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5α-雄甾烷-3β,17β-二醇(3β-二醇)是5α-二氢睾酮的一种雌激素代谢产物,是成年大鼠腹侧前列腺中雌激素受体ERβ表达的有效调节剂。

5alpha-Androstane-3beta,17beta-diol (3beta-diol), an estrogenic metabolite of 5alpha-dihydrotestosterone, is a potent modulator of estrogen receptor ERbeta expression in the ventral prostrate of adult rats.

作者信息

Oliveira André G, Coelho Polyanna H, Guedes Fernanda D, Mahecha Germán A B, Hess Rex A, Oliveira Cleida A

机构信息

Department of Morphology, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.

出版信息

Steroids. 2007 Dec;72(14):914-22. doi: 10.1016/j.steroids.2007.08.001. Epub 2007 Aug 9.

Abstract

Prostate is one of the major targets for dihydrotestosterone (DHT), however this gland is also recognized as a nonclassical target for estrogen as it expresses both types of estrogen receptors (ER), especially ERbeta. Nevertheless, the concentrations of aromatase and estradiol in the prostate are low, indicating that estradiol may not be the only estrogenic molecule to play a role in the prostate. It is known that DHT can be metabolized to 5alpha-androstane-3beta,17beta-diol (3beta-diol), a hormone that binds to ERbeta but not to AR. The concentration of 3beta-diol in prostate is much higher than that of estradiol. Based on the high concentration of 3beta-diol and since this metabolite is a physiological ERbeta ligand, we hypothesized that 3beta-diol would be involved in the regulation of ERbeta expression. To test this hypothesis, adult male rats were submitted to castration followed by estradiol, DHT or 3beta-diol replacement. ERbeta and AR protein levels in the prostate were investigated by immunohistochemistry and Western blotting assays. The results showed that after castration, the structure of the prostate was dramatically changed and ERbeta and AR protein levels were decreased. Estradiol had just minor effects on the parameters analyzed. DHT-induced partial recovery of ERbeta while it was the most effective inductor of AR expression. Replacement with 3beta-diol-induced the highest levels of ERbeta, but was comparatively less effective in recovering the AR expression and the gland structure. These results offer evidence that one functional role of 3beta-diol in the prostate may be autoregulation of its natural receptor, ERbeta.

摘要

前列腺是双氢睾酮(DHT)的主要作用靶点之一,然而该腺体也被认为是雌激素的非经典作用靶点,因为它表达两种类型的雌激素受体(ER),尤其是ERβ。尽管如此,前列腺中芳香化酶和雌二醇的浓度较低,这表明雌二醇可能不是唯一在前列腺中发挥作用的雌激素分子。已知DHT可代谢为5α-雄烷-3β,17β-二醇(3β-二醇),一种与ERβ结合但不与雄激素受体(AR)结合的激素。前列腺中3β-二醇的浓度远高于雌二醇。基于3β-二醇的高浓度以及该代谢产物是一种生理性ERβ配体,我们推测3β-二醇会参与ERβ表达的调节。为了验证这一假设,对成年雄性大鼠进行去势手术,随后给予雌二醇、DHT或3β-二醇替代治疗。通过免疫组织化学和蛋白质印迹分析研究前列腺中ERβ和AR蛋白水平。结果显示,去势后,前列腺结构发生显著变化,ERβ和AR蛋白水平降低。雌二醇对所分析的参数影响较小。DHT诱导ERβ部分恢复,而它是AR表达最有效的诱导剂。用3β-二醇替代诱导出最高水平的ERβ,但在恢复AR表达和腺体结构方面相对效果较差。这些结果提供了证据,表明3β-二醇在前列腺中的一个功能作用可能是对其天然受体ERβ的自动调节。

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