8 results on '"Xiaoting Yan"'
Search Results
2. Development of Novel (+)-Nootkatone Thioethers Containing 1,3,4-Oxadiazole/Thiadiazole Moieties as Insecticide Candidates against Three Species of Insect Pests
- Author
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Ruige Yang, Meiyue Han, Jiangping Fan, Wanqing Cheng, Nannan Ma, Xiaoting Yan, and Yong Guo
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Polycyclic Sesquiterpenes ,Insecticides ,Oxadiazoles ,Structure-Activity Relationship ,Molecular Structure ,Larva ,Thiadiazoles ,Animals ,General Chemistry ,Moths ,Sulfides ,General Agricultural and Biological Sciences - Abstract
To improve the insecticidal activity of (+)-nootkatone, a series of 42 (+)-nootkatone thioethers containing 1,3,4-oxadiazole/thiadiazole moieties were prepared to evaluate their insecticidal activities against
- Published
- 2021
3. Development of Membrane-Active Honokiol/Magnolol Amphiphiles as Potent Antibacterial Agents against Methicillin-Resistant
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Yong, Guo, Enhua, Hou, Tingyu, Wen, Xiaoting, Yan, Meiyue, Han, Li-Ping, Bai, Xiangjing, Fu, Jifeng, Liu, and Shangshang, Qin
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Methicillin-Resistant Staphylococcus aureus ,Mice ,Mice, Inbred BALB C ,Structure-Activity Relationship ,Surface-Active Agents ,Drug Design ,Biphenyl Compounds ,Animals ,Microbial Sensitivity Tests ,Staphylococcal Infections ,Lignans ,Anti-Bacterial Agents - Abstract
Currently, infections caused by drug-resistant bacteria have become a new challenge in anti-infective treatment, seriously endangering public health. In our continuous effort to develop new antimicrobials, a series of novel honokiol/magnolol amphiphiles were prepared by mimicking the chemical structures and antibacterial properties of cationic antimicrobial peptides. Among them, compound
- Published
- 2021
4. Co-exposure to fluoride and arsenic disrupts intestinal flora balance and induces testicular autophagy in offspring rats
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Xiaolin Tian, Jiyu Yuan, Yulan Qiu, Fengjie Tian, Xiaoyan Yan, Ran Li, Xiaoting Yan, Meng Wang, Meng Li, Yi Lyu, Yannan Zhao, Qian Zhao, Jiaxin Xie, Cailing Wei, Xiaodong Ying, and Penghui Liu
- Subjects
Male ,medicine.medical_specialty ,Offspring ,Health, Toxicology and Mutagenesis ,chemistry.chemical_element ,Environmental pollution ,Arsenic ,Rats, Sprague-Dawley ,Fluorides ,chemistry.chemical_compound ,Intestinal flora ,Pregnancy ,Internal medicine ,Testis ,Autophagy ,medicine ,Animals ,GE1-350 ,Fluoride ,Feces ,Testosterone ,Chemistry ,Public Health, Environmental and Occupational Health ,General Medicine ,Pollution ,Gastrointestinal Microbiome ,Rats ,Environmental sciences ,Endocrinology ,TD172-193.5 ,Female ,Luteinizing hormone ,Reproductive toxicity ,Hormone - Abstract
While numerous studies have shown that fluoride or arsenic exposure may damage the reproductive system, there are few reports of co-exposure to fluoride and arsenic. In addition, the literature on autophagy and intestinal flora composition in reproductive toxicity studies of co-exposure to fluoride and arsenic is insufficient. In this study, we developed a rat model of fluoride and arsenic exposure via drinking water from pre-pregnancy to 90 days postnatal. Sprague-Dawley rats were randomly divided into sterile water control group, fluoride group (100 mg/L NaF), arsenic group (50 mg/L NaAsO2) and combined exposure group (100 mg/L NaF+50 mg/L NaAsO2). Our results showed that fluoride and arsenic exposure caused a reduction in testicular weight and significant pathological damage to tissue. We found that the levels of follicle-stimulating hormone, luteinizing hormone, and testosterone were reduced to varying degrees. Meanwhile experiments showed that fluoride and arsenic exposure can modulate autophagic flux, causing increased levels of Beclin1 and LC3 expression and decreased p62 expression. Analogously, by performing 16S sequencing of rat feces, we found 24 enterobacterial genera that differed significantly among the groups. Furthermore, the flora associated with testicular injury were identified by correlation analysis of hormonal indices and autophagy alterations with intestinal flora composition at the genus level, respectively. In summary, our study shows that fluoride and arsenic co-exposure alters autophagic flux in the testis, causes testicular injury, and reveals an association between altered intestinal flora composition and testicular injury.
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- 2021
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5. Bacterial communities in the solid, liquid, dorsal, and ventral epithelium fractions of yak ( Bos grunniens ) rumen
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Ruijun Long, Qingmiao Ren, Chang Liu, Xiaoting Yan, Qiang Qiu, Huazhe Si, Zhipeng Li, and Luming Ding
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Rikenellaceae ,Howardella spp ,lcsh:QR1-502 ,solid and liquid ,Prevotellaceae ,Real-Time Polymerase Chain Reaction ,Microbiology ,lcsh:Microbiology ,Rumen ,Fibrobacter ,Campylobacter spp ,RNA, Ribosomal, 16S ,Prevotella ,medicine ,Animals ,Bos grunniens ,rumen ,biology ,Microbiota ,Lachnospiraceae ,Computational Biology ,High-Throughput Nucleotide Sequencing ,Original Articles ,Biodiversity ,Sequence Analysis, DNA ,biology.organism_classification ,dorsal and ventral epithelium ,Epithelium ,ecology niches ,medicine.anatomical_structure ,Gastric Mucosa ,Metagenome ,Original Article ,Cattle ,Metagenomics ,Ruminococcaceae - Abstract
Yak (Bos grunniens) is an important and dominant livestock species in the challenging environment of the Qinghai–Tibetan Plateau. Rumen microbiota of the solid, liquid, and epithelium fractions play key roles in nutrient metabolism and contribute to host adaptation in ruminants. However, there is a little knowledge of the microbiota in these rumen fractions of yak. Therefore, we collected samples of solid, liquid, dorsal, and ventral epithelium fractions from five female yaks, then amplified bacterial 16S rRNA gene V4 regions and sequenced them using an Illumina MiSeq platform. Principal coordinates analysis detected significant differences in bacterial communities between the liquid, solid, and epithelium fractions, and between dorsal and ventral epithelium fractions. Rikenellaceae RC9, the families Lachnospiraceae and Ruminococcaceae, and Fibrobacter spp. were the abundant and enriched bacteria in solid fraction, while the genera Prevotella and Prevotellaceae UCG 003 were higher in the liquid fraction. Campylobacter spp., Comamonas spp., Desulfovibrio spp., and Solobacterium spp. were significantly higher in dorsal epithelium, while Howardella spp., Prevotellaceae UCG 001, Ruminococcaceae UCG 005, and Treponema 2 were enriched in the ventral epithelium. Comparison of predictive functional profiles among the solid, liquid, and dorsal, and ventral epithelium fractions also revealed significant differences. Microbiota in the ventral fraction of yak rumen also significantly differ from reported microbiota of cattle. In conclusion, our results improve our knowledge of the taxonomic composition and roles of yak rumen microbiota., In this present study, we explored microbiota in the solid, liquid, and epithelium (dorsal and ventral) fractions of yak rumen, and compared functional profiles of microbiota of the four fractions, and also compared microbiota of the ventral epithelium between yak and cattle. Our results indicated the significant differences in bacterial communities between the liquid, solid, and epithelium fractions, and between dorsal and ventral epithelium fractions. Moreover, comparison of functional profiles among the solid, liquid, and dorsal and ventral epithelium fractions also revealed significant differences. Finally, we found that the microbial composition and functional profile in the ventral epithelium between yak and cattle significantly differed, suggesting the specific role of microbiota in the ventral epithelium of yak rumen.
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- 2019
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6. ITRAQ-based proteomics reveals the potential mechanism of fluoride-induced myocardial contraction function damage
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Yi Lyu, Yannan Zhao, Jing Feng, Xiaoyan Yan, Guohua Song, Xiaoting Yan, Jiaxin Xie, Tong Wang, Cailing Wei, Penghui Liu, Guoqiang Xu, Xiaolin Tian, Guijin Ma, Nisha Dong, and Meng Li
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Male ,Proteomics ,Cardiac function curve ,Contraction (grammar) ,Health, Toxicology and Mutagenesis ,0211 other engineering and technologies ,02 engineering and technology ,010501 environmental sciences ,Pharmacology ,01 natural sciences ,Contractility ,Fluorides ,Mice ,chemistry.chemical_compound ,Protein Interaction Mapping ,Animals ,KEGG ,Potential mechanism ,0105 earth and related environmental sciences ,021110 strategic, defence & security studies ,Public Health, Environmental and Occupational Health ,Proteins ,General Medicine ,Myocardial Contraction ,Pollution ,Rats ,Gene Ontology ,chemistry ,Toxicity ,Cardiomyopathies ,Fluoride ,Biomarkers - Abstract
Fluorosis is a worldwide public health problem, and its adverse effects on the heart have been confirmed by many studies. Abnormal myocardial contractions are often associated with impairment of cardiac function as a cause or consequence. We designed two-part experiments to search for biomarkers and clarify the underlying molecular mechanism of fluoride on myocardial contraction. First, we used Pressure-volume Loop analysis to evaluate changes in myocardial function indexes with multiple fluoride exposure levels in mice (0, 30, 70, and 150 mg/L) exposed for 4 weeks. The results showed that fluoride exposure affects the heart pump function and reduces cardiac contractility. Then, we established a rat model of fluoride exposure (0, 30, 60, and 90 mg/L) for 6 months to carry out proteomic analysis of fluoride-induced myocardial contractile injury. Hematoxylin-eosin (H&E) staining was used to determine the severity of myocardial injury, and myocardial tissue samples were submitted for isobaric tags for relative and absolute quantitation (ITRAQ) analysis. A total of 1607 proteins were successfully identified with 294 differentially expressed proteins (DEPs) in fluoride treated groups. According to Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis, 12 DEPs were confirmed to be involved in pathways related to myocardial contraction. Furthermore, we constructed a protein-protein interaction (PPI) network for these 12 core DEPs to illustrate the role and location of each DEP in the myocardial contraction pathway. The results of this study are helpful for identify a potential mechanism and biomarkers of fluoride-induced myocardial contraction function damage, moreover, which can provide a new insight into the heart toxicity of fluoride in animals at the proteomics level.
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- 2020
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7. Antitumor and immunomodulatory activities of total flavonoids extract from persimmon leaves in H22 liver tumor-bearing mice
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Mengliang Zhang, Xiangyun Gao, Yundong Wei, Jinxia Li, Li Chen, Ying Gao, Xiaoting Yan, Yutong Gao, Shimei Zhao, and Anwen Zhang
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Male ,0301 basic medicine ,Carcinoma, Hepatocellular ,Liver tumor ,Cyclophosphamide ,lcsh:Medicine ,Spleen ,Pharmacology ,Article ,Mice ,03 medical and health sciences ,Antineoplastic Agents, Immunological ,Immune system ,Phagocytosis ,In vivo ,Cell Line, Tumor ,medicine ,Animals ,Humans ,lcsh:Science ,Flavonoids ,Multidisciplinary ,Plant Extracts ,Chemistry ,Macrophages ,Monocyte ,lcsh:R ,Liver Neoplasms ,Diospyros kaki ,Diospyros ,medicine.disease ,Antineoplastic Agents, Phytogenic ,Killer Cells, Natural ,Plant Leaves ,Disease Models, Animal ,030104 developmental biology ,medicine.anatomical_structure ,Cell culture ,lcsh:Q ,Female ,Drug Screening Assays, Antitumor ,medicine.drug - Abstract
Persimmon (Diospyros kaki L.) leaves are commonly used in Asia as tea infusion and as an agent in traditional medicine. The present study aims to explore the antitumor and immunomodulatory effects of total flavonoids extract from persimmon leaves (PLF) in H22 liver tumor-bearing mice. We found that the PLF showed significant inhibition on the liver tumor growth in mice with a tumor inhibition rate of up to 49.35%. In contrast to the severe side effects of cyclophosphamide (CTX), the PLF exhibited anti-cachexia effect and showed no alternation in the body weight and food intake in mice. Moreover, compared with the vehicle control and CTX group, the PLF significantly enhanced the thymus and spleen indices, level of serum interleukin-18 (IL-18), monocyte/macrophage phagocytosis, level of serum hemolysin, and activity of natural killer (NK) cells. This study demonstrated that the PLF could effectively inhibit liver tumor growth in vivo via enhancement of the immune function in mice, and it displayed the potential to be a safe and effective anticancer agent or functional immune-enhancing agent.
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- 2018
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8. Fluoride induces apoptosis and alters collagen I expression in rat osteoblasts
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Xiaoyan Yan, Ji Li, Xiaoting Yan, Qinglin Chen, Alex Morrison, Jundong Wang, and Tianlong Han
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medicine.medical_specialty ,Programmed cell death ,Cell Survival ,Fluorescent Antibody Technique ,Apoptosis ,Protein degradation ,Biology ,Toxicology ,Collagen Type I ,chemistry.chemical_compound ,Internal medicine ,Sodium fluoride ,medicine ,Animals ,Rats, Wistar ,Cells, Cultured ,Messenger RNA ,Osteoblasts ,Reverse Transcriptase Polymerase Chain Reaction ,Cell Cycle ,Osteoblast ,General Medicine ,Cell cycle ,Immunohistochemistry ,Molecular biology ,Rats ,Collagen Type I, alpha 1 Chain ,medicine.anatomical_structure ,Endocrinology ,Animals, Newborn ,chemistry ,Toxicity ,Sodium Fluoride ,Female ,Collagen - Abstract
In this study we investigated apoptosis and expression of the collagen I gene in newborn rat osteoblasts (OB) by the administration of varying concentrations of fluoride (F). Sodium fluoride (NaF) at concentrations of 0, 0.5, 5, 10, and 20mg/L was administered to cultured OB. The percentage of G(1)/G(0) (Gap 1/Gap 0), S (synthesis), G(2)/M (Gap 2/M, mitosis), and apoptosis rates in OB were analyzed with a Fluorescence-activated Cell Sorter (FACS) by propidium iodine (PI) staining after F treatment of 72 h. Effects of F treatment on COL1A1 and COL1A2 mRNA and collagen I protein levels were determined using quantitative real time RT-PCR (qRT-PCR) and immunofluorescence, respectively. This study demonstrates that there is a pronounced negative effect of long term NaF treatment on OB survival. These negative effects include an inhibition of the transformation from S phase into G(2)/M phase, increased apoptosis, and decreased COL1A1 mRNA, down-regulating the synthesis of COL I protein. The results suggest that COL I protein degradation in OB from F toxicity is due to a depletion of COL1A1 mRNA and not COL1A2.
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- 2011
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