Green A R, O'Shaughnessy K, Hammond M, Schächter M, Grahame-Smith D G
Neuropharmacology. 1983 May;22(5):573-8. doi: 10.1016/0028-3908(83)90147-8.
The effect of pirenperone, a putative 5-HT2 receptor antagonist, on various 5-HT-mediated behavioural responses has been examined. The head twitch response in mice, induced by administration of carbidopa (25 mg/kg) followed by 5-hydroxytryptophan (5-HTP) (200 mg/kg), was inhibited in a dose-dependent manner by pirenperone, with an ED50 of 76 micrograms/kg. The appearance of head weaving, forepaw treading and hind-limb abduction, which followed the administration of tranylcypromine (5 mg/kg) plus L-tryptophan (100 mg/kg) or quipazine (50 mg/kg) to rats, was also inhibited by pretreatment with pirenperone (100 micrograms/kg). Pirenperone did not alter the rate of 5-HT synthesis in the rat brain. Whilst pirenperone (100 micrograms/kg) did decrease methamphetamine-induced locomotor activity in rats, a dose of haloperidol producing a similar inhibition of this response did not alter the 5-HT-mediated behaviour. It is suggested, therefore, that the currently used 5-HT-induced behavioural models are 5-HT2 receptor-mediated.
已对一种假定的5-羟色胺2(5-HT2)受体拮抗剂匹伦哌隆对各种5-羟色胺介导的行为反应的影响进行了研究。在小鼠中,先给予卡比多巴(25毫克/千克),随后给予5-羟色氨酸(5-HTP)(200毫克/千克)所诱导的头部抽搐反应,被匹伦哌隆以剂量依赖性方式抑制,半数有效剂量(ED50)为76微克/千克。给大鼠服用反苯环丙胺(5毫克/千克)加L-色氨酸(100毫克/千克)或喹哌嗪(50毫克/千克)后出现的头部摆动、前爪踩踏和后肢外展,也被匹伦哌隆(100微克/千克)预处理所抑制。匹伦哌隆未改变大鼠脑中5-羟色胺的合成速率。虽然匹伦哌隆(100微克/千克)确实降低了大鼠中甲基苯丙胺诱导的运动活性,但产生类似这种反应抑制作用的氟哌啶醇剂量并未改变5-羟色胺介导的行为。因此,有人提出,目前使用的5-羟色胺诱导行为模型是由5-HT2受体介导的。