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骨骼肌自噬及其在肌肉减少症和机体衰老中的作用。

Skeletal muscle autophagy and its role in sarcopenia and organismal aging.

机构信息

Department of Developmental Neurobiology, Division of Developmental Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Department of Developmental Neurobiology, Division of Developmental Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

出版信息

Curr Opin Pharmacol. 2017 Jun;34:1-6. doi: 10.1016/j.coph.2017.03.009. Epub 2017 Apr 10.

Abstract

Sarcopenia, the loss of skeletal muscle mass and strength in the aged, is an important medical condition but its etiology is incompletely understood. Because autophagy promotes myofiber atrophy in the young, it was believed that autophagy inhibition would prevent sarcopenia. However, recent studies have revealed that autophagy actually maintains muscle mass and that its function declines during muscle aging. Consistently, boosting basal autophagy protects from age-related muscle dysfunction by promoting the selective degradation of misfolded proteins and dysfunctional organelles. Conversely, autophagy inhibition leads to loss of muscle strength and induces a maladaptive stress response responsible for myofiber atrophy in the aged. In addition to cell-autonomous effects, muscle autophagy and associated signaling pathways induce systemic responses in other aging tissues by modulating the expression and secretion of myokines. We propose that myokines and pharmacologic interventions that boost selective autophagy may prevent sarcopenia, delay systemic aging, and extend health span.

摘要

肌肉减少症,即老年人骨骼肌质量和力量的丧失,是一种重要的医学病症,但病因尚未完全阐明。由于自噬会促进年轻个体的肌纤维萎缩,因此人们曾认为抑制自噬可以预防肌肉减少症。然而,最近的研究表明,自噬实际上可以维持肌肉质量,并且其功能在肌肉衰老过程中会下降。一致地,通过促进错误折叠的蛋白质和功能失调的细胞器的选择性降解,基础自噬的增强可以保护免受与年龄相关的肌肉功能障碍。相反,自噬抑制会导致肌肉力量丧失,并诱导一种适应性应激反应,导致老年人的肌纤维萎缩。除了细胞自主效应外,肌肉自噬和相关信号通路通过调节肌因子的表达和分泌,在其他衰老组织中引发全身反应。我们提出,肌因子和增强选择性自噬的药物干预可能预防肌肉减少症、延缓全身衰老并延长健康寿命。

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