SIRTUIN 1 AND SIRTUIN 3: PHYSIOLOGICAL MODULATORS OF METABOLISM

被引:660
作者
Nogueiras, Ruben
Habegger, Kirk M.
Chaudhary, Nilika
Finan, Brian
Banks, Alexander S.
Dietrich, Marcelo O.
Horvath, Tamas L.
Sinclair, David A.
Pfluger, Paul T.
Tschoep, Matthias H.
机构
[1] Univ Santiago de Compostela, Dept Physiol, Sch Med, Inst Invest Sanitarias, Santiago De Compostela, Spain
[2] CIBER Fisiopatol Obesidad & Nutr CIBERobn, Santiago De Compostela, Spain
[3] Univ Cincinnati, Dept Med, Metab Dis Inst, Cincinnati, OH 45221 USA
[4] Hemholtz Ctr Munich, Inst Diabet & Obes, Munich, Germany
[5] Tech Univ Munich, Munich, Germany
[6] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
[7] Dana Farber Canc Inst, Div Metab & Chron Dis, Boston, MA 02115 USA
[8] Yale Univ, Sch Med, Comparat Med Sect, Program Cell & Neurobiol Energy Metab, New Haven, CT 06510 USA
[9] Yale Univ, Sch Med, Dept Obstet Gynecol & Reprod Sci, New Haven, CT USA
[10] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT USA
[11] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[12] Harvard Univ, Sch Med, Paul F Glenn Labs Biol Mech Aging, Boston, MA USA
关键词
FATTY-ACID OXIDATION; FOXO TRANSCRIPTION FACTORS; SMALL-MOLECULE ACTIVATORS; LIFE-SPAN EXTENSION; DNA-DAMAGE RESPONSE; STIMULATED INSULIN-SECRETION; PROTEIN DEACETYLASE ACTIVITY; INFORMATION REGULATOR 2; NAD(+) SALVAGE PATHWAY; PROMOTES CELL-SURVIVAL;
D O I
10.1152/physrev.00022.2011
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
Nogueiras R, Habegger KM, Chaudhary N, Finan B, Banks AS, Dietrich MO, Horvath TL, Sinclair DA, Pfluger PT, Tschop MH. Sirtuin 1 and Sirtuin 3: Physiological Modulators of Metabolism. Physiol Rev 92: 1479-1514, 2012; doi:10.1152/physrev.00022.2011.-The sirtuins are a family of highly conserved NAD(+)-dependent deacetylases that act as cellular sensors to detect energy availability and modulate metabolic processes. Two sirtuins that are central to the control of metabolic processes are mammalian sirtuin 1 (SIRT1) and sirtuin 3 (SIRT3), which are localized to the nucleus and mitochondria, respectively. Both are activated by high NAD(+) levels, a condition caused by low cellular energy status. By deacetylating a variety of proteins that induce catabolic processes while inhibiting anabolic processes, SIRT1 and SIRT3 coordinately increase cellular energy stores and ultimately maintain cellular energy homeostasis. Defects in the pathways controlled by SIRT1 and SIRT3 are known to result in various metabolic disorders. Consequently, activation of sirtuins by genetic or pharmacological means can elicit multiple metabolic benefits that protect mice from diet-induced obesity, type 2 diabetes, and nonalcoholic fatty liver disease.
引用
收藏
页码:1479 / 1514
页数:36
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