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脂肪量和肥胖相关基因与肝脏葡萄糖和脂质代谢。

Fat Mass and Obesity Associated () Gene and Hepatic Glucose and Lipid Metabolism.

机构信息

Division of Endocrinology and Metabolic Disease, Department of Physiology & Pathophysiology, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB R3E 0J9, Canada.

出版信息

Nutrients. 2018 Nov 1;10(11):1600. doi: 10.3390/nu10111600.

Abstract

Common genetic variants of the fat mass and obesity associated () gene are strongly associated with obesity and type 2 diabetes. FTO is ubiquitously expressed. Earlier studies have focused on the role of hypothalamic FTO in the regulation of metabolism. However, recent studies suggest that expression of hepatic FTO is regulated by metabolic signals, such as nutrients and hormones, and altered FTO levels in the liver affect glucose and lipid metabolism. This review outlines recent findings on hepatic FTO in the regulation of metabolism, with particular focus on hepatic glucose and lipid metabolism. It is proposed that abnormal activity of hepatic signaling pathways involving FTO links metabolic impairments such as obesity, type 2 diabetes and nonalcoholic fatty liver disease (NAFLD). Therefore, a better understanding of these pathways may lead to therapeutic approaches to treat these metabolic diseases by targeting hepatic FTO. The overall goal of this review is to place FTO within the context of hepatic regulation of metabolism.

摘要

肥胖相关基因(FTO)的常见遗传变异与肥胖和 2 型糖尿病密切相关。FTO 广泛表达。早期的研究集中在 FTO 在调节代谢中的作用。然而,最近的研究表明,肝脏 FTO 的表达受代谢信号(如营养物质和激素)的调节,肝脏中 FTO 水平的改变会影响葡萄糖和脂质代谢。本综述概述了 FTO 在调节代谢中的最新发现,特别关注肝脏葡萄糖和脂质代谢。据推测,涉及 FTO 的肝脏信号通路异常活动将代谢损伤(如肥胖、2 型糖尿病和非酒精性脂肪性肝病(NAFLD))联系在一起。因此,更好地了解这些通路可能会通过靶向肝脏 FTO 为治疗这些代谢疾病提供新的治疗方法。本综述的总体目标是将 FTO 置于肝脏代谢调节的背景下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a073/6266206/3552c125b957/nutrients-10-01600-g001.jpg

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