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雌激素 G 蛋白偶联受体 30(GPR30)和性经验在雄性大鼠性激励动机中的作用。

The role of estrogen G-protein coupled receptor 30 (GPR30) and sexual experience in sexual incentive motivation in male rats.

机构信息

Edinboro University of Pennsylvania, Department of Psychology, United States; Franklin and Marshall College, Department of Psychology, United States.

Edinboro University of Pennsylvania, Department of Psychology, United States.

出版信息

Physiol Behav. 2017 Aug 1;177:176-181. doi: 10.1016/j.physbeh.2017.05.001. Epub 2017 May 1.

Abstract

Male rats exhibit reductions in sexual motivation following systemic administration of drugs that inhibit the conversion of testosterone to estrogen, which indicates that estrogen signaling plays a role in male rat sexual motivation. Given that estrogen G-protein coupled receptor 30 (GPR30) is expressed in brain areas that are important for male sexual behaviors and endocrine function, the primary aim of the current study was to examine the role that GPR30 plays in sexual motivation in both sexually naïve and sexually experienced male rats. Following the final treatment with either a GPR30 antagonist (G-15) or vehicle control, male rats were placed into the center chamber of a larger three-chambered testing arena that was designed to assess sexual incentive motivation. A sexually receptive stimulus female rat and a stimulus male rat were individually confined to one of the two smaller chambers that were each separated by a perforated partition from the larger end chambers, which test rats had access to. Relative to vehicle treated rats, male rats treated with G-15 exhibited a reduction in the percentage of time spent in the vicinity of a sexually receptive female rat. Although G-15 reduced sexual incentive motivation independent of sexual experience, only sexually-naïve rats treated with G-15 did not exhibit a preference for the sexually receptive stimulus female rat. Collectively, these results indicate that interference with estrogen signaling at GPR30 reduces sexual motivation and that the lack of preference for a sexually receptive female rat over a male rat following G-15 treatment is abrogated by previous sexual experience.

摘要

雄性大鼠在系统给予抑制睾酮转化为雌激素的药物后,其性动机降低,这表明雌激素信号在雄性大鼠的性动机中起作用。鉴于雌激素 G 蛋白偶联受体 30(GPR30)在对雄性性行为和内分泌功能很重要的脑区表达,本研究的主要目的是检查 GPR30 在性动机中的作用在性经验丰富和性经验不足的雄性大鼠中。在最后一次用 GPR30 拮抗剂(G-15)或载体对照处理后,雄性大鼠被放置在一个更大的三腔测试场的中心腔室中,该场室旨在评估性激励动机。一只接受性刺激的雌性大鼠和一只刺激雄性大鼠分别被限制在两个较小的腔室之一中,每个腔室都通过穿孔隔板与大鼠可以进入的较大端腔室隔开。与接受载体处理的大鼠相比,用 G-15 处理的雄性大鼠在靠近接受性雌性大鼠的时间百分比减少。尽管 G-15 独立于性经验减少了性激励动机,但只有接受 G-15 处理的性经验不足的大鼠没有表现出对接受性刺激雌性大鼠的偏好。总之,这些结果表明,在 GPR30 处干扰雌激素信号会降低性动机,并且在 G-15 处理后缺乏对接受性雌性大鼠相对于雄性大鼠的偏好被先前的性经验所消除。

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