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PGC-1α与运动:对抗胰岛素抵抗的重要伙伴

PGC-1alpha and exercise: important partners in combating insulin resistance.

作者信息

Russell Aaron P

机构信息

Clinique romande de réadaptation SUVA Care, Sion, Switzerland.

出版信息

Curr Diabetes Rev. 2005 May;1(2):175-81. doi: 10.2174/1573399054022811.

DOI:10.2174/1573399054022811
PMID:18220593
Abstract

Diabetes and obesity are characterised by an impairment in mitochondrial function resulting in a decrease in glucose and fatty acid oxidation, respiration and an increase in intramuscular triglycerides (IMTG's) and insulin resistance. Peroxisome proliferator-activated receptor (PPAR)-gamma coactivator 1alpha (PGC-1alpha) is a nuclear transcriptional coactivator which regulates several important metabolic processes including, mitochondrial biogenesis, adaptive thermogenesis, respiration, insulin secretion and gluconeogenesis. In addition, PGC-1alpha has been shown to increase the percentage of oxidative type I muscle fibres, with the latter responsible for the majority of insulin stimulated glucose uptake. PGC-1alpha also co-activates PPAR's alpha, beta/delta and gamma which are important transcription factors of genes regulating lipid and glucose metabolism. Exercise causes mitochondrial biogenesis, improves skeletal muscle fatty acid oxidation capacity and insulin sensitivity, therefore making it an important intervention for the treatment of insulin resistance. The expression of PGC-1alpha mRNA is reduced in diabetic subjects, however, it is rapidly induced in response to interventions which signal alterations in metabolic requirements, such as exercise. Because of the important role of PGC-1alpha in the control of energy metabolism and insulin sensitivity, it is seen as a candidate factor in the etiology of type 2 diabetes and a drug target for its therapeutic treatment.

摘要

糖尿病和肥胖的特征是线粒体功能受损,导致葡萄糖和脂肪酸氧化、呼吸作用降低,肌肉内甘油三酯(IMTG)增加以及胰岛素抵抗增强。过氧化物酶体增殖物激活受体(PPAR)-γ共激活因子1α(PGC-1α)是一种核转录共激活因子,它调节多个重要的代谢过程,包括线粒体生物合成、适应性产热、呼吸作用、胰岛素分泌和糖异生。此外,PGC-1α已被证明可增加氧化型I型肌纤维的比例,后者负责大部分胰岛素刺激的葡萄糖摄取。PGC-1α还共同激活PPAR的α、β/δ和γ,它们是调节脂质和葡萄糖代谢基因的重要转录因子。运动可导致线粒体生物合成,提高骨骼肌脂肪酸氧化能力和胰岛素敏感性,因此使其成为治疗胰岛素抵抗的重要干预措施。然而,糖尿病患者中PGC-1α mRNA的表达降低,但在响应诸如运动等表明代谢需求改变的干预措施时,其表达会迅速被诱导。由于PGC-1α在能量代谢和胰岛素敏感性控制中的重要作用,它被视为2型糖尿病病因中的一个候选因素及其治疗的药物靶点。

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