Pagnini G, Camanni F, Crispino A, Portaleone P
J Pharm Pharmacol. 1978 Feb;30(2):92-5. doi: 10.1111/j.2042-7158.1978.tb13169.x.
The activity of 2-bromo-alpha-ergokryptine (bromocriptine) (5 mg kg-1, i.p.) on adenylate cyclase and on phosphodiesterase (PDE-PDE II) of rat striatum, has been examined both in vitro and in vivo. In vitro and in vivo bromocriptine stimulated adenylate cyclase activity, but reduced the stimulating effect of dopamine on adenylate cyclase activity. Bromocriptine showed a dose-dependent biphasic action on phosphodiesterases in vitro while in vivo it stimulated them. The results obtained proved bromocriptine to have an agonist-antagonist action at striatal dopamine receptor level, with a relevant effect on the cAMP system.
已在体外和体内研究了2-溴-α-麦角隐亭(溴隐亭)(5毫克/千克,腹腔注射)对大鼠纹状体腺苷酸环化酶和磷酸二酯酶(PDE - PDE II)的作用。在体外和体内,溴隐亭均刺激腺苷酸环化酶活性,但降低了多巴胺对腺苷酸环化酶活性的刺激作用。溴隐亭在体外对磷酸二酯酶表现出剂量依赖性双相作用,而在体内则刺激它们。所获得的结果证明溴隐亭在纹状体多巴胺受体水平具有激动剂 - 拮抗剂作用,对环磷酸腺苷(cAMP)系统有显著影响。