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血清素转运体缺失突变与雌性大鼠的性行为:5-HT1A 受体脱敏。

Serotonin transporter null mutation and sexual behavior in female rats: 5-HT1A receptor desensitization.

机构信息

Department of Psychopharmacology, Utrecht Institute for Pharmaceutical Sciences and Rudolf Magnus Institute of Neuroscience, Utrecht University, Utrecht, The Netherlands.

出版信息

J Sex Med. 2010 Jul;7(7):2424-34. doi: 10.1111/j.1743-6109.2010.01829.x. Epub 2010 Apr 26.

Abstract

INTRODUCTION

Serotonin plays a key role in sexual behavior. In serotonin transporter (SERT) knockout rats (-/-), basal extracellular 5-HT levels are considerably increased, indicating a serotonergic disturbance. Heterozygous SERT(+/-) rats express 50% of SERT in comparison to wild-type rats and may therefore model the s/s phenotype of the human SERT promoter (5-HTTLPR) polymorphism.

AIM

In the present study, we used both homozygote and heterozygote SERT knockout and wild-type rats (+/+) to study the putative role of the SERT in female sexual behavior.

METHODS

Female rats were brought into estrous by hormonal injections before a paced mating sex test. The effects of the 5-HT(1A)/5-HT(7) receptor agonist (+/-)-8-hydroxy-2-(dipropylamino)tetralin hydrobromide (+/-8-OH-DPAT) (0.03-1 mg/kg s.c.) and the 5-HT(1A) receptor antagonist WAY-100635 (0.1-1-mg/kg i.p.) on sexual behaviors of the females were tested separately and in a selected combination of both in all three genotypes.

MAIN OUTCOME MEASURES

Proceptive (darting and hopping) and receptive (lordosis) behaviors were quantified.

RESULTS

Basal proceptive and receptive sexual activities were not different between SERT+/+, +/- and -/- female rats. The dose-effect curve after +/-8-OH-DPAT for these activities was clearly shifted to the right in SERT-/- animals compared to other genotypes. WAY-100635 alone had no effect on sexual behavior in any genotype, but was able to antagonize the +/-8-OH-DPAT-induced decrease in sexual activities indicating the involvement of the 5-HT(1A) receptor.

CONCLUSIONS

The absence (-/-) or reduced (+/-) expression of SERT does not affect basal sexual activity in female rats in a paced mating situation. The data indicate a desensitized 5-HT1A receptor in the SERT-/-, but not in the SERT+/- females. Under normal basal conditions, desensitized 5-HT1A receptors apparently do not play a role in female sexual behavior of the SERT-/-. However, upon activation of the 5-HT1A receptor in "normal" females (SERT+/+ and SERT+/-), a hyposexual behavior is induced.

摘要

简介

血清素在性行为中起着关键作用。在 5-羟色胺转运体(SERT)敲除大鼠(-/-)中,细胞外 5-HT 水平显著升高,表明存在血清素能障碍。杂合子 SERT(+/-)大鼠的 SERT 表达量为野生型大鼠的 50%,因此可能模拟人类 SERT 启动子(5-HTTLPR)多态性的 s/s 表型。

目的

本研究使用纯合子和杂合子 SERT 敲除大鼠以及野生型大鼠(+/+)来研究 SERT 在雌性性行为中的潜在作用。

方法

雌性大鼠通过激素注射进入发情期,然后进行定时交配性测试。单独测试 5-HT1A/5-HT7 受体激动剂 (+/-)-8-羟基-2-(二丙基氨基)四氢萘盐酸盐(+/-8-OH-DPAT)(0.03-1mg/kg sc)和 5-HT1A 受体拮抗剂 WAY-100635(0.1-1mg/kg ip)对雌性性行为的影响,并在所有三种基因型中分别测试这两种药物的组合对性行为的影响。

主要观察指标

探究性行为(扑向和跳跃)和接受性行为(背侧卧位)。

结果

SERT+/+、+/-和-/-雌性大鼠的基础探究和接受性行为没有差异。与其他基因型相比,SERT-/-动物的 +/-8-OH-DPAT 剂量-效应曲线明显右移。WAY-100635 单独使用对任何基因型的性行为均无影响,但能拮抗 +/-8-OH-DPAT 诱导的性行为下降,表明 5-HT1A 受体参与其中。

结论

SERT 缺失(-/-)或表达减少(+/-)不会影响 paced mating 情况下雌性大鼠的基础性行为。数据表明 SERT-/-大鼠的 5-HT1A 受体脱敏,但 SERT+/-大鼠则不然。在正常基础条件下,脱敏的 5-HT1A 受体显然在 SERT-/-雌性大鼠的性行为中不起作用。然而,在“正常”雌性大鼠(SERT+/+和 SERT+/-)中激活 5-HT1A 受体时,会诱导低性欲行为。

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