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5-羟色胺(5-HT)1A和1B受体亚型在雄性小鼠性唤起中的作用

Involvement of the 5-HT(1A) and 5-HT(1B) serotonergic receptor subtypes in sexual arousal in male mice.

作者信息

Popova N K, Amstislavskaya T G

机构信息

Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Pr. Lavrentjeva 10, Novosibirsk, 630090, Russia.

出版信息

Psychoneuroendocrinology. 2002 Jul;27(5):609-18. doi: 10.1016/s0306-4530(01)00097-x.

Abstract

The presence of a sexually receptive female behind a partition that prevents physical contact, but not seeing or smelling, increases blood testosterone level and induces the specific behavior in CBA male mice so that they more frequently approach the partition and spend more time near it in an attempt to make their way to the female. Treatment with the selective 5-HT(1A) serotonin receptor agonist 8-OH-DPAT (0.1, 0.25, 0.5 and 2.0 mg/kg) induced a dose-dependent decrease in the amount of time spent by the males near the partition, or "partition time", which is considered the main pattern of sexual motivation. The activating effect of female exposure on the male's pituitary-testicular system was totally blocked, as no increase in plasma testosterone level was observed. The 5-HT(1A) antagonist p-MPPI (0.1, 0.2 and 0.4 mg/kg) itself did not affect behavior or alter plasma testosterone, but attenuated the inhibiting effect of 8-OH-DPAT on behavior and totally antagonised the effect of the 5-HT(1A) agonist on testosterone response. The 5-HT(1B) agonist CGS-12066A (1.0 and 2.0 mg/kg) has no influence on the plasma testosterone increase exhibited by the male in response to female exposure. At the same time, either dose of CGS-12066A significantly reduced the partition time. The conclusion was made that the 5-HT(1A) subtype is involved in controlling both behavioral and hormonal indices of sexual arousal in male mice, while the 5-HT(1B) receptors antagonise sexual motivation, but do not modify the hypothalamic-pituitary-testicular response.

摘要

在隔板后存在一只处于性接受期的雌性小鼠,隔板虽能防止身体接触,但不影响视觉或嗅觉,这会使CBA雄性小鼠的血液睾酮水平升高,并诱发特定行为,使其更频繁地靠近隔板并在其附近停留更长时间,试图接近雌性。用选择性5-羟色胺(5-HT)(1A)受体激动剂8-羟基二丙胺基四氢萘(8-OH-DPAT)(0.1、0.25、0.5和2.0毫克/千克)进行处理,会导致雄性小鼠在隔板附近停留的时间,即“隔板时间”呈剂量依赖性减少,而“隔板时间”被视为性动机的主要模式。雌性暴露对雄性垂体-睾丸系统的激活作用被完全阻断,因为未观察到血浆睾酮水平升高。5-HT(1A)拮抗剂对氯苯哌嗪(p-MPPI)(0.1、0.2和0.4毫克/千克)本身不影响行为或改变血浆睾酮水平,但可减弱8-OH-DPAT对行为的抑制作用,并完全拮抗5-HT(1A)激动剂对睾酮反应的影响。5-HT(1B)激动剂CGS-12066A(1.0和2.0毫克/千克)对雄性小鼠因雌性暴露而出现的血浆睾酮升高没有影响。与此同时,CGS-12066A的任一剂量均显著缩短了隔板时间。得出的结论是,5-HT(1A)亚型参与控制雄性小鼠性唤起的行为和激素指标,而5-HT(1B)受体拮抗性行为动机,但不改变下丘脑-垂体-睾丸反应。

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