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神经甾体 7α-羟基孕烯醇酮参与了雄性中国石龙子的求偶行为。

Involvement of the neurosteroid 7α-hydroxypregnenolone in the courtship behavior of the male newt Cynops pyrrhogaster.

机构信息

Physiology Department-I, Nara Medical University, Nara 634-8521, Japan.

出版信息

Horm Behav. 2012 Sep;62(4):375-80. doi: 10.1016/j.yhbeh.2012.07.001. Epub 2012 Jul 13.

Abstract

Reproductive behavior in amphibians, as in other vertebrate animals, is controlled by multiple hormones. A neurosteroid, 7α-hydroxypregnenolone, has recently been found to enhance locomotor activity in the male newt, Cynops pyrrhogaster. Here, we show that this neurosteroid is also involved in enhancing the expression of courtship behavior. Intracerebroventricular (ICV) injection of 7α-hydroxypregnenolone enhanced courtship behavior dose-dependently in the sexually undeveloped males that had been pretreated with prolactin and gonadotropin, which is known to bring the males to a sexually developed state. But, unlike the case in the locomotion activity, 7α-hydroxypregnenolone did not elicit the behavior in males receiving no prior injections of these hormones. ICV administration of ketoconazole, an inhibitor of the steroidogenic enzyme cytochrome P450s, suppressed the spontaneously occurring courtship behavior in sexually active males. Supplementation with 7α-hydroxypregnenolone reversed the effect of ketoconazole in these animals. It was also demonstrated that the effect of the neurosteroid on the courtship behavior was blocked by a dopamine D2-like, but not by a D1-like, receptor antagonist. These results indicate that endogenous 7α-hydroxypregnenolone enhances the expression of the male courtship behavior through a dopaminergic system mediated by a D2-like receptor in the brain.

摘要

两栖动物的繁殖行为与其他脊椎动物一样,受多种激素控制。一种神经甾体,7α-羟孕烯醇酮,最近被发现可增强雄性蝾螈的运动活性。在这里,我们表明这种神经甾体也参与增强求偶行为的表达。脑室内(ICV)注射 7α-羟孕烯醇酮可剂量依赖性地增强已用催乳素和促性腺激素预处理的未发育雄性的求偶行为,已知这些激素可使雄性进入性发育状态。但是,与运动活性的情况不同,7α-羟孕烯醇酮不会引起未接受这些激素预先注射的雄性产生行为。ICV 给予酮康唑,一种类固醇生成酶细胞色素 P450s 的抑制剂,可抑制性活跃雄性自发发生的求偶行为。用 7α-羟孕烯醇酮补充可逆转这些动物中酮康唑的作用。还表明,神经甾体对求偶行为的作用被多巴胺 D2 样,但不是 D1 样,受体拮抗剂阻断。这些结果表明,内源性 7α-羟孕烯醇酮通过大脑中的 D2 样受体介导的多巴胺能系统增强雄性求偶行为的表达。

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