Sukul N C, Klemm W R
Department of Veterinary Anatomy, Texas A & M University, College Station 77843.
Arch Int Pharmacodyn Ther. 1988 Sep-Oct;295:40-51.
A few drugs affecting the dopaminergic system were tested for cataleptic effects in mice, and compared with an orally administered plant extract, Agaricus Muscarius 30. Haloperidol, Agaricus, and a low dose of apomorphine (0.3 mg/kg) were cataleptic. Paralleling previously reported results with haloperidol, the Agaricus catalepsy was potentiated by the mixed agonist, apomorphine (5 mg/kg), and by the selective D2 agonist, bromocriptine (5 mg/kg) and was reversed by the D1 agonist, SKF 38393. Naloxone also reversed Agaricus catalepsy, suggesting an involvement of opiate as well as dopaminergic mechanisms. All conditions that produced catalepsy also suppressed spontaneous locomotion, except for Agaricus 30 given alone. These experiments also compared cataleptic drugs by the published "pinch" method that involves repeated trials with a new single-trial method. Catalepsy was produced by the same drugs in both tests, but the single-trial method was more sensitive for disclosing the catalepsy induced by weaker cataleptogens.
测试了几种影响多巴胺能系统的药物对小鼠的僵住效应,并与口服的植物提取物毒蝇伞30进行了比较。氟哌啶醇、毒蝇伞和低剂量的阿扑吗啡(0.3毫克/千克)可引起僵住。与先前报道的氟哌啶醇结果相似,混合激动剂阿扑吗啡(5毫克/千克)、选择性D2激动剂溴隐亭(5毫克/千克)可增强毒蝇伞引起的僵住,而D1激动剂SKF 38393可使其逆转。纳洛酮也可逆转毒蝇伞引起的僵住,提示阿片类以及多巴胺能机制均参与其中。除单独给予毒蝇伞30外,所有引起僵住的情况也都抑制了自发运动。这些实验还通过已发表的“捏压”方法以及一种新的单次试验方法对引起僵住的药物进行了比较。两种试验中相同的药物均可引起僵住,但单次试验方法对于揭示较弱致僵剂诱导的僵住更为敏感。