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脂联素在人类肥胖和胰岛素抵抗中的作用。

The role of perilipin in human obesity and insulin resistance.

作者信息

Tai E Shyong, Ordovas Jose M

机构信息

Department of Endocrinology, Singapore General Hospital, Singapore.

出版信息

Curr Opin Lipidol. 2007 Apr;18(2):152-6. doi: 10.1097/MOL.0b013e328086aeab.

Abstract

PURPOSE OF REVIEW

More than 1.1 billion people worldwide are overweight or obese. We know that obesity is determined by a combination of environmental and genetic factors. Although hundreds of obesity candidate genes have been identified through different metabolic pathways, the fundamental basis of obesity resides with excessive storage of triacylglycerides in adipose tissue.

RECENT FINDINGS

The mechanisms that control the storage and release of triacylglycerides in lipid droplets are complex and poorly understood; yet, they are likely to be crucial to the understanding of the regulation of body weight. In this regard, the family of perilipin, adipophilin and TIP47 proteins may play key roles in obesity. It has recently been shown that variants at the perilipin locus were associated with BMI and obesity risk in females from several population studies. Moreover, the reported interactions between perilipin and dietary factors may shed light on the complex relation between dietary intake and body weight changes observed on an individual basis.

SUMMARY

These findings support an important role for PLIN as a candidate gene for obesity risk in humans as well as a modulator of dietary response to therapies aimed to reduce body weight and decrease metabolic syndrome risk.

摘要

综述目的

全球超过11亿人超重或肥胖。我们知道肥胖是由环境和遗传因素共同决定的。尽管通过不同的代谢途径已鉴定出数百个肥胖候选基因,但肥胖的根本原因在于脂肪组织中甘油三酯的过度储存。

最新发现

脂质小滴中甘油三酯储存和释放的调控机制复杂且了解甚少;然而,它们可能对于理解体重调节至关重要。在这方面,周脂素、脂肪亲和素和TIP47蛋白家族可能在肥胖中起关键作用。最近的多项人群研究表明,周脂素基因座的变异与女性的体重指数和肥胖风险相关。此外,所报道的周脂素与饮食因素之间的相互作用可能有助于解释个体饮食摄入与体重变化之间的复杂关系。

总结

这些发现支持PLIN作为人类肥胖风险候选基因以及旨在减轻体重和降低代谢综合征风险的治疗饮食反应调节剂的重要作用。

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