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槲皮素和NPPB诱导醛固酮对肾上皮细胞钠吸收及上皮钠通道(ENaC)表达作用的减弱。

Quercetin and NPPB-induced diminution of aldosterone action on Na+ absorption and ENaC expression in renal epithelium.

作者信息

Fujimoto Shin-Ichiro, Niisato Naomi, Sugimoto Tohru, Marunaka Yoshinori

机构信息

Department of Molecular Cell Physiology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.

出版信息

Biochem Biophys Res Commun. 2005 Oct 21;336(2):401-7. doi: 10.1016/j.bbrc.2005.08.096.

Abstract

In renal epithelial A6 cells, aldosterone applied for 24 h increased the transepithelial Cl- secretion over 30-fold due to activation of the Na+/K+/2Cl- cotransporter and stimulated the transepithelial Na+ absorption, activity of epithelial Na+ channel (ENaC), and alpha-ENaC mRNA expression. The stimulatory action of aldosterone on the transepithelial Na+ absorption, ENaC activity, and alpha-ENaC mRNA expression was diminished by 24h-pretreatment with quercetin (an activator of Na+/K+/2Cl- cotransporter participating in Cl- entry into the cytosolic space) or 5-nitro 2-(3-phenylpropylamino)benzoate (NPPB) (a blocker of Cl- channel participating in Cl- release from the cytosolic space), while 24h-pretreatment with bumetanide (a blocker of Na+/K+/2Cl- cotransporter) enhanced the stimulatory action of aldosterone on transepithelial Na+ absorption. On the other hand, under the basal (aldosterone-unstimulated) condition, quercetin, NPPB or bumetanide had no effect on transepithelial Na+ absorption, activity of ENaC or alpha-ENaC mRNA expression. These observations suggest that although aldosterone shows overall its stimulatory action on ENaC (transepithelial Na+ transport), aldosterone has an inhibitory action on ENaC (transepithelial Na+ transport) via activation of the Na+/K+/2Cl- cotransporter, and that modification of activity of Cl- transporter/channel participating in the transepithelial Cl- secretion influences the aldosterone-stimulated ENaC (transepithelial Na+ transport).

摘要

在肾上皮A6细胞中,应用醛固酮24小时可使跨上皮氯离子分泌增加30多倍,这是由于钠/钾/2氯离子协同转运体的激活,并且可刺激跨上皮钠吸收、上皮钠通道(ENaC)活性以及α-ENaC信使核糖核酸表达。醛固酮对跨上皮钠吸收、ENaC活性以及α-ENaC信使核糖核酸表达的刺激作用,在用槲皮素(参与氯离子进入胞质空间的钠/钾/2氯离子协同转运体的激活剂)或5-硝基2-(3-苯丙基氨基)苯甲酸(NPPB,参与氯离子从胞质空间释放的氯离子通道阻滞剂)预处理24小时后减弱,而用布美他尼(钠/钾/2氯离子协同转运体阻滞剂)预处理24小时则增强了醛固酮对跨上皮钠吸收的刺激作用。另一方面,在基础(未用醛固酮刺激)条件下,槲皮素、NPPB或布美他尼对跨上皮钠吸收、ENaC活性或α-ENaC信使核糖核酸表达没有影响。这些观察结果表明,尽管醛固酮总体上对ENaC(跨上皮钠转运)表现出刺激作用,但醛固酮通过激活钠/钾/2氯离子协同转运体对ENaC(跨上皮钠转运)具有抑制作用,并且参与跨上皮氯离子分泌的氯离子转运体/通道活性的改变会影响醛固酮刺激的ENaC(跨上皮钠转运)。

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