Gilliver, Stephen C. and Ashworth, Jason J. and Mills, Stuart J. and Hardman, Matthew J. and Ashcroft, Gillian S. (2006) Androgens modulate the inflammatory response during acute wound healing. ISSN 1477-9137Full text not available from this repository.
Impaired wound healing states in the elderly lead to substantial morbidity and mortality, and a cost to the health services of over $9 billion per annum. In addition to intrinsic ageing processes that per se cause delayed healing, studies have suggested marked differences in wound repair between the sexes. We have previously reported that, castration of male mice results in a striking acceleration of local cutaneous wound healing and dampens the associated inflammatory response. In this study, we report that systemic 5-reductase inhibition, which blocks the conversion of testosterone to its more active metabolite 5-dihydrotestosterone, mimics the effects of castration in a rat model of cutaneous wound healing. The mechanisms underlying the observed effects involve a direct, cell-specific upregulation of pro-inflammatory cytokine expression by macrophages, but not fibroblasts, in response to androgens. Androgens require the transforming growth factor ß signalling intermediate Smad3 to be present in order to influence repair and local pro-inflammatory cytokine levels. That reducing 5-dihydrotestosterone levels through 5-reductase antagonism markedly accelerates healing suggests a specific target for future therapeutic intervention in impaired wound healing states in elderly males.
|Additional Information:||Full-text of this article is not available in this e-prints service. This article was originally published [following peer-review] in Journal of Cell Science, published by and copyright The Company of Biologists.|
|Divisions:||Legacy Research Institutes > Research Institute for Health and Social Change > Social Change and Well Being|
|Date Deposited:||11 Jan 2010 13:58|
|Last Modified:||01 Sep 2016 13:57|
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