Effects of AMP-activated protein kinase in cerebral ischemia

被引:151
|
作者
Li, Jun [2 ]
McCullough, Louise D. [1 ,2 ]
机构
[1] Univ Connecticut, Ctr Hlth, Dept Neurol, Farmington, CT 06030 USA
[2] Univ Connecticut, Ctr Hlth, Dept Neurosci, Farmington, CT 06030 USA
来源
关键词
angiogenesis; endothelium; ischemia; neuronal metabolism; nitric oxide; statins; NITRIC-OXIDE SYNTHASE; NEUROTROPHIC FACTOR EXPRESSION; RIBOSIDE INDUCES APOPTOSIS; AORTIC ENDOTHELIAL-CELLS; IN-VIVO; GLUCOSE-UPTAKE; SKELETAL-MUSCLE; ENERGY-BALANCE; INDUCED ANGIOGENESIS; NEUROBLASTOMA-CELLS;
D O I
10.1038/jcbfm.2009.255
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AMP-activated protein kinase (AMPK) is a serine threonine kinase that is highly conserved through evolution. AMPK is found in most mammalian tissues including the brain. As a key metabolic and stress sensor/effector, AMPK is activated under conditions of nutrient deprivation, vigorous exercise, or heat shock. However, it is becoming increasingly recognized that changes in AMPK activation not only signal unmet metabolic needs, but also are involved in sensing and responding to 'cell stress', including ischemia. The downstream effect of AMPK activation is dependent on many factors, including the severity of the stressor as well as the tissue examined. This review discusses recent in vitro and in vivo studies performed in the brain/neuronal cells and vasculature that have contributed to our understanding of AMPK in stroke. Recent data on the potential role of AMPK in angiogenesis and neurogenesis and the interaction of AMPK with 3-hydroxy-3-methy-glutaryl-CoA reductase inhibitors (statins) agents are highlighted. The interaction between AMPK and nitric oxide signaling is also discussed. Journal of Cerebral Blood Flow & Metabolism (2010) 30, 480-492; doi: 10.1038/jcbfm.2009.255; published online 16 December 2009
引用
收藏
页码:480 / 492
页数:13
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