Yamaguchi Shintaro, Yoshino Jun
Center for Human Nutrition, Division of Geriatrics and Nutritional Science, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Bioessays. 2017 May;39(5). doi: 10.1002/bies.201600227. Epub 2017 Mar 15.
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.
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。