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氧化还原信号与肌肉减少症:寻找主要嫌疑人。

Redox Signaling and Sarcopenia: Searching for the Primary Suspect.

机构信息

Laboratory of Physiological Hygiene and Exercise Science, School of Kinesiology, College of Education and Human Development, University of Minnesota, 1900 University Ave, Minneapolis, MN 55455, USA.

出版信息

Int J Mol Sci. 2021 Aug 22;22(16):9045. doi: 10.3390/ijms22169045.

Abstract

Sarcopenia, the age-related decline in muscle mass and function, derives from multiple etiological mechanisms. Accumulative research suggests that reactive oxygen species (ROS) generation plays a critical role in the development of this pathophysiological disorder. In this communication, we review the various signaling pathways that control muscle metabolic and functional integrity such as protein turnover, cell death and regeneration, inflammation, organismic damage, and metabolic functions. Although no single pathway can be identified as the most crucial factor that causes sarcopenia, age-associated dysregulation of redox signaling appears to underlie many deteriorations at physiological, subcellular, and molecular levels. Furthermore, discord of mitochondrial homeostasis with aging affects most observed problems and requires our attention. The search for the primary suspect of the fundamental mechanism for sarcopenia will likely take more intense research for the secret of this health hazard to the elderly to be unlocked.

摘要

肌肉减少症是与年龄相关的肌肉质量和功能下降,源于多种病因机制。累积的研究表明,活性氧(ROS)的产生在这种病理生理紊乱的发展中起着关键作用。在本通讯中,我们回顾了控制肌肉代谢和功能完整性的各种信号通路,如蛋白质周转、细胞死亡和再生、炎症、机体损伤和代谢功能。虽然没有单一的途径可以被确定为导致肌肉减少症的最关键因素,但与年龄相关的氧化还原信号的失调似乎是许多生理、亚细胞和分子水平恶化的基础。此外,与衰老相关的线粒体动态平衡失调会影响大多数观察到的问题,需要我们关注。寻找肌肉减少症基本机制的主要嫌疑人可能需要更深入的研究,才能揭示这一老年人健康危害的秘密。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a21/8396474/6ea62a6d9e56/ijms-22-09045-g001.jpg

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