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胰岛素抵抗与肌肉减少症:常见共病之间的机制联系

Insulin resistance and sarcopenia: mechanistic links between common co-morbidities.

作者信息

Cleasby Mark E, Jamieson Pauline M, Atherton Philip J

机构信息

Department of Comparative Biomedical SciencesRoyal Veterinary College, University of London, London, UK

Centre for Cardiovascular ScienceQueen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.

出版信息

J Endocrinol. 2016 May;229(2):R67-81. doi: 10.1530/JOE-15-0533. Epub 2016 Mar 1.

Abstract

Insulin resistance (IR) in skeletal muscle is a key defect mediating the link between obesity and type 2 diabetes, a disease that typically affects people in later life. Sarcopenia (age-related loss of muscle mass and quality) is a risk factor for a number of frailty-related conditions that occur in the elderly. In addition, a syndrome of 'sarcopenic obesity' (SO) is now increasingly recognised, which is common in older people and is applied to individuals that simultaneously show obesity, IR and sarcopenia. Such individuals are at an increased risk of adverse health events compared with those who are obese or sarcopenic alone. However, there are no licenced treatments for sarcopenia or SO, the syndrome is poorly defined clinically and the mechanisms that might explain a common aetiology are not yet well characterised. In this review, we detail the nature and extent of the clinical syndrome, highlight some of the key physiological processes that are dysregulated and discuss some candidate molecular pathways that could be implicated in both metabolic and anabolic defects in skeletal muscle, with an eye towards future therapeutic options. In particular, the potential roles of Akt/mammalian target of rapamycin signalling, AMP-activated protein kinase, myostatin, urocortins and vitamin D are discussed.

摘要

骨骼肌中的胰岛素抵抗(IR)是介导肥胖与2型糖尿病之间联系的关键缺陷,2型糖尿病通常影响老年人。肌肉减少症(与年龄相关的肌肉质量和质量损失)是老年人发生的许多与虚弱相关疾病的危险因素。此外,“肌少症性肥胖”(SO)综合征现在越来越受到认可,它在老年人中很常见,适用于同时表现出肥胖、IR和肌肉减少症的个体。与仅肥胖或仅患肌肉减少症的个体相比,这类个体发生不良健康事件的风险更高。然而,目前尚无针对肌肉减少症或SO的获批治疗方法,该综合征在临床上定义不明确,可能解释共同病因的机制也尚未得到充分表征。在本综述中,我们详细阐述了临床综合征的性质和程度,强调了一些失调的关键生理过程,并讨论了一些可能与骨骼肌代谢和合成代谢缺陷相关的候选分子途径,着眼于未来的治疗选择。特别讨论了Akt/雷帕霉素哺乳动物靶标信号传导、AMP活化蛋白激酶、肌肉生长抑制素、尿皮质素和维生素D的潜在作用。

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