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慢性代谢性酸中毒会增加大鼠肾脏中NHE3蛋白的丰度。

Chronic metabolic acidosis increases NHE3 protein abundance in rat kidney.

作者信息

Ambühl P M, Amemiya M, Danczkay M, Lötscher M, Kaissling B, Moe O W, Preisig P A, Alpern R J

机构信息

Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75235-8856, USA.

出版信息

Am J Physiol. 1996 Oct;271(4 Pt 2):F917-25. doi: 10.1152/ajprenal.1996.271.4.F917.

Abstract

Chronic metabolic acidosis increases the activity of the proximal tubule apical membrane Na/H antiporter, which is encoded predominantly by the NHE3 isoform. The present studies examined the effect of chronic metabolic acidosis on apical membrane NHE3 protein abundance in rats. Rats subjected to NH4Cl in their drinking water developed a metabolic acidosis, which decreased in magnitude over 14 days. During this time, renal cortical brush-border membrane NHE3 protein abundance, assessed by Western blot, increased progressively (28% at 3 days, 59% at 7 days, and 90% at 14 days). Immunohistochemistry revealed that the acidosis-induced increase in NHE3 abundance occurred in the apical membranes of the S1 and S2 segments of the proximal tubule and the thick ascending limb. NHE3 mRNA abundance was not significantly increased in these animals, whereas phosphoenolpyruvate carboxykinase and glyceraldehyde-3-phosphate dehydrogenase mRNA abundances were significantly increased. These studies demonstrate that the increase in Na/H antiporter activity seen in metabolic acidosis involves an increase in NHE3 protein abundance, which is distributed along the proximal tubule and the thick ascending limb. In addition, these studies suggest that a component of this adaptation is unrelated to changes in NHE3 mRNA abundance.

摘要

慢性代谢性酸中毒会增加近端小管顶端膜钠氢交换体的活性,该交换体主要由NHE3亚型编码。本研究检测了慢性代谢性酸中毒对大鼠顶端膜NHE3蛋白丰度的影响。给大鼠饮用含氯化铵的水会导致代谢性酸中毒,其严重程度在14天内逐渐减轻。在此期间,通过蛋白质印迹法评估,肾皮质刷状缘膜NHE3蛋白丰度逐渐增加(3天时增加28%,7天时增加59%,14天时增加90%)。免疫组织化学显示,酸中毒诱导的NHE3丰度增加发生在近端小管S1和S2段以及髓袢升支粗段的顶端膜。这些动物的NHE3 mRNA丰度没有显著增加,而磷酸烯醇式丙酮酸羧激酶和甘油醛-3-磷酸脱氢酶mRNA丰度显著增加。这些研究表明,在代谢性酸中毒中观察到的钠氢交换体活性增加涉及NHE3蛋白丰度的增加,其分布在近端小管和髓袢升支粗段。此外,这些研究表明这种适应性变化的一个组成部分与NHE3 mRNA丰度的变化无关。

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