Jackson Leslie M, Timmer Kathleen M, Foster Douglas L
Reproductive Sciences Program, Department of Obstetrics and Gynecology, University of Michigan, 300 North Ingalls Room 1135, Ann Arbor, Michigan 48109, USA.
Endocrinology. 2008 Aug;149(8):4200-8. doi: 10.1210/en.2007-1382. Epub 2008 May 1.
Testicular steroids during midgestation sexually differentiate the steroid feedback mechanisms controlling GnRH secretion in sheep. To date, the actions of the estrogenic metabolites in programming neuroendocrine function have been difficult to study because exogenous estrogens disrupt maternal uterine function. We developed an approach to study the prenatal actions of estrogens by coadministering testosterone (T) and the androgen receptor antagonist flutamide, and tested the hypothesis that prenatal androgens program estradiol inhibitory feedback control of GnRH secretion to defeminize (advance) the timing of the pubertal increase in LH. Pregnant sheep were either untreated or treated with T, dihydrotestosterone (DHT) (a nonaromatizable androgen), or T plus flutamide from d 30-90 of gestation. To study the postnatal response to steroid negative feedback, lambs were gonadectomized and estradiol-replaced, and concentrations of LH were monitored in twice-weekly blood samples. Although T and DHT produced penile and scrotal development in females, the external genitalia of T plus flutamide offspring remained phenotypically female, regardless of genetic sex. Untreated females and females and males treated with T plus flutamide exhibited a pubertal increase in circulating LH at 26.4+/-0.5, 26.0+/-0.7, and 22.4+/-1.6 wk of age, respectively. In females exposed to prenatal androgens, the LH increase was advanced (T: 12.0+/-2.6 wk; DHT: 15.0+/-2.6 wk). These results demonstrate the usefulness of combining T and antiandrogen treatments as an approach to increasing prenatal exposure to estradiol. Importantly, the findings support our hypothesis that prenatal androgens program sensitivity to the negative feedback actions of estradiol and the timing of neuroendocrine puberty.
妊娠中期的睾丸类固醇可使绵羊体内控制GnRH分泌的类固醇反馈机制发生性别分化。迄今为止,由于外源性雌激素会干扰母体子宫功能,因此难以研究雌激素代谢产物在神经内分泌功能编程中的作用。我们开发了一种通过联合给予睾酮(T)和雄激素受体拮抗剂氟他胺来研究雌激素产前作用的方法,并检验了以下假设:产前雄激素可对GnRH分泌的雌二醇抑制性反馈控制进行编程,从而使LH青春期增加的时间女性化(提前)。怀孕的绵羊在妊娠第30至90天未接受治疗或接受T、双氢睾酮(DHT)(一种不可芳香化的雄激素)或T加氟他胺治疗。为了研究出生后对类固醇负反馈的反应,对羔羊进行性腺切除并补充雌二醇,并每周两次采集血样监测LH浓度。尽管T和DHT使雌性出现阴茎和阴囊发育,但无论遗传性别如何,T加氟他胺后代的外生殖器在表型上仍为雌性。未接受治疗的雌性以及接受T加氟他胺治疗的雌性和雄性分别在26.4±0.5、26.0±0.7和22.4±1.6周龄时出现循环LH的青春期增加。在暴露于产前雄激素的雌性中,LH增加提前(T:12.0±2.6周;DHT:15.0±2.6周)。这些结果证明了联合使用T和抗雄激素治疗作为增加产前雌二醇暴露的一种方法的有效性。重要的是,这些发现支持了我们的假设,即产前雄激素可对雌二醇的负反馈作用敏感性以及神经内分泌青春期的时间进行编程。