Cross-talk between SIRT1 and endocrine factors: effects on energy homeostasis

被引:25
作者
Quinones, Mar [1 ,2 ]
Al-Massadi, Omar [1 ,2 ]
Ferno, Johan [3 ]
Nogueiras, Ruben [1 ,2 ]
机构
[1] Univ Santiago de Compostela, CIBER Fisiopatol Obesidad & Nutr CIBERobn, Sch Med CIMUS, Dept Physiol,Inst Invest Sanitaria IDIS, Santiago De Compostela 15782, A Coruna, Spain
[2] Univ Santiago de Compostela, CIBER Fisiopatol Obesidad & Nutr CIBERobn, Sch Med CIMUS, Dept Physiol,Inst Invest Sanitaria IDIS, Santiago De Compostela 15782, Spain
[3] Univ Bergen, KG Jebsen Ctr Diabet Res, Dept Clin Sci, Bergen, Norway
关键词
Food intake; Hormones; Insulin; Obesity; SIRT1; FATTY-ACID-METABOLISM; REGULATES INSULIN-SECRETION; PANCREATIC BETA-CELLS; HEPATIC GLUCONEOGENIC GENES; TRANSCRIPTION FACTOR FKHR; EXTENDS LIFE-SPAN; CALORIE RESTRICTION; THYROID-HORMONE; ADIPOSE-TISSUE; UNCOUPLING PROTEIN-2;
D O I
10.1016/j.mce.2014.08.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mammalian sirtuins (SIRT1-7) are a family of highly conserved nicotine adenine dinucleotide (NAD(+))-dependent deacetylases that act as cellular sensors to detect energy availability. SIRT1 is a multifaceted protein that is involved in a wide variety of cellular processes. SIRT1 is activated in response to caloric restriction, acting on multiple targets in a wide range of tissues. SIRT1 regulates the role of multiple hormones implicated in energy balance, including glucose and lipid metabolism. Here, we review the relevant role of SIRT1 as a mediator of endocrine function of several hormones to modulate energy balance. In addition, we analyze the potential of targeting SIRT1 for the treatment of obesity and type 2 diabetes mellitus. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:42 / 50
页数:9
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