Abou Y Z, Farjo I B
Br J Pharmacol. 1979 Feb;65(2):303-9. doi: 10.1111/j.1476-5381.1979.tb07831.x.
1 The behavioural effects induced by histidine were studied in two species. In rabbits, sedation was assessed by the presence of blepharospasm, loss of righting reflex, and loss of response to painful stimuli. In mice, sedation and arousal were assessed by changes in the locomotor activity, exploratory activity, and minimal electroshock seizure threshold.2 The administration of histidine to normal rabbits or mice, in doses of 800 mg/kg and 1000 mg/kg respectively, had no apparent effect on behaviour. Moreover, it did not affect the behavioural excitation induced by L-DOPA (100 mg/kg i.v. in rabbits and 750 mg/kg i.p. in mice) in these animals.3 The administration of histidine with or after L-DOPA in reserpine-treated rabbits (2.5 mg/kg i.v.) or mice (5 mg/kg, i.p.) produced sedation. This sedative effect was dose-dependent.4 The sedative effects induced by histidine after DOPA-induced arousal in reserpine-treated rabbits and mice were prevented by prior injection of the histamine H(1)-receptor blockers, chlorpheniramine (2.5 mg/kg) or diphenhydramine (5 mg/kg).5 Imipramine (7 to 10 mg/kg, i.v.)-induced arousal in reserpine-treated rabbits was also reversed by histidine infusion.6 The infusion of 5-hydroxytryptophan (100 mg/kg, i.v.) with L-DOPA, or of arginine (450 mg/kg, i.v.) with or after L-DOPA, or of histamine (100 mug/kg), i.v.) after L-DOPA, did not affect the DOPA-induced arousal in reserpine-treated rabbits.7 These findings indicate that histamine, formed centrally from exogenous histidine, and released in increased amounts at the synapses in reserpine-treated animals, possesses a central sedative effect. This effect may be sufficient to antagonize the behavioural excitation induced by high levels of catecholamines in the brain of these animals when aroused by L-DOPA administration.8 It is concluded that in addition to the other monoamines, histamine may also be implicated in the regulation of brain excitability.
1 在两个物种中研究了组氨酸诱导的行为效应。在兔子中,通过睑痉挛、翻正反射丧失和对疼痛刺激反应丧失来评估镇静作用。在小鼠中,通过运动活动、探索活动和最小电休克惊厥阈值的变化来评估镇静和觉醒。
2 分别以800mg/kg和1000mg/kg的剂量给正常兔子或小鼠施用组氨酸,对行为没有明显影响。此外,它不影响这些动物中由左旋多巴(兔子静脉注射100mg/kg,小鼠腹腔注射750mg/kg)诱导的行为兴奋。
3 在利血平处理的兔子(静脉注射2.5mg/kg)或小鼠(腹腔注射5mg/kg)中,在给予左旋多巴时或之后给予组氨酸会产生镇静作用。这种镇静作用是剂量依赖性的。
4 在利血平处理的兔子和小鼠中,在左旋多巴诱导觉醒后,组氨酸诱导的镇静作用可通过预先注射组胺H(1)受体阻滞剂氯苯那敏(2.5mg/kg)或苯海拉明(5mg/kg)来预防。
5 利血平处理的兔子中,丙咪嗪(静脉注射7至10mg/kg)诱导的觉醒也可通过输注组氨酸来逆转。
6 在利血平处理的兔子中,将5-羟色氨酸(静脉注射100mg/kg)与左旋多巴一起输注,或将精氨酸(静脉注射450mg/kg)与左旋多巴一起或之后输注,或将组胺(静脉注射100μg/kg)在左旋多巴之后输注,均不影响左旋多巴诱导的觉醒。
7 这些发现表明,由外源性组氨酸在中枢形成并在利血平处理的动物突触中大量释放的组胺具有中枢镇静作用。当通过施用左旋多巴引起这些动物大脑中高水平儿茶酚胺诱导的行为兴奋时,这种作用可能足以拮抗该兴奋。
8 得出的结论是,除其他单胺外,组胺也可能参与大脑兴奋性的调节。