Skip to main content

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

Citation
Yamaguchi, S., and J. Yoshino. “Adipose Tissue Nad Biology In Obesity And Insulin Resistance: From Mechanism To Therapy.”. Bioessays : News And Reviews In Molecular, Cellular And Developmental Biology.
Center Washington University in St Louis
Author Shintaro Yamaguchi, Jun Yoshino
Keywords NAD+, NAMPT, PPARγ, SIRT1, Adipose tissue, Insulin resistance, obesity
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.

Year of Publication
2017
Journal
BioEssays : news and reviews in molecular, cellular and developmental biology
Volume
39
Issue
5
Date Published
12/2017
ISSN Number
1521-1878
DOI
10.1002/bies.201600227
Alternate Journal
Bioessays
PMID
28295415
PMCID
PMC5469033
Download citation