Manji H K, Chen G, Bitran J A, Gusovsky F, Potter W Z
Section on Clinical Pharmacology, National Institute of Mental Health, Bethesda, MD 20892.
Eur J Pharmacol. 1992 Nov 2;227(3):275-82. doi: 10.1016/0922-4106(92)90005-g.
Incubation of the C6 cells with 10 microM idazoxan (an alpha 2-adrenoceptor antagonist and putative antidepressant) for 5 days in vitro resulted in a 23% reduction of beta-adrenoceptor number and a 37% decrease in isoproterenol-induced cyclic AMP accumulation. In contrast, post-receptor stimulated cyclic AMP accumulation (by the use of forskolin or cholera toxin) was unaffected. The desensitization of the beta-adrenoceptor was accompanied by an increase in the KL/KH ratio for this receptor. Chronic in vitro treatment of C6 glioma cells with idazoxan did not significantly affect cholera or pertussis toxin catalyzed ribosylation of Gs and Gi/Go in these cells. Similarly, idazoxan did not alter either the basal levels of protein kinase C (PKC) alpha, or its cytoplasm to membrane translocation. These results suggest that idazoxan may have direct postsynaptic effects, the site of which may be at the level of receptor/G protein interaction.
在体外将C6细胞与10微摩尔的咪唑克生(一种α2肾上腺素能受体拮抗剂及假定的抗抑郁药)孵育5天,导致β肾上腺素能受体数量减少23%,异丙肾上腺素诱导的环磷酸腺苷(cAMP)积累减少37%。相比之下,受体后刺激的cAMP积累(通过使用福斯高林或霍乱毒素)未受影响。β肾上腺素能受体的脱敏伴随着该受体的KL/KH比值增加。用咪唑克生对C6胶质瘤细胞进行慢性体外处理,对这些细胞中霍乱毒素或百日咳毒素催化的Gs和Gi/Go的核糖基化没有显著影响。同样,咪唑克生既未改变蛋白激酶C(PKC)α的基础水平,也未改变其从细胞质到细胞膜的转位。这些结果表明,咪唑克生可能具有直接的突触后效应,其作用位点可能在受体/G蛋白相互作用水平。