AMP-activated protein kinase: implications on ischemic diseases

被引:27
|
作者
Ahn, Yong-Joo [1 ,2 ]
Kim, Hwewon [1 ,2 ]
Lim, Heejin [3 ]
Lee, Max [1 ,2 ]
Kang, Yuhyun [1 ,2 ]
Moon, SangJun [3 ]
Kim, Hyeon Soo [4 ]
Kim, Hyung-Hwan [1 ,2 ]
机构
[1] Brigham & Womens Hosp, Dept Med, Vasc Med Res Unit, Cambridge, MA 02139 USA
[2] Harvard Univ, Sch Med, Cambridge, MA 02139 USA
[3] DGIST, Dept Robot Engn, Taegu 700742, South Korea
[4] Korea Univ, Coll Med, Dept Anat, Seoul 136705, South Korea
关键词
AMPK; CaMKK beta; Ischemia; LKBI; NITRIC-OXIDE SYNTHASE; ENDOTHELIAL-CELLS; UPSTREAM KINASE; SKELETAL-MUSCLE; BETA; ANGIOGENESIS; ADIPONECTIN; INHIBITION; METFORMIN; BINDING;
D O I
10.5483/BMBRep.2012.45.9.169
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ischemia is a blockage of blood supply due to an embolism or a hemorrhage in a blood vessel. When an organ cannot receive oxygenated blood and can therefore no longer replenish its blood supply due to ischemia, stresses, such as the disruption of blood glucose homeostasis, hypoglycemia and hypoxia, activate the AMPK complex. LKB1 and CaMKK beta are essential activators of the AMPK signaling pathway. AMPK triggers proangiogenic effects through the eNOS protein in tissues with ischemic conditions, where cells are vulnerable to apoptosis, autophagy and necrosis. The AMPK complex acts to restore blood glucose levels and ATP levels back to homeostasis. This review will discuss AMPK, as well as its key activators (LKB1 and CaMKK beta), as a central energy regulator and evaluate the upstream and downstream regulating pathways of AMPK. We will also discuss how we can control this important enzyme in ischemic conditions to prevent harmful effects in patients with vascular damage. [BMB Reports 2012; 45(9): 489-495]
引用
收藏
页码:489 / 495
页数:7
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