肌肉肥大
核糖体生物发生
骨骼肌
mTORC1型
生物
翻译(生物学)
神经科学
细胞生物学
内分泌学
信号转导
PI3K/AKT/mTOR通路
核糖体
遗传学
核糖核酸
基因
信使核糖核酸
作者
Michael D. Roberts,John J. McCarthy,Troy A. Hornberger,Stuart M. Phillips,Abigail L. Mackey,Gustavo A. Nader,Marni D. Boppart,Andreas N. Kavazis,Paul T. Reidy,Riki Ogasawara,Cleiton Augusto Libardi,Carlos Ugrinowitsch,Frank W. Booth,Karyn A. Esser
标识
DOI:10.1152/physrev.00039.2022
摘要
Mechanisms underlying mechanical overload-induced skeletal muscle hypertrophy have been extensively researched since the landmark report by Morpurgo (1897) of “work-induced hypertrophy” in dogs that were treadmill trained. Much of the preclinical rodent and human resistance training research to date supports that involved mechanisms include enhanced mammalian/mechanistic target of rapamycin complex 1 (mTORC1) signaling, an expansion in translational capacity through ribosome biogenesis, increased satellite cell abundance and myonuclear accretion, and postexercise elevations in muscle protein synthesis rates. However, several lines of past and emerging evidence suggest that additional mechanisms that feed into or are independent of these processes are also involved. This review first provides a historical account of how mechanistic research into skeletal muscle hypertrophy has progressed. A comprehensive list of mechanisms associated with skeletal muscle hypertrophy is then outlined, and areas of disagreement involving these mechanisms are presented. Finally, future research directions involving many of the discussed mechanisms are proposed.
科研通智能强力驱动
Strongly Powered by AbleSci AI