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牛蛙皮肤(豹蛙)主细胞中的pH值:氨氯吡咪的作用及电位

pH in principal cells of frog skin (Rana pipiens): effects of amiloride and potential.

作者信息

Drewnowska K, Biber T U

机构信息

Department of Physiology, Medical College of Virginia, Richmond 23298.

出版信息

Am J Physiol. 1988 Nov;255(5 Pt 2):F922-9. doi: 10.1152/ajprenal.1988.255.5.F922.

Abstract

Intracellular pH (pHi) and apical cell membrane potential (Va) were determined in principal cells of frog skin (Rana pipiens) with double-barrel micro-electrodes. In the Northern and Southern varieties, respectively, pHi is 0.38 and 0.26 pH units below bath pH. Amiloride, applied apically, causes reversible intracellular acidification at concentrations of 10(-5) M or higher. Voltage clamp-induced hyperpolarization and depolarization of Va result in intracellular acidification and alkalinization, respectively. This response of pHi is inhibited or abolished when the apical side is treated with 10(-3) M 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid (DIDS). Amiloride-induced intracellular acidification is not exclusively due to the hyperpolarization of Va that accompanies amiloride treatment since 1) amiloride causes greater acidification than equivalent voltage clamp-induced hyperpolarization of Va, 2) amiloride-induced acidification persists in DIDS-treated tissues, and 3) there is no correlation between hyperpolarization of Va and intracellular acidification occurring after amiloride. We conclude that pHi is below the extracellular pH. Amiloride causes intracellular acidification that may be in part connected with hyperpolarization of Va. However, a major component of amiloride-induced acidification is due to other factors, possibly inhibition of apical Na+-H+ exchange. The inhibitory effect of apically applied DIDS suggests that the voltage dependent changes in pHi are related to movement of HCO3 (or OH) ions across the apical cell membrane.

摘要

使用双管微电极测定了牛蛙皮肤(豹蛙)主细胞中的细胞内pH值(pHi)和顶端细胞膜电位(Va)。在北方和南方品种中,pHi分别比浴液pH值低0.38和0.26个pH单位。从顶端施加的氨氯吡咪在浓度为10^(-5) M或更高时会导致可逆的细胞内酸化。电压钳诱导的Va超极化和去极化分别导致细胞内酸化和碱化。当顶端侧用10^(-3) M 4,4'-二异硫氰基芪-2,2'-二磺酸(DIDS)处理时,pHi的这种反应受到抑制或消除。氨氯吡咪诱导的细胞内酸化并非完全归因于氨氯吡咪处理时伴随的Va超极化,因为:1)氨氯吡咪引起的酸化比等效电压钳诱导的Va超极化更大;2)氨氯吡咪诱导的酸化在DIDS处理的组织中持续存在;3)Va的超极化与氨氯吡咪处理后发生的细胞内酸化之间没有相关性。我们得出结论,pHi低于细胞外pH值。氨氯吡咪会导致细胞内酸化,这可能部分与Va的超极化有关。然而,氨氯吡咪诱导的酸化的主要成分是由于其他因素,可能是顶端Na+-H+交换的抑制。顶端施加DIDS的抑制作用表明,pHi的电压依赖性变化与HCO3(或OH)离子跨顶端细胞膜的移动有关。

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