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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >The serotonin 5-HT(2A) receptor subtype does not mediate apomorphine-induced aggressive behaviour in male Wistar rats.
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The serotonin 5-HT(2A) receptor subtype does not mediate apomorphine-induced aggressive behaviour in male Wistar rats.

机译:5-羟色胺5-HT(2A)受体亚型不介导阿扑吗啡诱导的雄性Wistar大鼠攻击行为。

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摘要

We have studied the effect of the 5-HT(2A) receptor antagonists on apomorphine-induced aggressive behaviour in male Wistar rats. In acute behavioural experiments with apomorphine-pretreated (1.0 mg/kg, s.c., once daily, 2 weeks) animals, risperidone (0.5 and 1.0 mg/kg) inhibited aggressive behaviour, but ketanserin and ritanserin (0.5-5. 0 mg/kg) had no effect on the latency and intensity of aggressive behaviour. Concomitant risperidone (0.5 mg/kg) and haloperidol (0.03 and 0.3 mg/kg) administration blocked aggressive behaviour completely. In conclusion, our experiments confirm that inhibition of the apomorphine-induced aggressive behaviour is elicited by drugs with dopamine (DA) but not with 5-HT(2A) antagonistic activity. Moreover, it may be concluded that the serotonin 5-HT(2A) receptor subtype does not alter the DA-mediated behaviour.
机译:我们已经研究了5-HT(2A)受体拮抗剂对阿扑吗啡诱导的雄性Wistar大鼠攻击行为的影响。在用阿扑吗啡预处理(1.0 mg / kg,皮下注射,每天一次,2周)的动物的急性行为实验中,利培酮(0.5和1.0 mg / kg)抑制侵略性行为,但酮色林和利坦色林(0.5-5。0 mg / kg) )对攻击行为的潜伏时间和强度没有影响。利培酮(0.5 mg / kg)和氟哌啶醇(0.03和0.3 mg / kg)的同时给药完全阻断了攻击行为。总之,我们的实验证实,具有多巴胺(DA)而非5-HT(2A)拮抗活性的药物会引起对阿扑吗啡诱导的攻击行为的抑制。此外,可以得出结论,血清素5-HT(2A)受体亚型不会改变DA介导的行为。

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