Division of Pharmacology, Utrecht Institute for Pharmaceutical Sciences and Rudolf Magnus Institute of Neuroscience, Utrecht University, Sorbonnelaan, Utrecht, The Netherlands.
J Sex Med. 2011 Jan;8(1):97-108. doi: 10.1111/j.1743-6109.2010.01961.x.
Serotonin (5-HT) is an important neurotransmitter for sexual behaviors. Heterozygous (+/-) serotonin transporter (SERT) rats and SERT knockout rats (-/-) have serotonergic disturbances with significant elevations of basal extracellular 5-HT levels.
To investigate the putative role of the SERT in male sexual behavior.
After extensive sexual training, the effects of the 5-HT(1A/7) receptor agonist ± 8-OH-DPAT, the 5-HT(1A) receptor antagonist WAY100 635 and a combination of both on sexual behaviors of SERT(-/-) and SERT(+/-) knockout and wildtype (SERT(+/+) ) male Wistar rats were examined.
Male rat sexual behaviors of mounts, intromissions, and ejaculations.
SERT(-/-) had lower basal ejaculation frequencies than SERT(+/-) and SERT(+/+) animals. ± 8-OH-DPAT enhanced sexual performance in all three genotypes to the same extent. WAY100635 dose-dependently inhibited sexual behavior in all three genotypes with significant dose to genotype interactions. WAY100635 exerted the strongest effects in SERT(-/-) animals. The combination of a dose range of ± 8-OH-DPAT and a selected dose of WAY100635 revealed only partial antagonism by ± 8-OH-DPAT of the sexual inhibitory effects of WAY100635.
Absence of the serotonin transporter reduces basal ejaculatory performance in male rats. Pharmacological experiments suggest that separate pools of 5-HT(1A) receptors regulate different aspects of sexual performance in male rats. 5-HT(7) receptors may play a minor role in the partial recovery of sexual behavior after combination of ± 8-OH-DPAT and WAY100635. The SERT(-/-) rat may be a model for chronic SSRI treatment, delayed ejaculation, anorgasmia, and/or low libido.
血清素(5-HT)是性行为的重要神经递质。杂合子(+/-)血清素转运体(SERT)大鼠和 SERT 敲除大鼠(-/-)具有明显升高的基础细胞外 5-HT 水平的血清素能障碍。
研究 SERT 在雄性性行为中的可能作用。
经过广泛的性训练,研究了 5-HT(1A/7)受体激动剂±8-OH-DPAT、5-HT(1A)受体拮抗剂 WAY100635 及其组合对 SERT(-/-)和 SERT(+/-)敲除和野生型(SERT(+/+))雄性 Wistar 大鼠性行为的影响。
雄性大鼠的交配、插入和射精次数。
SERT(-/-)的基础射精频率低于 SERT(+/-)和 SERT(+/+)动物。±8-OH-DPAT 以相同的程度增强了所有三种基因型的性表现。WAY100635 剂量依赖性地抑制了所有三种基因型的性行为,且具有显著的剂量-基因型相互作用。WAY100635 在 SERT(-/-)动物中产生最强的作用。±8-OH-DPAT 和选定剂量的 WAY100635 的剂量范围组合仅部分拮抗 WAY100635 对性抑制作用。
缺乏血清素转运体可降低雄性大鼠的基础射精性能。药理实验表明,5-HT(1A)受体的不同池调节雄性大鼠不同方面的性表现。5-HT(7)受体可能在±8-OH-DPAT 和 WAY100635 组合后部分恢复性行为中起次要作用。SERT(-/-)大鼠可能是慢性 SSRI 治疗、延迟射精、不射精症和/或低性欲的模型。