Moritoki H, Fukuda H, Kanaya J, Ishida Y
J Pharm Pharmacol. 1986 Oct;38(10):737-41. doi: 10.1111/j.2042-7158.1986.tb04481.x.
5-Hydroxytryptamine (5-HT) slightly inhibited the twitch contractions of rat vas deferens caused by single pulse field stimulation at 0.1 Hz. The inhibitory effect of 5-HT was much less in the epididymal portion than in the prostatic portion of the vas deferens. Ketanserin potentiated the prejunctional inhibitory effect of 5-HT and attenuated its stimulatory effect. This potentiation was observable only in the epididymal portion, of the vas deferens. Cyproheptadine and mianserin, but not methysergide, had essentially similar potentiating effects to those of ketanserin. These results suggest that the 5-HT receptor that mediates prejunctional inhibition is not of the 5-HT2 type, and that ketanserin acts by suppressing the 5-HT-induced stimulatory effect, which is possibly mediated by a postjunctional 5-HT2 receptor, thus unmasking the inhibitory effect of 5-HT.
5-羟色胺(5-HT)对0.1Hz单脉冲场刺激引起的大鼠输精管抽搐收缩有轻微抑制作用。5-HT在输精管附睾段的抑制作用远小于前列腺段。酮色林增强了5-HT的突触前抑制作用,并减弱了其刺激作用。这种增强作用仅在输精管附睾段可见。赛庚啶和米安色林,但不是麦角新碱,对酮色林有基本相似的增强作用。这些结果表明,介导突触前抑制的5-HT受体不是5-HT2型,酮色林通过抑制5-HT诱导的刺激作用发挥作用,这种刺激作用可能由突触后5-HT2受体介导,从而揭示了5-HT的抑制作用。