28 results on '"Moreira AM"'
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2. Miniaturized systems for gas chromatography: Developments in sample preparation and instrumentation.
- Author
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Crucello J, de Oliveira AM, Sampaio NMFM, and Hantao LW
- Subjects
- Chromatography, Gas methods, Miniaturization methods, Microtechnology, Specimen Handling
- Abstract
An important field of research is the miniaturization of analytical systems for laboratory applications and on-field analysis. In particular, gas chromatography (GC) has benefited from the recent advances in enabling technologies like photolithography, micromachining, hot embossing, and 3D-printing to improve sampling and sample preparation, microcolumn technologies, and detection. In this article, the developments and applications reported since 2015 were reviewed and summarized. Important applications using benchtop instruments, portable GCs, and micro-GCs (µGCs) were showcased to illustrate the current challenges associated with each miniaturized interfaces and systems. For instance, portable instruments need to be energy-efficient and ideally depend on renewable sources for carrier gas generation. Lastly, multidimensional separations were addressed using miniaturized systems to effectively improve the peak capacity of portable systems., Competing Interests: Declaration of Competing Interest The authors have no competing interests to declare that are relevant to the content of this article., (Copyright © 2022 Elsevier B.V. All rights reserved.)
- Published
- 2022
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3. Gut microbiota: A potential therapeutic target for management of diabetic retinopathy?
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Alarcón Yempén RE, Venzel R, Paulino Campos MC, de Oliveira LP, Lins RVD, Pessoni AM, Fanaro GB, de Oliveira Souza A, Calaza KDC, de Brito Alves JL, and Cavalcanti-Neto MP
- Subjects
- Diabetes Mellitus physiopathology, Diabetic Retinopathy therapy, Dysbiosis, Humans, Inflammation physiopathology, Retina metabolism, Diabetic Retinopathy microbiology, Gastrointestinal Microbiome physiology
- Abstract
Diabetic Retinopathy (DR) is one of the main complications of Diabetes Mellitus (DM), drastically impacting individuals of working age over the years, being one of the main causes of blindness in the world. The existing therapies for its treatment consist of measures that aim only to alleviate the existing clinical signs, associated with the microvasculature. These treatments are limited only to the advanced stages and not to the preclinical ones. In response to a treatment with little resolution and limited for many patients with DM, investigations of alternative therapies that make possible the improvement of the glycemic parameters and the quality of life of subjects with DR, become extremely necessary. Recent evidence has shown that deregulation of the microbiota (dysbiosis) can lead to low-grade, local and systemic inflammation, directly impacting the development of DM and its microvascular complications, including DR, in an axis called the intestine-retina. In this regard, the present review seeks to comprehensively describe the biochemical pathways involved in DR as well as the association of the modulation of these mechanisms by the intestinal microbiota, since direct changes in the microbiota can have a drastic impact on various physiological processes. Finally, emphasize the strong potential for modulation of the gut-retina axis, as therapeutic and prophylactic target for the treatment of DR., (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Published
- 2021
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4. Management of Hepatocellular Carcinoma during the COVID-19 Pandemic - São Paulo Clínicas Liver Cancer Group Multidisciplinary Consensus Statement.
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Chagas AL, Fonseca LGD, Coelho FF, Saud LRDC, Abdala E, Andraus W, Fiore L, Moreira AM, Menezes MR, Carnevale FC, Tani CM, Alencar RSSM, D'Albuquerque LAC, Herman P, and Carrilho FJ
- Subjects
- Betacoronavirus, Brazil epidemiology, COVID-19, Consensus, Humans, SARS-CoV-2, Carcinoma, Hepatocellular epidemiology, Carcinoma, Hepatocellular therapy, Coronavirus Infections, Liver Neoplasms epidemiology, Liver Neoplasms therapy, Pandemics, Pneumonia, Viral
- Abstract
More than 18 million people in 188 countries have been diagnosed as having coronavirus disease (COVID-19), and COVID-19 has been responsible for more than 600,000 deaths worldwide. Brazil is now the second most affected country globally. Faced with this scenario, various public health measures and changes in the daily routines of hospitals were implemented to stop the pandemic. Patients with hepatocellular carcinoma (HCC) are at an increased risk for severe COVID-19 as they present with two major diseases: cancer and concomitant chronic liver disease. The COVID-19 pandemic can significantly impact the management of HCC patients from diagnosis to treatment strategies. These patients need special attention and assistance at this time, especially since treatment for tumors cannot be delayed in most cases. The aim of this guideline was to standardize the management of HCC patients during the COVID-19 pandemic. This document was developed, on the basis of the best evidence available, by a multidisciplinary team from Instituto do Câncer do Estado de São Paulo (ICESP), and Instituto Central of the Hospital das Clínicas da Universidade de São Paulo (HC-FMUSP), which are members of the São Paulo Clínicas Liver Cancer Group.
- Published
- 2020
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5. Severe asthma phenotypes in patients controlled with omalizumab: A real-world study.
- Author
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Campo P, Soto Campos G, Aparicio MB, Jorge AM, González Expósito HM, Quirce S, and Dávila I
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- Retrospective Studies, Severity of Illness Index, Treatment Outcome, Asthma drug therapy, Omalizumab therapeutic use, Phenotype
- Abstract
Background: The appropriate identification of asthma phenotypes of responders to omalizumab would optimize the selection of treatment., Objective: To describe the most frequent clinical phenotypes in patients with severe asthma responding to omalizumab and their clinical and pulmonary function improvement., Methods: This was an observational, retrospective, multicenter study. Adult patients with severe asthma, who achieved good control after the first year of treatment with omalizumab were included. Omalizumab was prescribed according to clinical routine practice. Responders were assigned to one pre-established phenotype based on the most predominant one before they had started treatment with omalizumab, all according to the physician's criteria. Data about asthma symptoms, number of non-severe asthma exacerbations, medication intake (inhaled and oral corticosteroids and rescue medication), lung function, high fractional exhaled nitric oxide (FeNO) and peripheral eosinophils counts were recorded., Results: Among the 345 patients included, the main phenotypes were severe asthma with frequent exacerbations (29.9%), early-onset allergic asthma (23.8%), severe steroid-dependent asthma (18.8%), and severe eosinophilic asthma (13.6%). Clinical and respiratory changes observed after first year of treatment with omalizumab included: reduction in asthma symptoms, reduction in the use and dose of corticosteroids and need for rescue therapy, improvement of pulmonary function, reduction in the number of episodes of non-severe asthma exacerbations regardless of the duration of severe disease since the diagnosis. Increased blood levels of peripheral eosinophils and high FeNO levels were found at baseline., Conclusion: Several heterogeneous severe asthma phenotypes were observed as good responders to omalizumab., (Copyright © 2019. Published by Elsevier Ltd.)
- Published
- 2019
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6. Synthetic Mn(III) porphyrins as biomimetic catalysts of CYP450: Degradation of antibiotic norfloxacin in aqueous medium.
- Author
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Meireles AM, Almeida Lage AL, Ribeiro JM, Silva MAND, Souza-Fagundes EM, and Martins DCDS
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- Biomimetics, Catalysis, Hydrogen Peroxide, Oxidation-Reduction, Anti-Bacterial Agents chemistry, Cytochrome P-450 Enzyme System metabolism, Manganese chemistry, Norfloxacin chemistry, Porphyrins analysis, Water Pollutants, Chemical chemistry
- Abstract
Norfloxacin (NOR) is a synthetic broad-spectrum fluoroquinolone antibiotic classified as an emerging contaminant. Here, we investigate Mn(III) porphyrin-catalyzed NOR degradation using peroxides or peracids (H
2 O2 , t-BuOOH, or Oxone®) as oxidants. We evaluate three Mn(III) porphyrins: the 1st -generation tetraphenylporphyrin and 2nd -generation porphyrins bearing halogen atoms at the ortho-positions of the porphyrin macrocycle meso-aryl groups. Experiments were carried out in aqueous medium under mild conditions. NOR degradation was 67%. Products were proposed by mass spectrometry (MS) analysis. Oxone® was the best oxidant for NOR degradation despite its possible decomposition in the reaction medium. The second-generation Mn(III) porphyrins were more resistant than the first-generation Mn(III) porphyrin, indicating that the bulky groups introduced into the porphyrin macrocycle meso-aryl groups led to more robust catalysts. The degradation products did not present cytotoxic behavior under the employed conditions. In conclusion, Mn(III) porphyrin-catalyzed NOR degradation is a promising strategy to degrade fluoroquinolones and other pollutants., (Copyright © 2019 Elsevier Inc. All rights reserved.)- Published
- 2019
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7. Vagus nerve regulates the phagocytic and secretory activity of resident macrophages in the liver.
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Fonseca RC, Bassi GS, Brito CC, Rosa LB, David BA, Araújo AM, Nóbrega N, Diniz AB, Jesus ICG, Barcelos LS, Fontes MAP, Bonaventura D, Kanashiro A, Cunha TM, Guatimosim S, Cardoso VN, Fernandes SOA, Menezes GB, de Lartigue G, and Oliveira AG
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- Animals, Cytokines, Female, Gastrointestinal Tract, Liver pathology, Macrophages immunology, Mice, Mice, Inbred C57BL, Phagocytes metabolism, Sepsis immunology, Vagus Nerve pathology, Vagus Nerve Stimulation methods, Liver immunology, Phagocytosis physiology, Vagus Nerve physiology
- Abstract
The gastrointestinal (GI) tract harbors commensal microorganisms as well as invasive bacteria, toxins and other pathogens and, therefore, plays a pivotal barrier and immunological role against pathogenic agents. The vagus nerve is an important regulator of the GI tract-associated immune system, having profound effects on inflammatory responses. Among GI tract organs, the liver is a key site of immune surveillance, as it has a large population of resident macrophages and receives the blood drained from the guts through the hepatic portal circulation. Although it is widely accepted that the hepatic tissue is a major target for vagus nerve fibers, the role of this neural circuit in liver immune functions is still poorly understood. Herein we used in vivo imaging techniques, including confocal microscopy and scintigraphy, to show that vagus nerve stimulation increases the phagocytosis activity by resident macrophages in the liver, even on the absence of an immune challenge. The activation of this neural circuit in a non-lethal model of sepsis optimized the removal of bacteria in the liver and resulted in the production of anti-inflammatory and pro-regenerative cytokines. Our findings provide new insights into the neural regulation of the immune system in the liver., (Copyright © 2019 Elsevier Inc. All rights reserved.)
- Published
- 2019
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8. Effect of addition of l-carnitine to media for oocyte maturation and embryo culture on development and cryotolerance of bovine embryos produced in vitro.
- Author
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Zolini AM, Carrascal-Triana E, Ruiz de King A, Hansen PJ, Alves Torres CA, and Block J
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- Animals, Cattle, Cryopreservation veterinary, Embryo Culture Techniques methods, Embryo Culture Techniques veterinary, Embryo Transfer veterinary, Female, In Vitro Oocyte Maturation Techniques methods, Pregnancy, Carnitine pharmacology, Culture Media chemistry, Embryonic Development drug effects, In Vitro Oocyte Maturation Techniques veterinary, Oocytes drug effects
- Abstract
The objective of these experiments was to determine the effect of l-carnitine during oocyte maturation or embryo culture on embryo development and cryosurvival. For Experiments 1-3, embryos were produced in vitro using abattoir-derived cumulus-oocyte complexes (COCs). At d 7 after insemination, embryo development was assessed, and blastocyst and expanded blastocyst stage embryos were harvested and subjected to controlled-rate freezing. Post-thaw cryosurvival was determined by re-expansion and hatching rates at 24, 48 and 72 h post-thaw. In Experiment 1, COCs were matured with or without 3.03 mM l-carnitine. There was no effect of l-carnitine supplementation during maturation on embryo development or post-thaw cryosurvival. In experiment 2, presumptive zygotes were cultured in medium supplemented with or without 5% (v/v) fetal bovine serum and l-carnitine at concentrations of 0.0, 0.75, 1.5 and 3.03 mM. There was no effect of l-carnitine treatment on embryo development, but embryos treated with l-carnitine had increased (P ≤ 0.05) post-thaw re-expansion rates, irrespective of concentration. In experiment 3, presumptive zygotes were cultured with or without 0.75 mM l-carnitine from d 1 to d 4, from d 4 to d 7 or for the entire culture period. There was no effect of l-carnitine during culture on embryo development or post-thaw cryosurvival, regardless of the timing of addition. In Experiment 4, COCs were harvested by ovum pick-up from virgin dairy heifers (n = 24) and subjected to in-vitro embryo production with presumptive zygotes cultured with or without 0.75 mM l-carnitine. At d 7 after insemination, morula and blastocyst stage embryos were harvested and subjected to controlled-rate freezing. Lactating Holstein cows (n = 102) were used as recipients and synchronized for timed embryo transfer. At d 7 after anticipated ovulation, a single embryo was thawed and transferred to the ipsilateral uterine horn of each recipient with a corpus luteum. Pregnancy was diagnosed at d 33, 44 and 72 of gestation. l-carnitine had no effect on the percentage of cows pregnant per embryo transfer (P/ET) after transfer of a frozen-thawed embryo. In conclusion, media supplementation with l-carnitine during in vitro embryo production can improve post-thaw cryotolerance as assessed in vitro but had no effect on P/ET after transfer of frozen-thawed embryos., (Copyright © 2019 Elsevier Inc. All rights reserved.)
- Published
- 2019
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9. Immune and metabolic shifts during neonatal development reprogram liver identity and function.
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Nakagaki BN, Mafra K, de Carvalho É, Lopes ME, Carvalho-Gontijo R, de Castro-Oliveira HM, Campolina-Silva GH, de Miranda CDM, Antunes MM, Silva ACC, Diniz AB, Alvarenga DM, Lopes MAF, de Souza Lacerda VA, Mattos MS, Araújo AM, Vidigal PVT, Lima CX, Mahecha GAB, Madeira MFM, Fernandes GR, Nogueira RF, Moreira TG, David BA, Rezende RM, and Menezes GB
- Subjects
- Adult, Animals, Animals, Newborn, Biopsy, Escherichia coli Infections immunology, Female, Hepatocytes, Humans, Lipid Metabolism, Liver cytology, Metabolome, Mice, Mice, Inbred C57BL, Myeloid Progenitor Cells immunology, Myeloid Progenitor Cells physiology, Nutritive Value physiology, Phagocytes immunology, Precursor Cells, B-Lymphoid immunology, Weaning, Infant, Newborn, Liver immunology, Liver metabolism
- Abstract
Background & Aims: The liver is the main hematopoietic site in embryos, becoming a crucial organ in both immunity and metabolism in adults. However, how the liver adapts both the immune system and enzymatic profile to challenges in the postnatal period remains elusive. We aimed to identify the mechanisms underlying this adaptation., Methods: We analyzed liver samples from mice on day 0 after birth until adulthood. Human biopsies from newborns and adults were also examined. Liver immune cells were phenotyped using mass cytometry (CyTOF) and expression of several genes belonging to immune and metabolic pathways were measured. Mortality rate, bacteremia and hepatic bacterial retention after E. coli challenge were analyzed using intravital and in vitro approaches. In a set of experiments, mice were prematurely weaned and the impact on gene expression of metabolic pathways was evaluated., Results: Human and mouse newborns have a sharply different hepatic cellular composition and arrangement compared to adults. We also found that myeloid cells and immature B cells primarily compose the neonatal hepatic immune system. Although neonatal mice were more susceptible to infections, a rapid evolution to an efficient immune response was observed. Concomitantly, newborns displayed a reduction of several macronutrient metabolic functions and the normal expression level of enzymes belonging to lipid and carbohydrate metabolism was reached around the weaning period. Interestingly, early weaning profoundly disturbed the expression of several hepatic metabolic pathways, providing novel insights into how dietary schemes affect the metabolic maturation of the liver., Conclusion: In newborns, the immune and metabolic profiles of the liver are dramatically different to those of the adult liver, which can be explained by the differences in the liver cell repertoire and phenotype. Also, dietary and antigen cues may be crucial to guide liver development during the postnatal phase., Lay Summary: Newborns face major challenges in the extra-uterine life. In fact, organs need to modify their cellular composition and gene expression profile in order to adapt to changes in both microbiota and diet throughout life. The liver is interposed between the gastrointestinal system and the systemic circulation, being the destination of all macronutrients and microbial products from the gut. Therefore, it is expected that delicately balanced mechanisms govern the transformation of a neonatal liver to a key organ in adults., (Copyright © 2018 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.)
- Published
- 2018
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10. Long-term outcomes of transmesenteric portal vein recanalization for the treatment of chronic portal vein thrombosis after pediatric liver transplantation.
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Cavalcante ACBS, Zurstrassen CE, Carnevale FC, Pugliese RPS, Fonseca EA, Moreira AM, Matushita JPK Jr, Cândido HLL, Benavides MAR, Miura IK, Danesi VLB, Hirschfeld APM, Borges CBV, Porta G, ChapChap P, and Seda-Neto J
- Subjects
- Child, Child, Preschool, Female, Follow-Up Studies, Graft Rejection etiology, Graft Survival, Humans, Infant, Male, Portal Vein pathology, Prognosis, Retrospective Studies, Risk Factors, Survival Rate, Venous Thrombosis etiology, Graft Rejection prevention & control, Liver Diseases surgery, Liver Regeneration, Liver Transplantation adverse effects, Portal Vein surgery, Venous Thrombosis surgery
- Abstract
Portal vein thrombosis (PVT) may occur at any time following liver transplantation. We describe our experience with portal vein recanalization in cases of thrombosis after liver transplantation. Twenty-eight children (5%) out of 566 liver transplant recipients underwent portal vein recanalization using a transmesenteric approach. All children received left hepatic segments, developed PVT, and had symptoms or signs of portal hypertension. Portal vein recanalization was performed via the transmesenteric route in all cases. Twenty-two (78.6%) patients underwent successful recanalization and stent placement. They received oral anticoagulants after the procedure, and clinical symptoms subsided. Symptoms recurred due to portal vein restenosis/thrombosis in seven patients. On an intention-to-treat basis, the success rate of the proposed treatment was 60.7%. Only 17 out of 28 children with posttransplant chronic PVT retained stent patency (primary + assisted) at the end of the study period. In cases of portal vein obstruction, the transmesenteric approach via minilaparotomy is technically feasible with good clinical and hemodynamic results. It is an alternative procedure to reestablish the portal flow to the liver graft that can be performed in selected cases and a therapeutic addition to other treatment strategies currently used to treat chronic PVT., (© 2018 The American Society of Transplantation and the American Society of Transplant Surgeons.)
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- 2018
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11. Relationships between soil organic matter pools and nitrous oxide emissions of agroecosystems in the Brazilian Cerrado.
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de Figueiredo CC, de Oliveira AD, Dos Santos IL, Ferreira EAB, Malaquias JV, de Sá MAC, de Carvalho AM, and Dos Santos JDG Jr
- Abstract
In the Brazilian Cerrado, despite the increasing adoption of no-till systems, there are still extended areas under conventional soil management systems that reduce soil carbon (C) and nitrogen (N) stocks and increase the emissions of greenhouse gases, such as nitrous oxide (N
2 O). Conservation agroecosystems, such as no-till, have been proposed as a strategy to mitigate agriculture-induced climatic changes through reductions in N2 O emissions. However, the relationship between organic matter and N2 O emissions from soils under different agroecosystems is not yet clear. This study hypothesized that agroecosystems under no-till promote an accumulation of labile and stable SOM fractions along with a reduction of N2 O emissions. This study evaluated the effects of crop-rotation agroecosystems: i) on C and N pools and labile and stable SOM fractions; ii) on cumulative N2 O emissions; and iii) on the relationships between SOM fractions and N2 O emissions. The agricultural systems consisted of: (I) soybean followed by sorghum under no-tillage (NT1); (II) maize followed by pigeon pea under no-tillage (NT2); (III) soybean under conventional tillage followed by fallow soil (CT); (IV) and native Cerrado (CER). After CT for 18years, following the replacement of CER, the soil C stock in the 0-20cm layer was reduced by 0.64tha-1 year-1 . The no-till systems were more efficient in accumulating labile and stable C fractions with values close to those observed under CER, and were directly related to lower soil N2 O emissions. The cumulative pattern of N2 O emissions was inverse to that of the following SOM fractions: microbial biomass carbon, permanganate-oxidizable carbon, particulate organic carbon, inert carbon, and humic substances. Based on principal component analysis, the CT was generally separated from the other land use systems. This separation was strongly influenced by the low C contents in the different SOM fractions and higher N2 O emissions promoted by the CT., (Copyright © 2017 Elsevier B.V. All rights reserved.)- Published
- 2018
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12. Distribution pattern of anthropogenic marine debris along the gastrointestinal tract of green turtles (Chelonia mydas) as implications for rehabilitation.
- Author
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Colferai AS, Silva-Filho RP, Martins AM, and Bugoni L
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- Animals, Brazil, Water Pollutants analysis, Gastrointestinal Tract, Plastics, Turtles
- Abstract
Pollution from anthropogenic marine debris (AMD) is currently the most widely distributed and lasting anthropic impact in the marine environment, affecting hundreds of species, including all sea turtles. In this study, the patterns of AMD distribution along the gastrointestinal tract (GT) and their relationship with obstructions and faecalomas in 62 green turtles (Chelonia mydas) that died during rehabilitation in southern Brazil were determined. The GT was split in seven sections, corresponding to the natural organs and intestinal areas morphologically and physiologically distinct. Mean mass (4.24g) and area (146.74cm
2 ) of AMD in the stomach were higher than in other sections. The anterior portion of the rectum had the highest number of obstructions, followed by the stomach. AMD was associated with the obstructions, with positive correlation between faecalomas and AMD masses. Organs and subdivisions showed marked differences in susceptibility to obstructions caused by AMD, which deserves attention in clinical interventions., (Copyright © 2017 Elsevier Ltd. All rights reserved.)- Published
- 2017
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13. Desomorphine (Krokodil): An overview of its chemistry, pharmacology, metabolism, toxicology and analysis.
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Florez DHÂ, Dos Santos Moreira AM, da Silva PR, Brandão R, Borges MMC, de Santana FJM, and Borges KB
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- Analgesics, Opioid adverse effects, Analgesics, Opioid pharmacokinetics, Analgesics, Opioid toxicity, Behavior, Addictive, Codeine adverse effects, Codeine pharmacokinetics, Codeine pharmacology, Codeine toxicity, Humans, Illicit Drugs adverse effects, Illicit Drugs pharmacokinetics, Illicit Drugs toxicity, Infections chemically induced, Analgesics, Opioid pharmacology, Codeine analogs & derivatives, Illicit Drugs pharmacology, Opioid-Related Disorders
- Abstract
Background: "Krokodil" or "Crocodile" is an illegal homemade desomorphine drug obtained from chemical reactions of commercial codeine drugs with several other powerful and highly toxic chemical agents increasing its addiction and hallucinogenic effects when compared with other morphine analogues., Methods: This paper summarizes a complete review about an old drug called desomorphine (Krokodil), presenting its chemistry, pharmacology, metabolism, toxicology and analysis., Results: It is of particular interest and concern because this cheaper injectable semisynthetic opioid drug has been largely used in recent years for recreational purposes in several Eastern European as well as North and South American countries, despite known damage to health that continuous use might induce. These injuries are much stronger and more aggressive than morphine's, infecting and rotting skin and soft tissue to the bone of addicts at the point of injection in less than three years, which, in most cases, evolves to death. On this basis, it is imperative that literature reviews focus on the chemistry, pharmacology, toxicology and analysis of dangerous Krokodil to find strategies for rapid and effective determination to mitigate its adverse effects on addicts and prevent consumption., Conclusions: It is crucial to know the symptoms and consequences of the use of Krokodil, as well as METHODS: for identification and quantification of desomorphine, contaminants and metabolites, which can help the forensic work of diagnosis and propose actions to control and eradicate this great danger to public health around the world., (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Published
- 2017
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14. Clinical and laboratory profile of patients with sickle cell anemia.
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Sant'Ana PG, Araujo AM, Pimenta CT, Bezerra ML, Junior SP, Neto VM, Dias JS, Lopes AF, Rios DR, and Pinheiro MB
- Abstract
Objective: This study aimed to describe and analyze clinical and laboratory characteristics of patients with sickle cell anemia treated at the Hemominas Foundation, in Divinópolis, Brazil. Furthermore, this study aimed to compare the clinical and laboratory outcomes of the group of patients treated with hydroxyurea with those patients that were not treated with hydroxyurea., Methods: Clinical and laboratorial data were obtained by analyzing medical records of patients with sickle cell anemia., Results: Data from the medical records of 50 patients were analyzed. Most of the patients were female (56%), aged between 20 and 29 years old. Infections, transfusions, cholecystectomy, splenectomy and systemic arterial hypertension were the most common clinical adverse events of the patients. The most frequent cause of hospitalization was painful crisis. The majority of patients had reduced values of hemoglobin and hematocrit (8.55±1.33g/dL and 25.7±4.4%, respectively) and increased fetal hemoglobin levels (12±7%). None of the clinical variables was statistically significant on comparing the two groups of patients. Among hematological variables only hemoglobin and hematocrit levels were statistically different between patients treated with hydroxyurea and untreated patients (p-value=0.005 and p-value=0.001, respectively)., Conclusion: Sickle cell anemia requires treatment and follow-up by a multiprofessional team. A current therapeutic option is hydroxyurea. This drug reduces complications and improves laboratorial parameters of patients. In this study, the use of the drug increased the hemoglobin and hematocrit levels of patients., (Copyright © 2016 Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular. Published by Elsevier Editora Ltda. All rights reserved.)
- Published
- 2017
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15. Connexin 37 and 43 gene and protein expression and developmental competence of isolated ovine secondary follicles cultured in vitro after vitrification of ovarian tissue.
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Sampaio da Silva AM, Bruno JB, de Lima LF, Ribeiro de Sá NA, Lunardi FO, Ferreira AC, Vieira Correia HH, de Aguiar FL, Araújo VR, Lobo CH, de Alencar Araripe Moura A, Campello CC, Smitz J, de Figueiredo JR, and Ribeiro Rodrigues AP
- Subjects
- Animals, Apoptosis, Cell Culture Techniques veterinary, Cell Proliferation, Connexin 43 genetics, Connexins genetics, Cryopreservation veterinary, Female, Fluorescent Antibody Technique, Gene Expression, Gene Expression Regulation, Developmental, Ovarian Follicle cytology, Ovarian Follicle metabolism, RNA, Messenger metabolism, Vitrification, Gap Junction alpha-4 Protein, Connexin 43 metabolism, Connexins metabolism, Ovarian Follicle growth & development, Sheep
- Abstract
Cryoinjuries caused by vitrification of tissues and organs lead to the loss of membrane proteins that mediate intercellular communications, such as connexins 37 (Cx37) and 43 (Cx43). Thus, the present study aimed to evaluate ovine Cx37 and Cx43 gene and protein expressions and developmental competence by in vitro-cultured secondary follicles retrieved from vitrified ovarian tissue. Ovarian fragments for the same ovary pair were distributed into six treatments: (1) fresh ovarian tissue (FOT); (2) vitrified ovarian tissue (VOT); (3) isolated follicles from fresh ovarian tissue (FIF); (4) isolated follicles from vitrified ovarian tissue; (5) isolated follicles from fresh ovarian tissue followed by in vitro culture (CFIF); (6) isolated follicles from vitrified ovarian tissue followed by in vitro culture (CVIF). In all treatments, Cx37 and Cx43 gene and protein expression patterns were evaluated by reverse transcription polymerase chain reaction and immunocytochemistry. In addition, secondary follicles were analyzed according to follicular integrity and growth, apoptosis, and cell proliferation. In vitro-cultured secondary follicles (CFIF and CVIF) were evaluated based on morphology (extruded follicles), antrum formation, and viability. The percentage of intact follicles was higher, whereas antrum formation, oocyte extrusion rate, and follicle viability were lower in CVIF than in CFIF treatment (P < 0.05). Terminal deoxynucleotidyl transferase-mediated biotinylated deoxyuridine triphosphates nick end-labeling assay demonstrated that apoptosis was absent in FIF, whereas follicles from all other treatments showed positive labeling. Cell proliferation index was higher in isolated follicles from vitrified ovarian tissue and CVIF treatments than in follicles from FIF. Expression of Cx43 messenger RNA was lower in CVIF treatment when compared with follicles from all other treatments (P < 0.05). Follicle Cx37 messenger RNA levels did not show alterations in any treatment (P > 0.05). Cx37 and Cx43 immunolabeling was localized mainly on granulosa cells and oocytes, respectively. In conclusion, isolation of ovine secondary follicles could be done successfully after vitrification of ovarian tissue, and the basement membrane integrity remained intact after in vitro culture. Although the gene and protein expression of Cx37 did not change after vitrification of ovarian tissue, Cx43 turned out to be altered in secondary follicles after vitrification and in vitro culture., (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Published
- 2016
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16. Oral health-related quality of life of children and teens with sickle cell disease.
- Author
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da Matta Felisberto Fernandes ML, Kawachi I, Fernandes AM, Corrêa-Faria P, Paiva SM, and Pordeus IA
- Abstract
Background: Children with sickle cell disease may have their quality of life affected by oral alterations. However, there is still little data on oral health-related quality of life in these children. The aim of this study was to investigate the influence of sickle cell disease, socioeconomic characteristics, and oral conditions on oral health-related quality of life of children and teens., Method: One hundred and six children and teens with sickle cell disease were compared to a similar sample of 385 healthy peers. Data were collected through oral examinations, interviews to assess quality of life (Child Perceptions Questionnaire for children aged 8-10 and 11-14) and questionnaires containing questions on socioeconomic status., Results: There were no statistically significant differences in the total scores of the Child Perceptions Questionnaires or domain scores comparing sickle cell disease patients to control subjects. When sub-scales were compared, oral symptoms and functional limitations had a greater negative impact on the quality of life of adolescents with sickle cell disease (p-value <0.001 and p-value <0.01, respectively) when compared to healthy controls. The only statistically significant determinants of negative impact on oral health-related quality of life in the overall sample was home overcrowding (more than two people/room) in the younger children's group, and dental malocclusion among teens., Conclusion: There was no significant difference in the negative impact on the oral health-related quality of life between the group with sickle cell disease and the control group. Of the oral alterations, there was a significant difference in the oral health-related quality of life between adolescents with sickle cell disease and controls only in relation to malocclusion. Among the socioeconomic characteristics, only overcrowding was significantly associated with a negative impact on oral health-related quality of life., (Copyright © 2016 Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular. Published by Elsevier Editora Ltda. All rights reserved.)
- Published
- 2016
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17. On the study of the role of NO-mediated pathways in the myocardial response to acute stretch.
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Leite-Moreira AM, Neves JS, Almeida-Coelho J, Neiva-Sousa M, and Leite-Moreira AF
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- Humans, Myocardial Contraction, Myocytes, Cardiac metabolism, Nitric Oxide metabolism
- Published
- 2016
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18. Prognostic value of KRAS mutations in stage III colon cancer: post hoc analysis of the PETACC8 phase III trial dataset.
- Author
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Thaler J, Greil R, Gaenzer J, Eisterer W, Tschmelitsch J, Samonigg H, Zabernigg A, Schmid F, Steger G, Steinacher R, Andel J, Lang A, Függer R, Hofbauer F, Woell E, Geissler D, Lenauer A, Prager M, Van Laethem JL, Van Cutsem E, D'Haens G, Demolin G, Kerger J, Deboever G, Ghillebert G, Polus M, Van Cutsem E, RezaieKalantari H, Delaunoit T, Goeminne JC, Peeters M, Vergauwe P, Houbiers G, Humblet Y, Janssens J, Schrijvers D, Vanderstraeten E, Van Laethem JL, Vermorken J, Van Daele D, Ferrante M, Forget F, Hendlisz A, Yilmaz M, Nielsen SE, Vestermark L, Larsen J, Ychou M, Zawadi A, Zawadi MA, Bouche O, Mineur L, Bennouna-Louridi J, Dourthe LM, Ychou M, Boucher E, Taieb J, Pezet D, Desseigne F, Ducreux M, Texereau P, Miglianico L, Rougier P, Fratte S, Levache CB, Merrouche Y, Ellis S, Locher C, Ramee JF, Garnier C, Viret F, Chauffert B, Cojean-Zelek I, Michel P, Lecaille C, Borel C, Seitz JF, Smith D, Lombard-Bohas C, Andre T, Gornet JM, Fein F, Coulon-Sfairi MA, Kaminsky MC, Lagasse JP, Luet D, Etienne PL, Gasmi M, Vanoli A, Nguyen S, Aparicio T, Perrier H, Stremsdoerfer N, Laplaige P, Arsene D, Auby D, Bedenne L, Coriat R, Denis B, Geoffroy P, Piot G, Becouarn Y, Bordes G, Deplanque G, Dupuis O, Fruge F, Guimbaud R, Lecomte T, Lledo G, Sobhani I, Asnacios A, Azzedine A, Desauw C, Galais MP, Gargot D, Lam YH, Abakar-Mahamat A, Berdah JF, Catteau S, Clavero-Fabri MC, Codoul JF, Legoux JL, Goldfain D, Guichard P, Verge DP, Provencal J, Vedrenne B, Brezault-Bonnet C, Cleau D, Desir JP, Fallik D, Garcia B, Gaspard MH, Genet D, Hartwig J, Krummel Y, MatysiakBudnik T, Palascak-Juif V, Randrianarivelo H, Rinaldi Y, Aleba A, Darut-Jouve A, de Gramont A, Hamon H, Wendehenne F, Matzdorff A, Stahl MK, Schepp W, Burk M, Mueller L, Folprecht G, Geissler M, Mantovani-Loeffler L, Hoehler T, Asperger W, Kroening H, von Weikersthal LF, Fuxius S, Groschek M, Meiler J, Trarbach T, Rauh J, Ziegenhagen N, Kretzschmar A, Graeven U, Nusch A, von Wichert G, Hofheinz RD, Kleber G, Schmidt KH, Vehling-Kaiser U, Baum C, Schuette J, Haag GM, Holtkamp W, Potenberg J, Reiber T, Schliesser G, Schmoll HJ, Schneider-Kappus W, Abenhardt W, Denzlinger C, Henning J, Marxsen B, GuenterDerigs H, Lambertz H, Becker-Boost I, Caca K, Constantin C, Decker T, Eschenburg H, Gabius S, Hebart H, Hoffmeister A, Horst HA, Kremers S, Leithaeuser M, Mueller S, Wagner S, Daum S, Schlegel F, Stauch M, Heinemann V, Labianca R, Colucci G, Amadori D, Mini E, Falcone A, Boni C, Maiello E, Latini L, Zaniboni A, Amadori D, Aprile G, Barni S, Mattioli R, Martoni A, Passalacqua R, Nicolini M, Pasquini E, Rabbi C, Aitini E, Ravaioli A, Barone C, Biasco G, Tamberi S, Gambi A, Verusio C, Marzola M, Lelli G, Boni C, Cascinu S, Bidoli P, Vaghi M, Cruciani G, Di Costanzo F, Sobrero A, Mini E, Petrioli R, Aglietta M, Alabiso O, Capuzzo F, Falcone A, Corsi DC, Labianca R, Salvagni S, Chiara S, Ferraù F, Giuliani F, Lonardi S, Gebbia N, Mantovani G, Sanches E, Sanches E, Mellidez JC, Santos P, Freire J, Sarmento C, Costa L, Pinto AM, Barroso S, Santo JE, Guedes F, Monteiro A, Sa A, Furtado I, Tabernero J, Salazar R, Aguilar EA, Herrero FR, Tabernero J, Valera JS, ValladaresAyerbes M, FeliuBatlle J, Gil S, Garcia-Giron C, Vivanco GL, Salvia AS, Orduña VA, Garcia RV, Gallego J, Sureda BM, Remon J, Safont Aguilera MJ, CireraNogueras L, Merino B, Castro CG, de Prado PM, PijaumePericay C, ConstenlaFigueiras M, Jordan I, GomeReina MJ, Garcia AL, Garcia-Ramos AA, Cervantes A, Martos CF, MarcuelloGaspar E, Montero IC, Emperador PE, Carbonero AL, Castillo MG, Garcia TG, Lopez JG, Flores EG, GuillotMorales M, LlanosMuñoz M, Martín AL, Maurel J, Camara JC, Garcia RD, Salgado M, HernandezBusquier I, Ruiz TC, LacastaMuñoa A, Aliguer M, Ortiz de Taranco AV, Ureña MM, Gaspa FL, Ponce JJ, Roig CB, Jimenez PV, GalanBrotons A, AlbiolRodriguez S, Martinez JA, Ruiz LC, CentellesRuiz M, Bridgewater J, Glynne-Jones R, Tahir S, Hickish T, Cassidy J, and Samuel L
- Published
- 2015
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19. Effects of two lipid lowering therapies on immune responses in hyperlipidemic subjects.
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Moreira FT, Ramos SC, Monteiro AM, Helfenstein T, Gidlund M, Damasceno NR, Neto AM, Izar MC, and Fonseca FA
- Subjects
- Antibodies blood, Azetidines pharmacology, Cholesterol, LDL blood, Ezetimibe, Fluorobenzenes pharmacology, HLA-D Antigens immunology, Humans, Hypolipidemic Agents pharmacology, Immune System drug effects, Pyrimidines pharmacology, Rosuvastatin Calcium, Sulfonamides pharmacology, Antibodies metabolism, Azetidines therapeutic use, Fluorobenzenes therapeutic use, Hyperlipidemias drug therapy, Hyperlipidemias immunology, Hypolipidemic Agents therapeutic use, Pyrimidines therapeutic use, Sulfonamides therapeutic use
- Abstract
Aims: To compare the effects of two of the most effective lipid-lowering therapies with similar LDL-cholesterol reduction capacity on the innate and adaptive immune responses through the evaluation of autoantibodies anti-oxidized LDL (anti-oxLDL Abs) and electronegative LDL [LDL(-)] levels., Main Methods: We performed a prospective, randomized, open label study, with parallel arms and blinded endpoints. One hundred and twelve subjects completed the study protocol and received rosuvastatin 40 mg or ezetimibe/simvastatin 10/40 mg for 12 weeks. Lipids, apolipoproteins, LDL(-), and anti-oxLDL Abs (IgG) were assayed at baseline and end of study., Key Findings: Main clinical and laboratory characteristics were comparable at baseline. Lipid modifications were similar in both treatment arms, however, a significant raise in anti-oxLDL Abs levels was observed in subjects treated with rosuvastatin (p=0.026 vs. baseline), but not in those receiving simvastatin/ezetimibe. (p=0.233 vs. baseline), thus suggesting modulation of adaptive immunity by a potent statin. Titers of LDL(-) were not modified by the treatments., Significance: Considering atherosclerosis as an immune disease, this study adds new information, showing that under similar LDL-cholesterol reduction, the choice of lipid-lowering therapy can differently modulate adaptive immune responses., (Copyright © 2014 Elsevier Inc. All rights reserved.)
- Published
- 2014
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20. Association of autoantibodies anti-OxLDL and markers of inflammation with stage of HIV infection.
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Orellana RV, Fonseca HA, Monteiro AM, Ortega KL, Gallottini MH, Gidlund M, and Pobocik AM
- Subjects
- Adult, Biomarkers blood, Cross-Sectional Studies, Female, Humans, Inflammation blood, Inflammation diagnosis, Male, Middle Aged, Autoantibodies blood, HIV Infections blood, HIV Infections diagnosis, Lipoproteins, LDL blood
- Published
- 2013
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21. Inflammatory environment and immune responses to oxidized LDL are linked to systolic and diastolic blood pressure levels in hypertensive subjects.
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da Fonseca HA, Fonseca FA, Monteiro AM, Farias NC Jr, Bianco HT, Brandão SA, Póvoa RM, Gidlund M, and Izar MC
- Subjects
- Aged, Female, Humans, Hypertension metabolism, Hypertension pathology, Inflammation immunology, Inflammation metabolism, Male, Middle Aged, Adaptive Immunity, Blood Pressure immunology, Hypertension immunology, Lipoproteins, LDL metabolism
- Published
- 2012
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22. Concomitant prescribing and dispensing errors at a Brazilian hospital: a descriptive study.
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Silva Md, Rosa MB, Franklin BD, Reis AM, Anchieta LM, and Mota JA
- Subjects
- Brazil, Child, Cross-Sectional Studies, Humans, Inappropriate Prescribing prevention & control, Medication Systems, Hospital statistics & numerical data, Pharmacy Service, Hospital statistics & numerical data, Drug Prescriptions statistics & numerical data, Hospitals, Pediatric statistics & numerical data, Inappropriate Prescribing statistics & numerical data, Pharmaceutical Preparations administration & dosage
- Abstract
Objective: To analyze the prevalence and types of prescribing and dispensing errors occurring with high-alert medications and to propose preventive measures to avoid errors with these medications., Introduction: The prevalence of adverse events in health care has increased, and medication errors are probably the most common cause of these events. Pediatric patients are known to be a high-risk group and are an important target in medication error prevention., Methods: Observers collected data on prescribing and dispensing errors occurring with high-alert medications for pediatric inpatients in a university hospital. In addition to classifying the types of error that occurred, we identified cases of concomitant prescribing and dispensing errors., Results: One or more prescribing errors, totaling 1,632 errors, were found in 632 (89.6%) of the 705 high-alert medications that were prescribed and dispensed. We also identified at least one dispensing error in each high-alert medication dispensed, totaling 1,707 errors. Among these dispensing errors, 723 (42.4%) content errors occurred concomitantly with the prescribing errors. A subset of dispensing errors may have occurred because of poor prescription quality. The observed concomitancy should be examined carefully because improvements in the prescribing process could potentially prevent these problems., Conclusion: The system of drug prescribing and dispensing at the hospital investigated in this study should be improved by incorporating the best practices of medication safety and preventing medication errors. High-alert medications may be used as triggers for improving the safety of the drug-utilization system.
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- 2011
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23. Prevalence of potential drug interactions in patients in an intensive care unit of a university hospital in Brazil.
- Author
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Reis AM and Cassiani SH
- Subjects
- Adult, Aged, Brazil, Cross-Sectional Studies, Drug Interactions, Female, Hospitalization, Humans, Intensive Care Units statistics & numerical data, Male, Middle Aged, Pharmacoepidemiology, Retrospective Studies, Risk Factors, Statistics, Nonparametric, Time Factors, Drug Monitoring statistics & numerical data, Drug-Related Side Effects and Adverse Reactions
- Abstract
Objectives: To investigate the prevalence of potential drug interactions at the intensive care unit of a university hospital in Brazil and to analyze their clinical significance., Methods: This cross-sectional retrospective study included 299 patients who had been hospitalized in the intensive care unit of the hospital. The drugs administered during the first 24 hours of hospitalization, in the 50th length-ofstay percentile and at the time of discharge were analyzed to identify potential drug-drug and drug-enteral nutrition interactions using DRUG-REAXH software. The drugs were classified according to the anatomical therapeutic chemical classification., Results: The median number of medications per patient was smaller at the time of discharge than in the 50th length-of-stay percentile and in the first 24 hours of hospitalization. There was a 70% prevalence of potential drug interactions at the intensive care unit at the studied time points of hospitalization. Most of the drug interactions were either severe or moderate, and the scientific evidence for the interactions was, in general, either good or excellent. Pharmacodynamic interactions presented a subtle predominance in relation to pharmacokinetic interactions. The occurrence of potential drug interactions was associated with the number of medications administered and the length of stay. Medications that induced cytochrome P450, drugs that prolong the QT interval and cardiovascular drugs were pharmacotherapy factors associated with potential drug interactions., Conclusion: The study showed that potential drug interactions were prevalent in the intensive care unit due to the complexity of the pharmacotherapies administered. The interactions were associated with the number of drugs, the length of stay and the characteristics of the administered medications.
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- 2011
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24. Acquired Pelger-Huët: what does it really mean?
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Dusse LM, Moreira AM, Vieira LM, Rios DR, Silva RM, and Carvalho Md
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- Diagnosis, Differential, Humans, Hematologic Diseases pathology, Neutrophils pathology, Pelger-Huet Anomaly pathology
- Abstract
Pelger-Huët anomaly (PHA) is a benign inherited condition characterized by hyposegmentation of the neutrophil's nucleus and excessive chromatin clumping. An acquired neutrophil dysplasia similar to PHA has been described in hematological diseases and in some clinical conditions. It has been known as acquired or pseudo PHA. Although some hypotheses have been proposed to explain this phenomenon, the mechanism of nuclear change is still unclear. Only the laboratory and clinical data combined will yield a better understanding on the need for follow-up and management of patients in the appropriate cases. In addition, a possible cause of pseudo PHA must always be investigated to add insights to the full understanding of this abnormality. Whether this neutrophil phenomenon has clinical implications remains to be elucidated. It is clear that only a small number of patients under drugs (immunosuppressive and others) may present these neutrophil abnormalities. Most of them do not show this phenomenon and we are unable to explain the different responses in drug users. Whether these patients display a predisposition for developing bone marrow or other diseases in the future, it is a very intriguing matter and only a follow-up will solve this question., (2010 Elsevier B.V. All rights reserved.)
- Published
- 2010
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25. Enhancement on the Europium emission band of Europium chlortetracycline complex in the presence of LDL.
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Teixeira Ldos S, Grasso AN, Monteiro AM, Neto AM, Vieira ND Jr, Gidlund M, and Courrol LC
- Subjects
- Biosensing Techniques, Humans, Time Factors, Chlortetracycline chemistry, Cholesterol, LDL analysis, Europium chemistry, Spectrophotometry methods
- Abstract
Low-density lipoprotein (LDL) particles are the major cholesterol-carrying lipoprotein in the human circulation from the liver to peripheral tissues. High levels of LDL-Cholesterol (LDL-C) are known risk factor for the development of coronary artery disease (CAD). The most common approach to determine the LDL-C in the clinical laboratory involves the Friedewald formula. However, in certain situations, this approach is inadequate. In this paper we report on the enhancement on the Europium emission band of Europium chlortetracycline complex (CTEu) in the presence of LDL. The emission intensity at 615 nm of the CTEu increases with increasing amounts of LDL. This phenomenon allowed us to propose a method to determine the LDL concentration in a sample composed by an aqueous solution of LDL. With this result we obtained LDL calibration curve, LOD (limit of detection) of 0.49 mg/mL and SD (standard deviation) of 0.003. We observed that CTEu complex provides a wider dynamic concentration-range for LDL determination than that from Eu-tetracycline previously. The averaged emission lifetimes of the CTEu and CTEu with LDL (1.5 mg/mL) complexes were measured as 15 and 46 micros, respectively. Study with some metallic interferents is presented., (2010 Elsevier Inc. All rights reserved.)
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- 2010
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26. Acquired Pelger-Huët anomaly associated with ibuprofen therapy.
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Moreira AM, Vieira LM, Rios DR, Carvalho Md, and Dusse LM
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- Child, Chromatin metabolism, Female, Humans, Neutrophils pathology, Pelger-Huet Anomaly blood, Ibuprofen adverse effects, Pelger-Huet Anomaly chemically induced, Pelger-Huet Anomaly etiology
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- 2009
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27. Inclusion of carvone enantiomers in cyclomaltoheptaose (beta-cyclodextrin): thermal behaviour and H-->D and D-->H exchange.
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da Silva AM, Empis JM, and Teixeira-Dias JJ
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- Binding Sites, Cyclohexane Monoterpenes, Deuterium, Hydrogen, Monoterpenes, Spectrum Analysis, Raman, Stereoisomerism, Temperature, Water chemistry, Cyclodextrins chemistry, Terpenes chemistry, beta-Cyclodextrins
- Abstract
The inclusion compounds of carvone enantiomers in cylcomaltoheptaose (beta-cyclodextrin, betaCD) are studied at defined temperatures above room temperature and in relation to H-->D and D-->H exchanges. Loss of water molecules and release of carvone molecules from the betaCD cavity are caused by increase of temperature above room temperature and are measured by the integrated intensities of the O-H and C-H Raman stretching bands, respectively. In turn, H-->D and D-->H exchanges are monitored by the integrated intensities of the O-H and O-D Raman stretching bands, respectively. All of these processes were followed in real time with a Raman spectrometer equipped with CCD detection. The results indicate that distinct carvone enantiomers lead to the formation of different betaCD inclusion hydrates that have different water content and hydration structures. In particular, the results suggest that SCarv-betaCD has a greater water content, dehydrates strongly for temperatures above room temperature, and exchanges protons faster than the RCarv-betaCD complex.
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- 2002
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28. Occurrence and Characterization of Aeromonas Species in Pasteurized Milk and White Cheese in Rio De Janeiro, Brazil.
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Freitas AC, Nunes MP, Milhomem AM, and Ricciardi ID
- Abstract
A total of 35 samples (1000 ml each) of pasteurized milk and 25 samples (100 g each) of white cheese purchased at supermarkets in Rio de Janeiro were analyzed for the presence of Aeromonas . Strains of Aeromonas were isolated from 28.5% of pasteurized milk and 32% of white cheese samples. Standard Plate counts in the pasteurized milk samples ranged from 7.2 × 10
* to 2.5 × 105 CFU/ml. Total and fecal coliform counts in white cheese samples ranged from 1.9 × 10* to 2.4 × 105 most probable number per g and 3.2 × 102 to 1.2 × 105 most probable number per g, respectively. It was possible to identify Aeromonas caviae (58.9%), Aeromonas hydrophila (12.8%), and Aeromonas schubertii (2.5%) among the cultures isolated from pasteurized milk samples. Twenty-five percent of the strains could only be classified as Aeromonas spp. In white cheese samples, unclassified strains were the most frequent isolates (61.5%) followed by A. hydrophila (26.9%), A. caviae (7.6%) and Aeromonas sobria (3.8%). Only strains of A. hydrophila and A. sobria showed high rate of positive results when tested for the production of hemolysin, cytotoxin, and staphylolytic activity. Heat-stable enterotoxin and autoagglutination test did not correlate as virulence factors. The presence of Aeromonas species in refrigerated food samples suggests that this microorganism could be a potential foodborne pathogen, and dairy products may represent an important vehicle of its transmission.- Published
- 1993
- Full Text
- View/download PDF
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