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运动训练对衰老骨骼肌胰岛素抵抗的影响:聚焦于肌肉神经酰胺。

Influence of Exercise Training on Skeletal Muscle Insulin Resistance in Aging: Spotlight on Muscle Ceramides.

机构信息

Department of Kinesiology and Health, Miami University, 420 S Oak St, Oxford, OH 45056, USA.

Departments of Physical Therapy and Athletic Training, University of Utah, 520 Wakara Way, Salt Lake City, Utah, 84018, USA.

出版信息

Int J Mol Sci. 2020 Feb 22;21(4):1514. doi: 10.3390/ijms21041514.

Abstract

Intramuscular lipid accumulation has been associated with insulin resistance (IR), aging, diabetes, dyslipidemia, and obesity. A substantial body of evidence has implicated ceramides, a sphingolipid intermediate, as potent antagonists of insulin action that drive insulin resistance. Indeed, genetic mouse studies that lower ceramides are potently insulin sensitizing. Surprisingly less is known about how physical activity (skeletal muscle contraction) regulates ceramides, especially in light that muscle contraction regulates insulin sensitivity. The purpose of this review is to critically evaluate studies (rodent and human) concerning the relationship between skeletal muscle ceramides and IR in response to increased physical activity. Our review of the literature indicates that chronic exercise reduces ceramide levels in individuals with obesity, diabetes, or hyperlipidemia. However, metabolically healthy individuals engaged in increased physical activity can improve insulin sensitivity independent of changes in skeletal muscle ceramide content. Herein we discuss these studies and provide context regarding the technical limitations (e.g., difficulty assessing the myriad ceramide species, the challenge of obtaining information on subcellular compartmentalization, and the paucity of flux measurements) and a lack of mechanistic studies that prevent a more sophisticated assessment of the ceramide pathway during increased contractile activity that lead to divergences in skeletal muscle insulin sensitivity.

摘要

肌肉内脂质积累与胰岛素抵抗(IR)、衰老、糖尿病、血脂异常和肥胖有关。大量证据表明,神经酰胺是一种鞘脂中间产物,是一种有效的胰岛素作用拮抗剂,可导致胰岛素抵抗。事实上,降低神经酰胺的基因敲除小鼠研究具有很强的胰岛素增敏作用。令人惊讶的是,关于体力活动(骨骼肌收缩)如何调节神经酰胺的知识较少,尤其是在肌肉收缩调节胰岛素敏感性的情况下。本文的目的是批判性地评估关于骨骼肌神经酰胺与体力活动增加时的 IR 之间关系的研究(啮齿动物和人类)。我们对文献的回顾表明,慢性运动可降低肥胖、糖尿病或高脂血症患者的神经酰胺水平。然而,进行更多体育活动的代谢健康个体可以改善胰岛素敏感性,而不会改变骨骼肌神经酰胺含量。在此,我们讨论了这些研究,并提供了关于技术限制(例如,评估众多神经酰胺种类的困难,获得关于亚细胞区室化信息的挑战,以及缺乏通量测量)和缺乏机制研究的背景信息,这些研究限制了对增加收缩活性期间神经酰胺途径的更复杂评估,导致骨骼肌胰岛素敏感性的差异。

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