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Critical androgen-sensitive periods of rat penis and clitoris development
Androgen control of penis development/growth is unclear. In rats, androgen action in a foetal ‘masculinisation programming window’ (MPW; e15.5–e18.5)’ predetermines penile length and hypospadias occurrence. This has implications for humans (e.g. micropenis). Our studies aimed to establish in rats wh...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Blackwell Publishing Ltd
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816361/ https://www.ncbi.nlm.nih.gov/pubmed/19656234 http://dx.doi.org/10.1111/j.1365-2605.2009.00978.x |
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author | Welsh, Michelle MacLeod, David J Walker, Marion Smith, Lee B Sharpe, Richard M |
author_facet | Welsh, Michelle MacLeod, David J Walker, Marion Smith, Lee B Sharpe, Richard M |
author_sort | Welsh, Michelle |
collection | PubMed |
description | Androgen control of penis development/growth is unclear. In rats, androgen action in a foetal ‘masculinisation programming window’ (MPW; e15.5–e18.5)’ predetermines penile length and hypospadias occurrence. This has implications for humans (e.g. micropenis). Our studies aimed to establish in rats when androgen action/administration affects development/growth of the penis and if deficits in MPW androgen action were rescuable postnatally. Thus, pregnant rats were treated with flutamide during the MPW ± postnatal testosterone propionate (TP) treatment. To assess penile growth responsiveness, rats were treated with TP in various time windows (late foetal, neonatal through early puberty, puberty onset, or combinations thereof). Phallus length, weight, and morphology, hypospadias and anogenital distance (AGD) were measured in mid-puberty (d25) or adulthood (d90) in males and females, plus serum testosterone in adult males. MPW flutamide exposure reduced adult penile length and induced hypospadias dose-dependently; this was not rescued by postnatal TP treatment. In normal rats, foetal (e14.5–e21.5) TP exposure did not affect male penis size but increased female clitoral size. In males, TP exposure from postnatal d1–24 or at puberty (d15–24), increased penile length at d25, but not ultimately in adulthood. Foetal + postnatal TP (e14–postnatal d24) increased penile size at d25 but reduced it at d90 (due to reduced endogenous testosterone). In females, this treatment caused the biggest increase in adult clitoral size but, unlike in males, phallus size was unaffected by TP during puberty (d15–24). Postnatal TP treatment advanced penile histology at d25 to more resemble adult histology. AGD strongly correlated with final penis length. It is concluded that adult penile size depends critically on androgen action during the MPW but subsequent growth depends on later androgen exposure. Foetal and/or postnatal TP exposure does not increase adult penile size above its ‘predetermined’ length though its growth towards this maximum is advanced by peripubertal TP treatment. |
format | Text |
id | pubmed-2816361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-28163612010-02-12 Critical androgen-sensitive periods of rat penis and clitoris development Welsh, Michelle MacLeod, David J Walker, Marion Smith, Lee B Sharpe, Richard M Int J Androl Original Articles Androgen control of penis development/growth is unclear. In rats, androgen action in a foetal ‘masculinisation programming window’ (MPW; e15.5–e18.5)’ predetermines penile length and hypospadias occurrence. This has implications for humans (e.g. micropenis). Our studies aimed to establish in rats when androgen action/administration affects development/growth of the penis and if deficits in MPW androgen action were rescuable postnatally. Thus, pregnant rats were treated with flutamide during the MPW ± postnatal testosterone propionate (TP) treatment. To assess penile growth responsiveness, rats were treated with TP in various time windows (late foetal, neonatal through early puberty, puberty onset, or combinations thereof). Phallus length, weight, and morphology, hypospadias and anogenital distance (AGD) were measured in mid-puberty (d25) or adulthood (d90) in males and females, plus serum testosterone in adult males. MPW flutamide exposure reduced adult penile length and induced hypospadias dose-dependently; this was not rescued by postnatal TP treatment. In normal rats, foetal (e14.5–e21.5) TP exposure did not affect male penis size but increased female clitoral size. In males, TP exposure from postnatal d1–24 or at puberty (d15–24), increased penile length at d25, but not ultimately in adulthood. Foetal + postnatal TP (e14–postnatal d24) increased penile size at d25 but reduced it at d90 (due to reduced endogenous testosterone). In females, this treatment caused the biggest increase in adult clitoral size but, unlike in males, phallus size was unaffected by TP during puberty (d15–24). Postnatal TP treatment advanced penile histology at d25 to more resemble adult histology. AGD strongly correlated with final penis length. It is concluded that adult penile size depends critically on androgen action during the MPW but subsequent growth depends on later androgen exposure. Foetal and/or postnatal TP exposure does not increase adult penile size above its ‘predetermined’ length though its growth towards this maximum is advanced by peripubertal TP treatment. Blackwell Publishing Ltd 2010-02 /pmc/articles/PMC2816361/ /pubmed/19656234 http://dx.doi.org/10.1111/j.1365-2605.2009.00978.x Text en Journal compilation © 2010 European Academy of Andrology http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Articles Welsh, Michelle MacLeod, David J Walker, Marion Smith, Lee B Sharpe, Richard M Critical androgen-sensitive periods of rat penis and clitoris development |
title | Critical androgen-sensitive periods of rat penis and clitoris development |
title_full | Critical androgen-sensitive periods of rat penis and clitoris development |
title_fullStr | Critical androgen-sensitive periods of rat penis and clitoris development |
title_full_unstemmed | Critical androgen-sensitive periods of rat penis and clitoris development |
title_short | Critical androgen-sensitive periods of rat penis and clitoris development |
title_sort | critical androgen-sensitive periods of rat penis and clitoris development |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816361/ https://www.ncbi.nlm.nih.gov/pubmed/19656234 http://dx.doi.org/10.1111/j.1365-2605.2009.00978.x |
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