Erzin-Waters C, Muller P, Seeman P
Can J Physiol Pharmacol. 1976 Aug;54(4):516-9. doi: 10.1139/y76-071.
To investigate the extent of cholinergic involvement in opiate-induced catalepsy, the effects of three anticholinergic drugs were studied on morphine-induced catalepsy. Haloperidol-induced catalepsy was also examined. Maximum catalepsy in rats was obtained with 30 mg/kg morphine or 3 mg/kg haloperidol. The anticholinergic drugs atropine, benztropine, and scopolamine were unable to antagonize morphine-induced catalepsy, yet readily antagonized haloperidol-induced catalepsy. Low doses of apomorphine (7.5 mg/kg), on the other hand, readily antagonized morphine catalepsy, but 13-fold higher doses of apomorphine were needed to block haloperidol-induced catalepsy. The results are compatible with the idea that catalepsy can be mediated via the striatum or the amygdala; morphine-dopamine antagonism may occur in the amygdala, whereas morphine-dopamine-cholinergic interactions occur in the striatum.
为研究胆碱能系统在阿片类药物所致僵住症中的作用程度,研究了三种抗胆碱能药物对吗啡所致僵住症的影响。同时也检测了氟哌啶醇所致僵住症。大鼠经30mg/kg吗啡或3mg/kg氟哌啶醇可出现最大程度的僵住症。抗胆碱能药物阿托品、苯海索和东莨菪碱不能拮抗吗啡所致僵住症,但能轻易拮抗氟哌啶醇所致僵住症。另一方面,低剂量的阿扑吗啡(7.5mg/kg)能轻易拮抗吗啡所致僵住症,但需要13倍高剂量的阿扑吗啡才能阻断氟哌啶醇所致僵住症。这些结果与僵住症可通过纹状体或杏仁核介导的观点相符;吗啡-多巴胺拮抗作用可能发生在杏仁核,而吗啡-多巴胺-胆碱能相互作用发生在纹状体。