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控制肌肉质量的信号通路。

Signaling Pathways That Control Muscle Mass.

机构信息

Craft Science Inc. Toronto, ON L4J 7S2, Canada.

Veneto Institute of Molecular Medicine, via Orus 2, 35129 Padua, Italy.

出版信息

Int J Mol Sci. 2020 Jul 4;21(13):4759. doi: 10.3390/ijms21134759.

Abstract

The loss of skeletal muscle mass under a wide range of acute and chronic maladies is associated with poor prognosis, reduced quality of life, and increased mortality. Decades of research indicate the importance of skeletal muscle for whole body metabolism, glucose homeostasis, as well as overall health and wellbeing. This tissue's remarkable ability to rapidly and effectively adapt to changing environmental cues is a double-edged sword. Physiological adaptations that are beneficial throughout life become maladaptive during atrophic conditions. The atrophic program can be activated by mechanical, oxidative, and energetic distress, and is influenced by the availability of nutrients, growth factors, and cytokines. Largely governed by a transcription-dependent mechanism, this program impinges on multiple protein networks including various organelles as well as biosynthetic and quality control systems. Although modulating muscle function to prevent and treat disease is an enticing concept that has intrigued research teams for decades, a lack of thorough understanding of the molecular mechanisms and signaling pathways that control muscle mass, in addition to poor transferability of findings from rodents to humans, has obstructed efforts to develop effective treatments. Here, we review the progress made in unraveling the molecular mechanisms responsible for the regulation of muscle mass, as this continues to be an intensive area of research.

摘要

在广泛的急性和慢性疾病中,骨骼肌质量的丧失与预后不良、生活质量下降和死亡率增加有关。数十年来的研究表明,骨骼肌对于全身代谢、葡萄糖稳态以及整体健康和幸福感都非常重要。这种组织具有快速而有效地适应环境变化的显著能力,这是一把双刃剑。在萎缩状态下,对生命有益的生理适应性会变得适应不良。萎缩程序可通过机械、氧化和能量压力激活,并受营养素、生长因子和细胞因子的可用性影响。这个程序主要受转录依赖性机制调控,会影响多种蛋白质网络,包括各种细胞器以及生物合成和质量控制系统。虽然调节肌肉功能以预防和治疗疾病是一个诱人的概念,数十年来一直吸引着研究团队,但由于对控制肌肉质量的分子机制和信号通路缺乏深入了解,以及从啮齿动物到人类的研究结果可转移性差,阻碍了开发有效治疗方法的努力。在这里,我们回顾了在揭示调节肌肉质量的分子机制方面取得的进展,因为这仍然是一个密集的研究领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1cc/7369702/ea134d9ebed2/ijms-21-04759-g001.jpg

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