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血管平滑肌钠氢交换体动力学及其被血管紧张素II激活的过程

Vascular smooth muscle Na+-H+ exchanger kinetics and its activation by angiotensin II.

作者信息

Vallega G A, Canessa M L, Berk B C, Brock T A, Alexander R W

机构信息

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts 02115.

出版信息

Am J Physiol. 1988 Jun;254(6 Pt 1):C751-8. doi: 10.1152/ajpcell.1988.254.6.C751.

Abstract

We have studied the kinetic properties of basal and angiotensin II (ANG II)-stimulated Na+-H+ exchange in cultured rat aortic smooth muscle cells. Initial rates of 22Na+ influx were measured in the presence of ouabain (1 mM) and bumetanide (0.1 mM) with and without amiloride after intracellular acidification by preincubation in Na-free media. The kinetics of amiloride (100 microM)-sensitive Na+ influx were studied under the following conditions: 1) constant intracellular pH (pHi; 6.8) and varying external Na+ (Na+o), which gave a Km of 23.6 +/- 2.0 (SD, n = 3) mM and a maximum velocity (Vmax) of 25 nmol.mg protein-1.min-1 (varying the amiloride concentration gave a Ki of 22 microM for inhibition under these conditions); and 2) constant Na+o (100 mM) and varying pHi (from 7.4 to 6.2), which indicated that amiloride-sensitive Na+ influx was stimulated by cell acidification when an outward H+ gradient was imposed. ANG II-stimulated amiloride-sensitive Na+ influx for up to 30 min with a half-maximal activation 10(-8) M. The pHi dependence from cell pH (pHi 7.2-6.2) of amiloride-sensitive Na+ influx stimulated by ANG II was similar to that of the basal values, a finding indicating that ANG II did not change the affinity of Na+-H+ exchange for intracellular H+. However, at pHi 6.8, ANG II increased the Vmax of amiloride-sensitive Na+ influx from 25 to 33 nmol.mg protein-1.min-1 and markedly decreased the Km for Na+o from 23.6 +/- 7.4 to 3.7 (SD, n = 4; P less than 0.005) mM.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们研究了培养的大鼠主动脉平滑肌细胞中基础状态及血管紧张素II(ANG II)刺激下的Na⁺-H⁺交换的动力学特性。在无钠培养基中预孵育使细胞内酸化后,于存在哇巴因(1 mM)和布美他尼(0.1 mM)的情况下,分别在有和没有氨氯吡咪的条件下测量²²Na⁺内流的初始速率。在以下条件下研究了氨氯吡咪(100 μM)敏感的Na⁺内流动力学:1)细胞内pH(pHi;6.8)恒定,细胞外Na⁺(Na⁺o)变化,得出米氏常数(Km)为23.6±2.0(标准差,n = 3)mM,最大速度(Vmax)为25 nmol·mg蛋白⁻¹·min⁻¹(在这些条件下改变氨氯吡咪浓度得出抑制作用的半数抑制浓度(Ki)为22 μM);2)Na⁺o恒定(100 mM),pHi变化(从7.4至6.2),这表明当施加外向H⁺梯度时,细胞酸化刺激氨氯吡咪敏感的Na⁺内流。ANG II刺激氨氯吡咪敏感的Na⁺内流长达30分钟,半数最大激活浓度为10⁻⁸M。ANG II刺激的氨氯吡咪敏感的Na⁺内流对细胞pH(pHi 7.2 - 6.2)的依赖性与基础值相似,这一发现表明ANG II并未改变Na⁺-H⁺交换对细胞内H⁺的亲和力。然而,在pHi 6.8时,ANG II使氨氯吡咪敏感的Na⁺内流的Vmax从25增加至33 nmol·mg蛋白⁻¹·min⁻¹,并使Na⁺o的Km从23.6±7.4显著降低至3.7(标准差,n = 4;P < 0.005)mM。(摘要截断于250字)

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