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Endocrine reviews

March 1, 2026 · via Europe PMC

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

Bhasin S, Wang C, Chandra MS, Gagliano-Jucá T, Jasuja R.

ReviewAbstract only — full text under license

AI summary — for doctors, generated from the abstract only

This review details the mechanisms behind testosterone's anabolic effects on muscle and highlights the need to translate muscle gains into meaningful functional improvements.

What was studied

A narrative review of activational and epigenetic mechanisms by which testosterone increases muscle mass, strength, and physical function.

Key findings

  • Testosterone induces type 1 and 2 fiber hypertrophy and promotes myogenic differentiation via androgen receptor-β-catenin-follistatin signaling
  • It stimulates polyamine biosynthesis, GH/IGF-1 signaling, and muscle protein synthesis
  • It improves muscle bioenergetics via erythrocytes, blood flow, and mitochondria
  • Conversion to DHT is not required for anabolic effects

Clinical relevance

Mechanistic overview; the authors note strategies are still needed to turn muscle gains into patient-important functional outcomes.

Who should care

Endocrinology

Limitations

Narrative review; evidence selection methods are not described in the abstract.

Testosterone builds muscle through multiple pathways, but functional benefits still need to be established.

This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.

Abstract

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.

DOI

10.1210/endrev/bnaf041

PMID

41355050

Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.

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