Ishikawa S, Saito T
Department of Medicine, Jichi Medical School, Tochigi, Japan.
Biochem Biophys Res Commun. 1990 Jan 15;166(1):411-6. doi: 10.1016/0006-291x(90)91960-z.
The effect of extracellular calcium (Ca2+) on the cellular action of forskolin was studied using a Na+, K(+)-ATPase inhibitor ouabain in rat renal papillary collecting tubule cells in culture. Forskolin-induced cAMP production was enhanced by the pretreatment of cells with ouabain, providing that a dose-dependent curve with forskolin shifted to the left. The enhancement by ouabain of cellular cAMP production in response to forskolin was totally blunted by cotreatment with cobalt, verapamil, or Ca2(+)-free medium containing 1 mM EGTA. In addition, two dissimilar antagonists of calmodulin, namely trifluoperazine and N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide (W - 7), attenuated the ouabain's effect on cAMP production in response to forskolin. These results therefore indicate that ouabain enhances the activation of adenylate cyclase by forskolin, mediated through cellular free Ca2+, in renal papillary collecting tubule cells, and that extracellular Ca2+ is an important source for cellular Ca2+ mobilization by ouabain.
在培养的大鼠肾乳头集合管细胞中,使用钠钾ATP酶抑制剂哇巴因研究细胞外钙(Ca2+)对福斯高林细胞作用的影响。用哇巴因预处理细胞可增强福斯高林诱导的环磷酸腺苷(cAMP)生成,使得福斯高林的剂量依赖性曲线向左移动。与钴、维拉帕米或含1 mM乙二醇双四乙酸(EGTA)的无钙培养基共同处理,可完全消除哇巴因对福斯高林诱导的细胞cAMP生成的增强作用。此外,两种不同的钙调蛋白拮抗剂,即三氟拉嗪和N-(6-氨基己基)-5-氯-1-萘磺酰胺(W - 7),减弱了哇巴因对福斯高林诱导的cAMP生成的作用。因此,这些结果表明,在肾乳头集合管细胞中,哇巴因通过细胞内游离钙介导增强福斯高林对腺苷酸环化酶的激活,且细胞外钙是哇巴因动员细胞内钙的重要来源。