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梗阻性肾病中兔髓质集合管细胞的转运缺陷

Transport defects of rabbit inner medullary collecting duct cells in obstructive nephropathy.

作者信息

Hwang S J, Harris H W, Otuechere G, Yalla S, Sullivan M R, Kashgarian M, Benos D J, Kleyman T R, Zeidel M L

机构信息

Research Service, West Roxbury Department of Veterans Affairs Medical Center, Massachusetts 02132.

出版信息

Am J Physiol. 1993 May;264(5 Pt 2):F808-15. doi: 10.1152/ajprenal.1993.264.5.F808.

Abstract

Urinary obstruction markedly reduces collecting duct Na+ reabsorption. To define the cellular mechanisms of this derangement in Na+ reabsorption in inner medullary collecting duct (IMCD) of obstructed kidneys, suspensions of intact IMCD cells and inner medulla plasma membranes (IMPM) were prepared from 24 h obstructed and untreated control kidneys. Oxygen consumption (QO2) studies revealed marked reductions in both amiloride-sensitive and ouabain-sensitive QO2 but not ouabain-insensitive QO2 in intact IMCD cells from obstructed, compared with control animals, indicating a reduction in oxygen-dependent transport activities of both the Na+ channel and the Na(+)-K(+)-adenosinetriphosphatase (ATPase). Amiloride-sensitive conductive 22Na+ uptake in intact IMCD cells from obstructed kidneys was significantly decreased by 45% at 10 s, 30 s, and 1-5 min (10 s: 2.42 +/- 0.63 vs. 4.49 +/- 0.64 nmol Na+ flux/mg protein, n = 7, P < 0.05; 1 min: 4.65 +/- 0.7 vs. 8.27 +/- 0.98 nmol Na+ flux/mg protein, n = 7, P < 0.05), indicating decreased activity of amiloride-sensitive Na+ channels in these cells. However, immunoblots of IMPM with antibodies to Na+ channel proteins did not show significant differences in content of Na+ channel proteins between membranes from obstructed and control groups. Ouabain-sensitive Na(+)-K(+)-ATPase activity in IMPM of obstructed kidneys was also reduced (61.1 +/- 18.1 vs. 152.6 +/- 25.8 nmol ATP degradation.min-1.mg protein-1, n = 6, P < 0.02), and immunoblots with monoclonal antibodies against the alpha 1- and beta-subunits of rabbit Na(+)-K(+)-ATPase showed a 51 +/- 7% reduction of both subunits in IMPM from obstructed kidneys (n = 4).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

尿路梗阻显著降低集合管对钠离子的重吸收。为了明确梗阻性肾病内髓集合管(IMCD)中钠离子重吸收紊乱的细胞机制,我们从梗阻24小时的肾脏和未处理的对照肾脏中制备了完整的IMCD细胞悬液和内髓质细胞膜(IMPM)。耗氧量(QO2)研究显示,与对照动物相比,梗阻组完整IMCD细胞中,氨氯地平敏感和哇巴因敏感的QO2均显著降低,但哇巴因不敏感的QO2未降低,这表明钠离子通道和钠钾腺苷三磷酸酶(ATP酶)的氧依赖性转运活性均降低。梗阻肾脏完整IMCD细胞中,氨氯地平敏感的22Na+摄取在10秒、30秒和1 - 5分钟时显著降低45%(10秒:2.42±0.63对4.49±0.64 nmol Na+通量/毫克蛋白,n = 7,P < 0.05;1分钟:4.65±0.7对8.27±0.98 nmol Na+通量/毫克蛋白,n = 7,P < 0.05),表明这些细胞中氨氯地平敏感的钠离子通道活性降低。然而,用钠离子通道蛋白抗体对IMPM进行免疫印迹分析显示,梗阻组和对照组细胞膜中钠离子通道蛋白含量无显著差异。梗阻肾脏IMPM中哇巴因敏感的钠钾ATP酶活性也降低(61.1±18.1对152.6±25.8 nmol ATP降解·分钟-1·毫克蛋白-1,n = 6,P < 0.02),用抗兔钠钾ATP酶α1和β亚基的单克隆抗体进行免疫印迹分析显示,梗阻肾脏IMPM中两个亚基均减少51±7%(n = 4)。(摘要截选至250字)

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