Department of Psychopharmacology, Utrecht Institute for Pharmaceutical Sciences and Rudolf Magnus Institute of Neuroscience, Utrecht University, Utrecht, The Netherlands.
J Sex Med. 2010 Jul;7(7):2424-34. doi: 10.1111/j.1743-6109.2010.01829.x. Epub 2010 Apr 26.
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.
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.
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.
Proceptive (darting and hopping) and receptive (lordosis) behaviors were quantified.
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.
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.
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。
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。
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。
探究性行为(扑向和跳跃)和接受性行为(背侧卧位)。
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。
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。