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哇巴因对培养的大鼠肾乳头集合管细胞中福斯高林诱导的环磷酸腺苷(cAMP)生成的增强作用。

Augmentation of forskolin-induced cAMP production by ouabain in rat renal papillary collecting tubule cells in culture.

作者信息

Ishikawa S, Saito T

机构信息

Department of Medicine, Jichi Medical School, Tochigi, Japan.

出版信息

Biochem Biophys Res Commun. 1990 Jan 15;166(1):411-6. doi: 10.1016/0006-291x(90)91960-z.

Abstract

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.

摘要

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。

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