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首页> 外文期刊>Biochemical Pharmacology >Cross talk of cAMP and flavone in regulation of cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel and Na+/K+/2Cl- cotransporter in renal epithelial A6 cells.
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Cross talk of cAMP and flavone in regulation of cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel and Na+/K+/2Cl- cotransporter in renal epithelial A6 cells.

机译:cAMP和黄酮的交互作用在肾上皮A6细胞中调节囊性纤维化跨膜电导调节剂(CFTR)Cl-通道和Na + / K + / 2Cl-共转运蛋白。

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We have reported that in renal epithelial A6 cells flavones stimulate the transepithelial Cl- secretion by activating the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel and/or the Na+/K+/2Cl- cotransporter. On the other hand, it has been established that cAMP activates the CFTR Cl- channel and the Na+/K+/2Cl- cotransporter. However, no information is available on the interaction between cAMP and flavones on stimulation of the CFTR Cl- channel and the Na+/K+/2Cl- cotransporter. To clarify the interaction between cAMP and flavones, we studied the regulatory mechanism of the CFTR Cl- channel and the Na+/K+/2Cl- cotransporter by flavones (apigenin, luteolin, kaempherol, and quercetin) under the basal and cAMP-stimulated conditions in renal epithelial A6 cells. Under the basal (cAMP-unstimulated) condition, these flavones stimulated the Cl- secretion by activating the Na+/K+/2Cl- cotransporter without any significant effects on the CFTR Cl- channel activity. On the other hand, these flavones diminished the activity of the cAMP-stimulated Na+/K+/2Cl- cotransporter without any significant effects on the CFTR Cl- channel activity. Interestingly, the level of the flavone-induced Cl- secretion under the basal condition was identical to that under the cAMP-stimulated condition. Based on these results, it is suggested that although both cAMP and flavones activate the Na+/K+/2Cl- cotransporter, these flavones have more powerful effects than cAMP on the Na+/K+/2Cl- cotransporter.
机译:我们已经报道,在肾上皮A6细胞中,黄酮通过激活囊性纤维化跨膜电导调节剂(CFTR)Cl-通道和/或Na + / K + / 2Cl-共转运蛋白刺激跨上皮Cl-分泌。另一方面,已经确定cAMP激活CFTR Cl-通道和Na + / K + / 2Cl-共转运蛋白。但是,尚无有关cAMP与黄酮相互作用刺激CFTR Cl-通道和Na + / K + / 2Cl-共转运蛋白的信息。为了阐明cAMP与黄酮之间的相互作用,我们研究了在基础和cAMP刺激条件下,黄酮(芹菜素,木犀草素,kaempherol和槲皮素)对CFTR Cl-通道和Na + / K + / 2Cl-共转运蛋白的调节机制。肾上皮A6细胞。在基础(未受cAMP刺激)条件下,这些黄酮通过激活Na + / K + / 2Cl-共转运蛋白刺激了Cl-分泌,而对CFTR Cl-通道活性没有任何显着影响。另一方面,这些黄酮减少了cAMP刺激的Na + / K + / 2Cl-共转运蛋白的活性,而对CFTR Cl-通道活性没有任何显着影响。有趣的是,基础条件下黄酮诱导的Cl分泌水平与cAMP刺激条件下的水平相同。基于这些结果,表明尽管cAMP和黄酮均激活Na + / K + / 2Cl-共转运蛋白,但这些黄酮对c +的Na + / K + / 2Cl-共转运蛋白具有更强的作用。

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