首页> 外文期刊>The journal of sexual medicine >Serotonin transporter null mutation and sexual behavior in female rats: 5-HT1A receptor desensitization.
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Serotonin transporter null mutation and sexual behavior in female rats: 5-HT1A receptor desensitization.

机译:5-羟色胺转运蛋白无效突变和雌性大鼠的性行为:5-HT1A受体脱敏。

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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.
机译:简介:5-羟色胺在性行为中起关键作用。在血清素转运蛋白(SERT)剔除大鼠(-/-)中,基础细胞外5-HT水平显着增加,表明血清素能紊乱。与野生型大鼠相比,杂合型SERT(+/-)大鼠表达50%的SERT,因此可以模拟人SERT启动子(5-HTTLPR)多态性的s / s表型。目的:在本研究中,我们使用纯合子和杂合子SERT基因敲除和野生型大鼠(+ / +)研究SERT在女性性行为中的假定作用。方法:在进行有规律的交配性试验之前,通过激素注射使雌性大鼠发情。 5-HT(1A)/ 5-HT(7)受体激动剂(+/-)-8-羟基-2-(二丙基氨基)四氢呋喃氢溴酸盐(+/- 8-OH-DPAT)的作用(0.03-1 mg / kg sc)和5-HT(1A)受体拮抗剂WAY-100635(0.1-1-mg / kg ip ip)对雌性的性行为进行了单独测试,并以这三种基因型的两种选择组合进行了测试。主要观察指标:量化感受性(飞跃和跳跃)和感受性(罗氏病)行为。结果:雌性大鼠在SERT + / +,+ /-和-/-的基础性行为和接受性行为均无差异。与其他基因型相比,+ /-8-OH-DPAT处理后这些活动的剂量效应曲线在SERT-/-动物中明显向右移动。单独的WAY-100635对任何基因型的性行为都没有影响,但是能够拮抗+/- 8-OH-DPAT诱导的性活动减少,表明参与了5-HT(1A)受体。结论:在有节律的交配情况下,SERT的缺乏(-/-)或减少(+/-)的表达不会影响雌性大鼠的基础性活动。数据表明在SERT-/-中有脱敏的5-HT1A受体,但在SERT +/-雌性中没有。在正常的基础条件下,脱敏的5-HT1A受体显然在SERT-/-的女性性行为中不起作用。但是,在“正常”女性(SERT + / +和SERT +/-)中激活5-HT1A受体后,会诱发性欲低下的行为。

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