SIRT1 Regulation Modulates Stroke Outcome

被引:32
|
作者
Petegnief, Valerie [1 ]
Planas, Anna M. [1 ]
机构
[1] Inst Invest Biomed August Pi Sunyer, Inst Biomed Res Barcelona, Spanish Res Council, Dept Brain Ischemia & Neurodegenerat, Barcelona, Spain
关键词
Sirtuin; Histone deacetylase; Endogenous neuroprotection; Stress protein; Cerebral ischemia; FOCAL CEREBRAL-ISCHEMIA; HISTONE DEACETYLASE INHIBITION; CELL-SURVIVAL; NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE; NAD(+) DEPLETION; PROTECTS NEURONS; MICE SHOW; ACETYLATION; RESVERATROL; SIRTUINS;
D O I
10.1007/s12975-013-0277-y
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Silent information regulator 1 (SIRT1) is a NAD+-dependent histone deacetylase that represses gene expression and plays a role in longevity. SIRT1 responds to diverse stress conditions and regulates metabolism in nutrient deficiency conditions; therefore, it is involved in adaptive pathways to better fulfill tissue needs in a disturbed environment. SIRT1 overexpression or activation is protective in neurodegenerative diseases. Its role in acute nervous system injury, such as brain ischemia, is emerging, but whether SIRT1 activation improves stroke outcome is still a matter of controversy. In the present review, we will document present knowledge about the contribution of SIRT1 in death/survival in cell and animal models of brain ischemia and discuss whether SIRT1 could be a valuable target for therapeutic intervention in human stroke.
引用
收藏
页码:663 / 671
页数:9
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