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首页> 外文期刊>American Journal of Physiology >GPCRs get fatty: the role of G protein-coupled receptor signaling in the development and progression of nonalcoholic fatty liver disease
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GPCRs get fatty: the role of G protein-coupled receptor signaling in the development and progression of nonalcoholic fatty liver disease

机译:GPCR获得脂肪:G蛋白偶联受体信号传导在非酒精性脂肪肝病的开发和进展中的作用

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摘要

Nonalcoholic fatty liver disease (NAFLD), characterized by the abnormal deposition of lipids within the liver not due to alcohol consumption, is a growing epidemic affecting over 30% of the United States population. Both simple fatty liver and its more severe counterpart, nonalcoholic steatohepatitis, represent one of the most common forms of liver disease. Recently, several G protein-coupled receptors have emerged as targets for therapeutic intervention for these disorders. These include those with known hepatic function as well as those involved in global metabolic regulation. In this review, we highlight these emerging therapeutic targets, focusing on several common themes including their activation by microbial metabolites, stimulatory effect on insulin and incretin secretion, and contribution to glucose tolerance. The overlap in ligands, localization, and downstream effects of activation indicate the interdependent nature of these receptors and highlight the importance of this signaling family in the development and prevention of NAFLD.
机译:非酒精性脂肪性肝病(NAFLD)是一种日益严重的流行病,其特征是肝脏内脂质的异常沉积,而不是由于饮酒所致,影响着超过30%的美国人口。单纯性脂肪肝和更严重的非酒精性脂肪性肝炎都是最常见的肝病之一。最近,一些G蛋白偶联受体已成为这些疾病治疗干预的靶点。这些患者包括已知肝功能的患者以及参与全球代谢调节的患者。在这篇综述中,我们重点介绍了这些新出现的治疗靶点,重点介绍了几个常见的主题,包括它们被微生物代谢产物激活,对胰岛素和肠促胰岛素分泌的刺激作用,以及对糖耐量的贡献。配体的重叠、定位和激活的下游效应表明了这些受体的相互依赖性,并强调了该信号家族在NAFLD发展和预防中的重要性。

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