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肥胖与胰岛素抵抗中的脂肪组织NAD生物学:从机制到治疗

Adipose tissue NAD biology in obesity and insulin resistance: From mechanism to therapy.

作者信息

Yamaguchi Shintaro, Yoshino Jun

机构信息

Center for Human Nutrition, Division of Geriatrics and Nutritional Science, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.

出版信息

Bioessays. 2017 May;39(5). doi: 10.1002/bies.201600227. Epub 2017 Mar 15.

Abstract

Nicotinamide adenine dinucleotide (NAD ) biosynthetic pathway, mediated by nicotinamide phosphoribosyltransferase (NAMPT), a key NAD biosynthetic enzyme, plays a pivotal role in controlling many biological processes, such as metabolism, circadian rhythm, inflammation, and aging. Over the past decade, NAMPT-mediated NAD biosynthesis, together with its key downstream mediator, namely the NAD -dependent protein deacetylase SIRT1, has been demonstrated to regulate glucose and lipid metabolism in a tissue-dependent manner. These discoveries have provided novel mechanistic and therapeutic insights into obesity and its metabolic complications, such as insulin resistance, an important risk factor for developing type 2 diabetes and cardiovascular disease. This review will focus on the importance of adipose tissue NAMPT-mediated NAD biosynthesis and SIRT1 in the pathophysiology of obesity and insulin resistance. We will also critically explore translational and clinical aspects of adipose tissue NAD biology.

摘要

烟酰胺腺嘌呤二核苷酸(NAD)生物合成途径由关键的NAD生物合成酶烟酰胺磷酸核糖基转移酶(NAMPT)介导,在控制许多生物过程中发挥着关键作用,如代谢、昼夜节律、炎症和衰老。在过去十年中,NAMPT介导的NAD生物合成及其关键的下游介质,即NAD依赖性蛋白脱乙酰酶SIRT1,已被证明以组织依赖性方式调节葡萄糖和脂质代谢。这些发现为肥胖及其代谢并发症,如胰岛素抵抗,提供了新的机制和治疗见解,胰岛素抵抗是发展2型糖尿病和心血管疾病的重要危险因素。本综述将重点关注脂肪组织中NAMPT介导的NAD生物合成和SIRT1在肥胖和胰岛素抵抗病理生理学中的重要性。我们还将批判性地探讨脂肪组织NAD生物学的转化和临床方面。

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