Androgen receptor-mediated inhibition of cutaneous wound healing

J Clin Invest. 2002 Sep;110(5):615-24. doi: 10.1172/JCI15704.

Abstract

Impaired wound healing states in the elderly lead to substantial morbidity, mortality, and a cost to the US Health Services of over $9 billion per annum. In addition to intrinsic aging per se causing delayed healing, studies have suggested marked sex-differences in wound repair. We report that castration of male mice results in a striking acceleration of local cutaneous wound healing, and is associated with a reduced inflammatory response and increased hair growth. Using a hairless mouse model, we have demonstrated that testosterone reduction stimulates the healing response not through hair follicle epithelial/mesenchymal cell proliferation, but directly via effects on wound cell populations. We suggest that endogenous testosterone inhibits the cutaneous wound healing response in males and is associated with an enhanced inflammatory response. The mechanisms underlying the observed effects involve a direct upregulation of proinflammatory cytokine expression by macrophages in response to testosterone. Blockade of androgen action systemically, via receptor antagonism, accelerates healing significantly, suggesting a specific target for future therapeutic intervention in impaired wound healing states in elderly males.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Cells, Cultured
  • Cytokines / metabolism
  • Female
  • Humans
  • Immunohistochemistry
  • Macrophages / metabolism
  • Male
  • Mice
  • Mice, Hairless
  • Mice, Inbred C57BL
  • Middle Aged
  • Monocytes / metabolism
  • Radioimmunoassay
  • Receptors, Androgen / metabolism
  • Receptors, Androgen / physiology*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Ribonucleases / metabolism
  • Sex Factors
  • Skin / metabolism*
  • Testosterone / pharmacology
  • Time Factors
  • Up-Regulation
  • Wound Healing*

Substances

  • Cytokines
  • Receptors, Androgen
  • Testosterone
  • Ribonucleases