醛固酮对大鼠肾脏蛋白激酶C α和α 1钠钾腺苷三磷酸酶蛋白表达的快速作用

S. Eiam-Ong, Kittisak Sinphitukkul, K. Manotham, S. Eiam‐Ong
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引用次数: 8

摘要

先前的体外研究表明,醛固酮能快速刺激蛋白激酶C α (PKC α),激活Na, k - atp酶的α (α) 1亚型,从而增强其活性。然而,没有体内数据表明醛固酮同时对PKC α和α1- na, k - atp酶的肾脏蛋白表达有快速影响。本研究进一步研究了这些蛋白的表达。雄性Wistar大鼠腹腔注射生理盐水或醛固酮(150 μg/kg BW)。30分钟后,分别用Western blot和免疫组化检测PKC α和α1- na、k - atp酶蛋白的丰度和定位。给药后,血浆醛固酮水平从1,251.95±13.83上升至6,521.78±209.92 pmol/L。Western blot结果显示,醛固酮可使肾脏PKC α(匀浆样品)和α1- na、k - atp酶(质膜)的蛋白丰度分别提高约50%和30% (P<0.05)。免疫组化检查显示,假手术组髓质中PKC α蛋白表达明显。醛固酮刺激了皮层和髓质的表达,并使近端曲小管(PCT)从基底外侧向管腔侧移位。在α1-Na、k - atp酶蛋白表达方面,假手术大鼠远曲小管、集管和粗大的升肢均有较强的免疫染色。醛固酮升高PCT和髓质集管(MCD)的表达。这项体内研究首次同时证明醛固酮可迅速提高大鼠肾脏中PKC α和α1- na、k - atp酶蛋白的丰度。皮层和髓质的免疫反应均受到刺激。PKC α表达的影响较大,而α1- na、k - atp酶的改变仅在PT和MCD中观察到。醛固酮本身刺激Na, k - atp酶蛋白表达可能通过PKC活化发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid Action of Aldosterone on Protein Expressions of Protein Kinase C Alpha and Alpha1 Sodium Potassium Adenosine Triphosphatase in Rat Kidney
Previous in vitro studies showed that aldosterone rapidly stimulates protein kinase C alpha (PKC α) that could activate alpha (α) 1 isoform of Na, K-ATPase and then enhances its activity. There are, however, no in vivo data that demonstrate the rapid effects of aldosterone on renal protein expressions of PKC α and α1-Na, K-ATPase simultaneously. The present study further investigates the expression of these proteins. Male Wistar rats were intraperitoneally injected with normal saline solution or aldosterone (150 μg/kg BW). After 30 minutes, abundances and localizations of PKC α and α1-Na, K-ATPase proteins were determined by Western blot analysis and immunohistochemistry, respectively. Aldosterone  administration significantly increased plasma aldosterone levels from 1,251.95 ± 13.83 to 6,521.78 ± 209.92 pmol/L. By Western blot analysis, aldosterone enhanced renal protein abundances of PKC α (homogenate samples) and α1-Na, K-ATPase (plasma membrane) approximately 50% and 30%, respectively (P<0.05). From immunohistochemistry examination in sham group, the protein expression of PKC α was prominent in the medulla. Aldosterone stimulated the expression both in the cortex and medulla with the translocation from the basolateral to luminal side of the proximal convoluted tubule (PCT). As for α1-Na, K-ATPase protein expression, the sham rats showed a strong immunostaining in the distal convoluted tubules, collecting ducts, and thick ascending limbs. Aldosterone elevated the expression in the PCT and medullary collecting duct (MCD). This in vivo study is the first to demonstrate simultaneously that aldosterone rapidly elevates PKC α and α1-Na, K-ATPase protein abundances in rat kidney. Both immunoreactivities were stimulated in the cortex and medulla. The greater affected areas were noted for PKC α expression, whereas the alterations of α1-Na, K-ATPase were observed only in the PT and MCD. The stimulation of Na, K-ATPase protein expression by aldosterone, per se, may occur through PKC activation.
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