AMP-activated protein kinase and the metabolic syndrome

被引:76
作者
Fryer, LGD [1 ]
Carling, D [1 ]
机构
[1] Univ London Imperial Coll Sci & Technol, Hammersmith Hosp, Cellular Stress Grp, MRC Clin Sci Ctr, London W12 0NN, England
关键词
AMP-activated protein kinase; energy homoeostasis; fatty acid oxidation; glucose uptake; LKB1; metabolic syndrome;
D O I
10.1042/BST0330362
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
The occurrence of Type II (non-insulin-dependent) diabetes and obesity and their associated morbidities continue to increase and they are rapidly reaching epidemic proportions. AMPK (AMP-activated protein kinase) was initially thought of as an intracellular 'fuel gauge' responding to a decrease in the level of ATP by increasing energy production and decreasing energy utilization. Recent studies have shown that AMPK plays a role in controlling the whole body energy homoeostasis, including the regulation of plasma glucose levels, fatty acid oxidation and glycogen metabolism. in addition to its effects on the periphery, AMPK has been found to play a key role in the control of food intake through its regulation by hormones, including leptin, within the hypothalamus. The control of AMPK activity, therefore, provides an attractive target for therapeutic intervention in metabolic disorders such as obesity and Type II diabetes. indeed, a number of physiological and pharmacological factors that are beneficial in these disorders have been shown to act, at least in part, through the activation of AMPK.
引用
收藏
页码:362 / 366
页数:5
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