Massi P, Rubino T, Parenti M, Giagnoni G, Groppetti A, Parolaro D
Institute of Pharmacology, Faculty of Sciences, University of Milan, Italy.
Eur J Pharmacol. 1993 Oct 12;243(1):65-71. doi: 10.1016/0014-2999(93)90168-h.
We studied the effect of intracerebroventricular pretreatment with pertussis toxin and cholera toxin on morphine catalepsy in rats. Pertussis toxin (1 micrograms/rat, two, three and six days before) did not affect catalepsy evoked by central morphine. Cholera toxin (1 micrograms/rat) did not affect morphine catalepsy after 24 h and 48 h, but significantly reduced it (about 60%) after three and five days. Ten days later the morphine response had totally recovered. This effect was selective, since morphine analgesia was not modified. The reduction of catalepsy appeared unrelated to the ability of cholera toxin to raise cAMP levels, as demonstrated by the different time course of changes in striatal cholera toxin-stimulated adenylate cyclase activity. The effect required an intact cholera toxin molecule and did not occur with a similar dose of cholera toxin-B subunit. These findings demonstrate that catalepsy is an opioid effect not linked to pertussis toxin-sensitive G proteins and suggest that the Gs protein might be involved.
我们研究了脑室注射百日咳毒素和霍乱毒素预处理对大鼠吗啡诱导的僵住症的影响。百日咳毒素(1微克/只大鼠,在注射吗啡前2天、3天和6天注射)不影响中枢注射吗啡诱发的僵住症。霍乱毒素(1微克/只大鼠)在注射后24小时和48小时不影响吗啡诱导的僵住症,但在注射后3天和5天显著降低僵住症(约60%)。10天后,对吗啡的反应完全恢复。这种作用具有选择性,因为吗啡镇痛作用未改变。僵住症的减轻似乎与霍乱毒素升高cAMP水平的能力无关,这一点通过纹状体中霍乱毒素刺激的腺苷酸环化酶活性变化的不同时间进程得以证明。这种作用需要完整的霍乱毒素分子,相似剂量的霍乱毒素B亚基则不会产生此作用。这些发现表明,僵住症是一种与百日咳毒素敏感的G蛋白无关的阿片类效应,并提示Gs蛋白可能参与其中。