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引用次数: 40

摘要

暴饮暴食和缺乏运动再加上遗传因素在人类超重的发展中起着最重要的作用。到目前为止,身体脂肪过度积累背后的共同基因成分尚不清楚。对候选基因的研究表明,大多数与肥胖相关的基因也控制着脂肪组织的重要功能。此外,这些基因的结构变异可能在某种程度上改变脂肪组织的功能,从而促进肥胖。在人体脂肪组织中起作用并与肥胖相关的基因有:激素敏感脂肪酶、β 2和β 3肾上腺素受体、肿瘤坏死因子α、低密度脂蛋白受体、解偶联蛋白-1和过氧化物酶体增殖物激活受体γ -2。其他基因对女性肥胖最为重要(例如β 2和β 3肾上腺素受体、低密度脂蛋白受体和肿瘤坏死因子α)。其中一些基因可能通过基因-基因相互作用(例如β -肾上腺素受体和解偶联蛋白-1)或基因-环境相互作用(例如β -肾上腺素受体和体育活动)促进肥胖。很少有在脂肪组织中没有已知功能的基因显示出与过量体脂的密切联系。后者表明重要的人类肥胖基因也控制脂肪组织功能。因此,将进一步寻找肥胖基因的重点放在脂肪组织上可能是有价值的。
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Hunting for human obesity genes? Look in the adipose tissue!

Over-eating and physical inactivity in combination with genetic factors play the most important roles in the development of over weight in humans. The common genetic components behind excess accumulation of body fat are so far unknown. Studies of candidate genes indicate that most of the genes that associate with obesity control important functions of adipose tissue as well. Furthermore, structural variations in these genes may alter adipose tissue function in a way that promotes obesity. The genes which both are functional in human adipose tissue and associate with obesity are: hormone sensitive lipase, beta2 and beta3-adrenoceptors, tumor necrosis factor alpha, low density lipoprotein receptor, uncoupling protein-1 and peroxisome proliferator activated receptor gamma-2. Other genes are mostly important for obesity among women (for example beta2 -and beta3-adrenoceptors, low density lipoprotein receptor and tumor necrosis factor alpha). Some of these genes may promote obesity by gene-gene interactions (for example beta3-adrenoceptors and uncoupling protein-1) or gene-environmental interactions (for example beta2-adrenoceptors and physical activity). Few genes with no known function in adipose tissue have shown a firm association with excess body fat. The latter suggests that the important human obesity genes also control adipose tissue function. Therefore it might be of value to focus the further hunt for obesity genes on the fat tissue.

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Concept of fat balance in human obesity revisited with particular reference to de novo lipogenesis. Role of energy charge and AMP-activated protein kinase in adipocytes in the control of body fat stores. Role of glucocorticoids in the physiopathology of excessive fat deposition and insulin resistance. Fat storage in pancreas and in insulin-sensitive tissues in pathogenesis of type 2 diabetes. Ectopic fat storage in heart, blood vessels and kidneys in the pathogenesis of cardiovascular diseases.
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