the pivotal role of gut microbiota in shaping immune system. Pectin, a widely consumed soluble fiber, has been reported to ameliorate the imbalance of gut microbiota. Therefore, we aimed to explore the effect and the underlying mechanisms of pectin in improving anti-PD-1 mAb efficacy. Methods: The C57BL/6 mice were treated with a broad-spectrum antibiotic (ATB) cocktail to depleted endogenous gut microbiota and subsequently humanized with feces from healthy controls or newly diagnosed CRC patients. The antitumor efficacies of anti-PD-1 mAb combined with or without pectin were assessed using these mice. Flow cytometry and immunohistochemistry (IHC) were conducted to investigate the tumor immune microenvironment after treatment. The gut microbiota profiles and short-chain fatty acids (SCFAs) levels were determined by 16S ribosomal RNA (16S rRNA) gene sequencing and gas chromatography-mass spectrometry (GC-MS), respectively. The effect of gut microbiota on anti-PD-1 mAb efficacy after pectin supplement was further tested by fecal microbiota transplantation (FMT). Results: The anti-PD-1 mAb efficacy was largely impaired in the mice humanized with feces from newly diagnosed CRC patients compared to those from healthy controls. However, pectin significantly enhanced the anti-PD-1 mAb efficacy in the tumor-bearing mice humanized with CRC patient gut microbiota. Flow cytometry and IHC analysis revealed increased T cell infiltration and activation in the tumor microenvironment of mice treated with anti-PD-1 mAb plus pectin. In vivo depletion of CD8+ T cells diminished the anti-tumor effect of anti-PD-1 mAb combined with pectin. 16S rRNA gene sequencing showed that pectin significantly increased gut microbial diversity and beneficially regulated microbial composition. In addition, we identified unique bacterial modules that were significantly enriched in the anti-PD-1 mAb + pectin group, which composed of butyrate-producing bacteria indicative of good response to immunotherapy. Meanwhile, GC-MS showed that pectin altered the level of SCFA butyrate. Furthermore, butyrate, a main product of dietary fiber in gut microbial fermentation, was found to be sufficient to promote T cells infiltration and thus enhance the efficacy of anti-PD-1 mAb. In addition, FMT demonstrated the effects of pectin were dependent on gut microbiota. Importantly, the beneficial effects of pectin were confirmed in the mice humanized with gut microbiota from patient with resistance to anti-PD-1 mAb. Conclusion: Pectin facilitated the anti-PD-1 mAb efficacy in CRC via regulating the T cell infiltration in the tumor microenvironment, which was potentially mediated by the metabolite butyrate.
- Published
- 2021
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