Mulner O, Tso J, Huchon D, Ozon R
Cell Differ. 1983 Apr;12(4):211-8. doi: 10.1016/0045-6039(83)90030-1.
Progesterone decreases the cAMP level of Xenopus oocytes which had been pretreated with cholera toxin (6 nM) and IBMX (1 mM); its action is obtained either by exposure to external hormone (1 micro M) or by microinjection of 50 nl of a 1 mM progesterone solution in paraffin oil. The cAMP content can be decreased in hormone-free oocytes by the calcium ionophore A 23187 or by microinjection of calcium-calmodulin. Conversely when endogenous calcium-calmodulin is inhibited by microinjection of either anticalmodulin antibodies or fluphenazine the cAMP content is increased. In all experimental conditions (high or low levels of intracellular calmodulin), progesterone is always capable of decreasing the oocyte cAMP concentration. Our results favor the view that the cAMP content is negatively controlled, probably via an inhibition of the adenylate cyclase activity, by two parallel mechanisms: the first involves calmodulin, the second results in an action of progesterone which does not require the intermediary formation of the calcium-calmodulin complex.
孕酮可降低经霍乱毒素(6 nM)和异丁基甲基黄嘌呤(IBMX,1 mM)预处理的非洲爪蟾卵母细胞的环磷酸腺苷(cAMP)水平;其作用可通过暴露于外源激素(1 μM)或显微注射50 nl石蜡油中的1 mM孕酮溶液来实现。钙离子载体A 23187或显微注射钙调蛋白可使无激素卵母细胞中的cAMP含量降低。相反,当通过显微注射抗钙调蛋白抗体或氟奋乃静抑制内源性钙调蛋白时,cAMP含量会增加。在所有实验条件下(细胞内钙调蛋白水平高或低),孕酮始终能够降低卵母细胞的cAMP浓度。我们的结果支持这样一种观点,即cAMP含量受到负调控,可能是通过两种平行机制抑制腺苷酸环化酶活性实现的:第一种机制涉及钙调蛋白,第二种机制是孕酮的作用,该作用不需要钙调蛋白复合物的中间形成。