1,665 research outputs found

    ANÁLISE TERMOMECÂNICA DE ESTRUTURAS DE AÇO VIA ACOPLAMENTO MCD/MRPR

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    Quando expostos à temperatura elevada, os elementos estruturais tĂȘm sua capacidade resistente comprometida, pois as caracterĂ­sticas fĂ­sicas e de resistĂȘncia dos materiais empregados nas estruturas se deterioram com o aumento de temperatura. Nesse contexto, o presente trabalho tem como objetivo apresentar um novo mĂłdulo computacional,denominado aqui CS-ASA/FSA, capaz de realizar a anĂĄlise numĂ©rica de estruturas de aço sujeitas à temperaturas elevadas. Esse mĂłdulo utiliza o MĂ©todo dos Elementos Finitos (MEF) e a anĂĄlise inelĂĄstica Ă© baseada no MĂ©todo da RĂłtula PlĂĄstica Refinado (MRPR) acoplado ao MĂ©todo da Compatibilidade de DeformaçÔes (MCD). Esse Ășltimo mĂ©todo foi adotado para avaliar tanto a capacidade resistente da seção transversal, quanto as rigidezes axial e à flexĂŁo de estruturas de aço sob elevadas temperaturas. A construção da relação momentocurvatura se torna essencial para tal avaliação. Por fim, os resultados obtidos sĂŁo comparados aos numĂ©ricos e experimentais encontrados na literatura

    Regulation of glucose and fatty acid metabolism in skeletal muscle during contraction

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    O ciclo glicose-ĂĄcido graxo explica a preferĂȘncia do tecido muscular pelos ĂĄcidos graxos durante atividade moderada de longa duração. Em contraste, durante o exercĂ­cio de alta intensidade, hĂĄ aumento na disponibilidade e na taxa de oxidação de glicose. A produção de espĂ©cies reativas de oxigĂȘnio (EROs) durante a atividade muscular sugere que o balanço redox intracelular Ă© importante na regulação do metabolismo de lipĂ­dios/carboidratos. As EROs diminuem a atividade do ciclo de Krebs e aumentam a atividade da proteĂ­na desacopladora mitocondrial. O efeito oposto Ă© esperado durante a atividade moderada. Assim, as questĂ”es levantadas nesta revisĂŁo sĂŁo: Por que o mĂșsculo esquelĂ©tico utiliza preferencialmente os lipĂ­dios no estado basal e de atividade moderada? Por que o ciclo glicose-ĂĄcido graxo falha em exercer seus efeitos durante o exercĂ­cio intenso? Como o mĂșsculo esquelĂ©tico regula o metabolismo de lipĂ­dios e carboidratos em regime envolvendo o ciclo contração-relaxamento555303313CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO - CNPQCOORDENAÇÃO DE APERFEIÇOAMENTO DE PESSOAL DE NÍVEL SUPERIOR - CAPESFUNDAÇÃO DE AMPARO À PESQUISA DO ESTADO DE SÃO PAULO - FAPESPsem informaçãoThe glucose-fatty acid cycle explains the preference for fatty acid during moderate and long duration physical exercise. In contrast, there is a high glucose availability and oxidation rate in response to intense physical exercise. The reactive oxygen species (ROS) production during physical exercise suggests that the redox balance is important to regulate of lipids/carbohydrate metabolism. ROS reduces the activity of the Krebs cycle, and increases the activity of mitochondrial uncoupling proteins. The opposite effects happen during moderate physical activity. Thus, some issues is highlighted in the present review: Why does skeletal muscle prefer lipids in the basal and during moderate physical activity? Why does glucose-fatty acid fail to carry out their effects during intense physical exercise? How skeletal muscles regulate the lipids and carbohydrate metabolism during the contraction-relaxation cycle

    Regulation of glucose and fatty acid metabolism in skeletal muscle during contraction

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    O ciclo glicose-ĂĄcido graxo explica a preferĂȘncia do tecido muscular pelos ĂĄcidos graxos durante atividade moderada de longa duração. Em contraste, durante o exercĂ­cio de alta intensidade, hĂĄ aumento na disponibilidade e na taxa de oxidação de glicose. A produção de espĂ©cies reativas de oxigĂȘnio (EROs) durante a atividade muscular sugere que o balanço redox intracelular Ă© importante na regulação do metabolismo de lipĂ­dios/carboidratos. As EROs diminuem a atividade do ciclo de Krebs e aumentam a atividade da proteĂ­na desacopladora mitocondrial. O efeito oposto Ă© esperado durante a atividade moderada. Assim, as questĂ”es levantadas nesta revisĂŁo sĂŁo: Por que o mĂșsculo esquelĂ©tico utiliza preferencialmente os lipĂ­dios no estado basal e de atividade moderada? Por que o ciclo glicose-ĂĄcido graxo falha em exercer seus efeitos durante o exercĂ­cio intenso? Como o mĂșsculo esquelĂ©tico regula o metabolismo de lipĂ­dios e carboidratos em regime envolvendo o ciclo contração-relaxamento.The glucose-fatty acid cycle explains the preference for fatty acid during moderate and long duration physical exercise. In contrast, there is a high glucose availability and oxidation rate in response to intense physical exercise. The reactive oxygen species (ROS) production during physical exercise suggests that the redox balance is important to regulate of lipids/carbohydrate metabolism. ROS reduces the activity of the Krebs cycle, and increases the activity of mitochondrial uncoupling proteins. The opposite effects happen during moderate physical activity. Thus, some issues is highlighted in the present review: Why does skeletal muscle prefer lipids in the basal and during moderate physical activity? Why does glucose-fatty acid fail to carry out their effects during intense physical exercise? How skeletal muscles regulate the lipids and carbohydrate metabolism during the contraction-relaxation cycle

    Hydrogen peroxide production regulates the mitochondrial function in insulin resistant muscle cells: Effect of catalase overexpression

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    AbstractThe mitochondrial redox state plays a central role in the link between mitochondrial overloading and insulin resistance. However, the mechanism by which the ROS induce insulin resistance in skeletal muscle cells is not completely understood. We examined the association between mitochondrial function and H2O2 production in insulin resistant cells. Our hypothesis is that the low mitochondrial oxygen consumption leads to elevated ROS production by a mechanism associated with reduced PGC1α transcription and low content of phosphorylated CREB. The cells were transfected with either the encoded sequence for catalase overexpression or the specific siRNA for catalase inhibition. After transfection, myotubes were incubated with palmitic acid (500ÎŒM) and the insulin response, as well as mitochondrial function and fatty acid metabolism, was determined. The low mitochondrial oxygen consumption led to elevated ROS production by a mechanism associated with ÎČ-oxidation of fatty acids. Rotenone was observed to reduce the ratio of ROS production. The elevated H2O2 production markedly decreased the PGC1α transcription, an effect that was accompanied by a reduced phosphorylation of Akt and CREB. The catalase transfection prevented the reduction in the phosphorylated level of Akt and upregulated the levels of phosphorylated CREB. The mitochondrial function was elevated and H2O2 production reduced, thus increasing the insulin sensitivity. The catalase overexpression improved mitochondrial respiration protecting the cells from fatty acid-induced, insulin resistance. This effect indicates that control of hydrogen peroxide production regulates the mitochondrial respiration preventing the insulin resistance in skeletal muscle cells by a mechanism associated with CREB phosphorylation and ÎČ-oxidation of fatty acids

    The BLue Amazon Brain (BLAB): A Modular Architecture of Services about the Brazilian Maritime Territory

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    We describe the first steps in the development of an artificial agent focused on the Brazilian maritime territory, a large region within the South Atlantic also known as the Blue Amazon. The "BLue Amazon Brain" (BLAB) integrates a number of services aimed at disseminating information about this region and its importance, functioning as a tool for environmental awareness. The main service provided by BLAB is a conversational facility that deals with complex questions about the Blue Amazon, called BLAB-Chat; its central component is a controller that manages several task-oriented natural language processing modules (e.g., question answering and summarizer systems). These modules have access to an internal data lake as well as to third-party databases. A news reporter (BLAB-Reporter) and a purposely-developed wiki (BLAB-Wiki) are also part of the BLAB service architecture. In this paper, we describe our current version of BLAB's architecture (interface, backend, web services, NLP modules, and resources) and comment on the challenges we have faced so far, such as the lack of training data and the scattered state of domain information. Solving these issues presents a considerable challenge in the development of artificial intelligence for technical domains

    Medium Chain Fatty Acids Are Selective Peroxisome Proliferator Activated Receptor (PPAR) Îł Activators and Pan-PPAR Partial Agonists

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    Thiazolidinediones (TZDs) act through peroxisome proliferator activated receptor (PPAR) Îł to increase insulin sensitivity in type 2 diabetes (T2DM), but deleterious effects of these ligands mean that selective modulators with improved clinical profiles are needed. We obtained a crystal structure of PPARÎł ligand binding domain (LBD) and found that the ligand binding pocket (LBP) is occupied by bacterial medium chain fatty acids (MCFAs). We verified that MCFAs (C8–C10) bind the PPARÎł LBD in vitro and showed that they are low-potency partial agonists that display assay-specific actions relative to TZDs; they act as very weak partial agonists in transfections with PPARÎł LBD, stronger partial agonists with full length PPARÎł and exhibit full blockade of PPARÎł phosphorylation by cyclin-dependent kinase 5 (cdk5), linked to reversal of adipose tissue insulin resistance. MCFAs that bind PPARÎł also antagonize TZD-dependent adipogenesis in vitro. X-ray structure B-factor analysis and molecular dynamics (MD) simulations suggest that MCFAs weakly stabilize C-terminal activation helix (H) 12 relative to TZDs and this effect is highly dependent on chain length. By contrast, MCFAs preferentially stabilize the H2-H3/ÎČ-sheet region and the helix (H) 11-H12 loop relative to TZDs and we propose that MCFA assay-specific actions are linked to their unique binding mode and suggest that it may be possible to identify selective PPARÎł modulators with useful clinical profiles among natural products

    The impact of surgical delay on resectability of colorectal cancer: An international prospective cohort study

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    AIM: The SARS-CoV-2 pandemic has provided a unique opportunity to explore the impact of surgical delays on cancer resectability. This study aimed to compare resectability for colorectal cancer patients undergoing delayed versus non-delayed surgery. METHODS: This was an international prospective cohort study of consecutive colorectal cancer patients with a decision for curative surgery (January-April 2020). Surgical delay was defined as an operation taking place more than 4 weeks after treatment decision, in a patient who did not receive neoadjuvant therapy. A subgroup analysis explored the effects of delay in elective patients only. The impact of longer delays was explored in a sensitivity analysis. The primary outcome was complete resection, defined as curative resection with an R0 margin. RESULTS: Overall, 5453 patients from 304 hospitals in 47 countries were included, of whom 6.6% (358/5453) did not receive their planned operation. Of the 4304 operated patients without neoadjuvant therapy, 40.5% (1744/4304) were delayed beyond 4 weeks. Delayed patients were more likely to be older, men, more comorbid, have higher body mass index and have rectal cancer and early stage disease. Delayed patients had higher unadjusted rates of complete resection (93.7% vs. 91.9%, P = 0.032) and lower rates of emergency surgery (4.5% vs. 22.5%, P < 0.001). After adjustment, delay was not associated with a lower rate of complete resection (OR 1.18, 95% CI 0.90-1.55, P = 0.224), which was consistent in elective patients only (OR 0.94, 95% CI 0.69-1.27, P = 0.672). Longer delays were not associated with poorer outcomes. CONCLUSION: One in 15 colorectal cancer patients did not receive their planned operation during the first wave of COVID-19. Surgical delay did not appear to compromise resectability, raising the hypothesis that any reduction in long-term survival attributable to delays is likely to be due to micro-metastatic disease

    Causal effect of plasminogen activator inhibitor type 1 on coronary heart disease

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    Background--Plasminogen activator inhibitor type 1 (PAI-1) plays an essential role in the fibrinolysis system and thrombosis. Population studies have reported that blood PAI-1 levels are associated with increased risk of coronary heart disease (CHD). However, it is unclear whether the association reflects a causal influence of PAI-1 on CHD risk. Methods and Results--To evaluate the association between PAI-1 and CHD, we applied a 3-step strategy. First, we investigated the observational association between PAI-1 and CHD incidence using a systematic review based on a literature search for PAI-1 and CHD studies. Second, we explored the causal association between PAI-1 and CHD using a Mendelian randomization approach using summary statistics from large genome-wide association studies. Finally, we explored the causal effect of PAI-1 on cardiovascular risk factors including metabolic and subclinical atherosclerosis measures. In the systematic meta-analysis, the highest quantile of blood PAI-1 level was associated with higher CHD risk comparing with the lowest quantile (odds ratio=2.17; 95% CI: 1.53, 3.07) in an age- and sex-adjusted model. The effect size was reduced in studies using a multivariable-adjusted model (odds ratio=1.46; 95% CI: 1.13, 1.88). The Mendelian randomization analyses suggested a causal effect of increased PAI-1 level on CHD risk (odds ratio=1.22 per unit increase of log-transformed PAI-1; 95% CI: 1.01, 1.47). In addition, we also detected a causal effect of PAI-1 on elevating blood glucose and high-density lipoprotein cholesterol. Conclusions--Our study indicates a causal effect of elevated PAI-1 level on CHD risk, which may be mediated by glucose dysfunction
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