Mechanisms of Testosterone's Anabolic Effects on Muscle and Function: Controversies and New Insights

内分泌学 肌发生 内科学 合成代谢 肌肉肥大 睾酮(贴片) 骨骼肌 心肌细胞 生物 雄激素受体 肌肉萎缩 肌营养不良蛋白 卵泡抑素 雄激素 祖细胞 萎缩 肌萎缩 合成代谢类固醇 肌动蛋白 合成代谢剂 血管平滑肌
作者
Shalender Bhasin,Chengzhi Wang,Muni Ramanna GariSubhosh Chandra,Thiago Gagliano‐Jucá,Ravi Jasuja
出处
期刊:Endocrine Reviews [Oxford University Press]
卷期号:47 (2): 280-300 被引量:7
标识
DOI:10.1210/endrev/bnaf041
摘要

Testosterone treatment increases muscle mass, maximal voluntary muscle strength, aerobic capacity, and some measures of physical function. Activational and epigenetic mechanisms by which androgens improve muscle mass and physical performance and how to apply these anabolic effects to treat functional limitations associated with aging and disease remain incompletely understood. Testosterone treatment induces hypertrophy of type 1 and 2 muscle fibers and increases muscle progenitor cell numbers by promoting differentiation of mesenchymal progenitor cells into myogenic lineage by an androgen receptor (AR)-mediated pathway. Liganded AR binds to β-catenin, translocates into nucleus where it binds T cell factor-4, and upregulates follistatin that blocks signaling through the TGF-β pathway to promote myogenesis and inhibit adipogenesis. Testosterone increases myoblast proliferation by stimulating polyamine biosynthesis. Stimulation of GH and IGF-1 secretion, intramuscular IGF-1 receptor, and muscle protein synthesis and inhibition of muscle atrophy genes further contribute to testosterone's anabolic effects. Testosterone improves muscle bioenergetics by increasing erythrocytes, oxygen availability, tissue blood flow, and mitochondrial mass and quality. Testosterone increases blood flow by nongenomic mechanisms involving nitric oxide production and calcium and potassium channels in vascular smooth muscle. The conversion of testosterone to 5α-DHT is not required for mediating its anabolic effects. Mechanisms of testosterone's sexually dimorphic epigenetic and tissue-specific activational effects and roles of α-keto reductase and steroid 5α-reductase and 1-carbon and polyamine metabolism in testosterone's actions remain poorly understood. Strategies to translate testosterone-induced muscle mass and strength gains into patient-important improvements in functional performance and health outcomes are needed to enable its clinical applications to treat functional limitations associated with aging and disease.
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