Lassen J B
Acta Pharmacol Toxicol (Copenh). 1979 Aug;45(2):161-5. doi: 10.1111/j.1600-0773.1979.tb02376.x.
Apomorphine (ap) was administered subcutaneously to mice kept in individual cages. Ap elicited an abnormal vertical climbing behaviour. The muscarinomimetics physostigmine and oxotremorine as well as the neuroleptics clozapine and haloperidol inhibited the climbing produced by ap 1 mg/kg. A small inactive dose of physostigmine potentiated the effect of clozapine but not that of haloperidol. The anticholinergic atropine antagonized the effect of physostigmine, oxotremozine, clozapine and haloperidol. The climbing behaviour produced by ap is presumably due to stimulation of dopamine receptors and this effect can be antagonized either by blockade of dopamine receptors or by activation of muscarinic receptors. Some lines of evidence suggest that the ap-inhibitory effect of clozapine may be partly due to a muscarinomimetic effect.
将阿扑吗啡(ap)皮下注射到单独饲养在笼子里的小鼠体内。阿扑吗啡引发了异常的垂直攀爬行为。毒蕈碱模拟剂毒扁豆碱和氧化震颤素以及抗精神病药物氯氮平和氟哌啶醇抑制了1毫克/千克阿扑吗啡所产生的攀爬行为。小剂量无活性的毒扁豆碱增强了氯氮平的作用,但没有增强氟哌啶醇的作用。抗胆碱能药物阿托品拮抗了毒扁豆碱、氧化震颤素、氯氮平和氟哌啶醇的作用。阿扑吗啡产生的攀爬行为可能是由于多巴胺受体的刺激,这种作用可以通过阻断多巴胺受体或激活毒蕈碱受体来拮抗。一些证据表明,氯氮平对阿扑吗啡的抑制作用可能部分归因于毒蕈碱模拟效应。