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Mitochondrial Dysregulation in the Pathogenesis of Diabetes: Potential for Mitochondrial Biogenesis-Mediated Interventions

机译:糖尿病发病机制中的线粒体失调:线粒体生物发生介导的干预的潜力。

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摘要

Muscle mitochondrial metabolism is a tightly controlled process that involves the coordination of signaling pathways and factors from both the nuclear and mitochondrial genomes. Perhaps the most important pathway regulating metabolism in muscle is mitochondrial biogenesis. In response to physiological stimuli such as exercise, retrograde signaling pathways are activated that allow crosstalk between the nucleus and mitochondria, upregulating hundreds of genes and leading to higher mitochondrial content and increased oxidation of substrates. With type 2 diabetes, these processes can become deregulated and the ability of the cell to respond to nutrient and energy fluctuations is diminished. This, coupled with reduced mitochondrial content and altered mitochondrial morphology, has been directly linked to the pathogenesis of this disease. In this paper, we will discuss our current understanding of mitochondrial dysregulation in skeletal muscle as it relates to type 2 diabetes, placing particular emphasis on the pathways of mitochondrial biogenesis and mitochondrial dynamics, and the therapeutic value of exercise and other interventions.
机译:肌肉线粒体代谢是一个严格控制的过程,涉及信号通路和来自核和线粒体基因组的因素的协调。调节肌肉代谢的最重要途径可能是线粒体生物发生。响应诸如运动等生理刺激,逆行信号通路被激活,允许细胞核与线粒体之间发生串扰,上调数百种基因并导致更高的线粒体含量和底物氧化。对于2型糖尿病,这些过程可能变得失控,并且细胞对养分和能量波动的反应能力也会降低。这与线粒体含量减少和线粒体形态改变相结合,已直接与该疾病的发病机理有关。在本文中,我们将讨论我们目前对骨骼肌线粒体失调的了解,因为它与2型糖尿病有关,特别强调线粒体生物发生和线粒体动力学的途径以及运动和其他干预措施的治疗价值。

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