Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1602
Title: Role of sirtuins in obesity
Authors: Nijhawan P
Behl T.
Keywords: Obesity
Sirtuins
Calorie restriction
Adipogenesis
SIRT1
Issue Date: 2020
Publisher: Elsevier Ltd
Abstract: Various approaches have been made to reduce the progression of obesity and its associated disorders as it threatens the public health globally. Sirtuins (silent information regulator) is a conserved mammalian (nicotinamide adenine nucleotide) NAD+ dependent protein deacetylase considered as promising target for treating various diseases e.g., cancer and neurodegenerative disorder. It consist of seven types of sirtuins including SIRT1, SIRT2, SIRT3, SIRT4, SIRT4, SIRT5, SIRT6, SIRT7, out which SIRT1 sirtuins emerged out as putative molecule in the treatment of obesity and act as metabolic sensor of glucose and lipids in liver by using short carbon fragment viz. acetyl coenzyme A. It play key roles in regulation of gene expression, aging, insulin secretion, insulin sensitivity, mobilization of stored fat, formation of white adipose tissue and brown adipose tissue, mediate inflammatory responses in macrophage. Additionally, SIRT1 regulate adipokines expression, act as therapeutic target for type II diabetes mellitus, deacetylates histone proteins inhibit the factors required for maturation of cells. Conclusion Alteration in the above physiological processes result in the development of obesity and obesity related disorder, so SIRT1 is emerged out as therapeutic molecule for the prevention of obesity. This review demonstrates the use of sirtuins as a potent agent in the treatment of obesity and the current status focus on the therapeutic potential of sirtuins in prevention of excessive accumulation of fat in adipose tissue.
URI: 10.1016/j.obmed.2019.100156
http://hdl.handle.net/123456789/1602
Appears in Collections:Journals

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.