Anogenital Distance Plasticity in Adulthood: Implications for Its Use as a Biomarker of Fetal Androgen Action

被引:63
|
作者
Mitchell, Rod T. [1 ]
Mungall, Will [1 ]
McKinnell, Chris [1 ]
Sharpe, Richard M. [1 ]
Cruickshanks, Lyndsey [1 ]
Milne, Laura [1 ]
Smith, Lee B. [1 ]
机构
[1] Univ Edinburgh, Queens Med Res Inst, MRC, Ctr Reprod Hlth, Edinburgh EH16 4TJ, Midlothian, Scotland
基金
英国医学研究理事会; 英国惠康基金;
关键词
PROGRAMMING WINDOW; MALE INFANTS; HYPOSPADIAS; RAT; MASCULINIZATION; TESTOSTERONE; EXHIBIT; LENGTH;
D O I
10.1210/en.2014-1534
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Androgen action during the fetal masculinization programming window (MPW) determines the maximum potential for growth of androgen-dependent organs (eg, seminal vesicles, prostate, penis, and perineum) and is reflected in anogenital distance (AGD). As such, determining AGD in postnatal life has potential as a lifelong easily accessible biomarker of overall androgen action during the MPW. However, whether the perineum remains androgen responsive in adulthood and thus responds plastically to perturbed androgen drive remains unexplored. To determine this, we treated adult male rats with either the antiandrogen flutamide or the estrogen diethylstilbestrol (DES) for 5 weeks, followed by a 4-week washout period of no treatment. We determined AGD and its correlate anogenital index (AGI) (AGD relative to body weight) at weekly intervals across this period and compared these with normal adult rats (male and female), castrated male rats, and appropriate vehicle controls. These data showed that, in addition to reducing circulating testosteroneand seminal vesicle weight, castration significantly reduced AGD(by similar to 17%), demonstrating that there is a degree of plasticity in AGD in adulthood. Flutamide treatment increased circulating testosterone yet also reduced seminal vesicle weight due to local antagonism of androgen receptor. Despite this suppression, surprisingly, flutamide treatment had no effect on AGD at any time point. In contrast, although DES treatment suppressed circulating testosterone and reduced seminal vesicle weight, it also induced a significant reduction in AGD (by similar to 11%), which returned to normal 1 week after cessation of DES treatment. We conclude that AGD in adult rats exhibits a degree of plasticity, which may be mediated by modulation of local androgen/estrogen action. The implications of these findings regarding the use of AGD as a lifelong clinical biomarker of fetal androgen action are discussed.
引用
收藏
页码:24 / 31
页数:8
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