Zhou X, Wingo C S
Department of Physiology, College of Medicine, University of Florida, Gainesville.
Am J Physiol. 1992 Jul;263(1 Pt 2):F43-8. doi: 10.1152/ajprenal.1992.263.1.F43.
Previous studies suggest that enhancement of rubidium tracer (86Rb) lumen-to-bath efflux following removal of luminal Na is mediated in part by a Ba-insensitive pathway. To determine the role of a primary active K pump in this response, we examined the action of known inhibitors of H-K-ATPase (Sch 28080) and Na-K-ATPase (ouabain) on the 86Rb lumen-to-bath efflux coefficient (KRb). Luminal Sch 28080 (10 microM) significantly reduced KRb by 39 +/- 8.0% (P less than 0.05), whereas luminal ouabain (0.1 mM) reduced KRb by 10 +/- 14% (P = not significant), suggesting that a luminal H-K-ATPase mediates Rb efflux. To examine whether H-K-ATPase mediates Rb in KRb following removal of luminal Na, additional experiments were conducted to examine the effect of Sch 28080 on KRb in the presence and the absence of luminal Na. In the presence of luminal Na, 10 microM Sch 28080 reduced KRb by 15 +/- 5.0%. However, in the absence of luminal Na, 10 microM Sch 28080 decreased KRb by 48 +/- 8.2%. The percentage inhibition of KRb by Sch 28080 was significantly greater in the absence of luminal Na than in its presence (P less than 0.01), suggesting that the enhancement of KRb following removal of luminal Na is mediated in part by an H-K-ATPase pathway. In either case transepithelial voltage was not significantly altered. In contrast to the lack of effect of luminal ouabain, addition of 0.1 mM ouabain to the bath increased KRb (69.8 +/- 11.1 vs. 95.9 +/- 18.7 nm/s, P less than 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)
先前的研究表明,去除管腔钠后铷示踪剂(86Rb)从管腔到浴液的流出增强,部分是由钡不敏感途径介导的。为了确定原发性活性钾泵在这种反应中的作用,我们研究了已知的氢钾ATP酶抑制剂(Sch 28080)和钠钾ATP酶抑制剂(哇巴因)对86Rb从管腔到浴液的流出系数(KRb)的作用。管腔内的Sch 28080(10微摩尔)使KRb显著降低39±8.0%(P<0.05),而管腔内的哇巴因(0.1毫摩尔)使KRb降低10±14%(P无显著性差异),这表明管腔内的氢钾ATP酶介导铷流出。为了研究去除管腔钠后氢钾ATP酶是否介导KRb中的铷流出,进行了额外的实验,以研究在有和没有管腔钠的情况下Sch 28080对KRb的影响。在有管腔钠的情况下,10微摩尔Sch 28080使KRb降低15±5.0%。然而,在没有管腔钠的情况下,10微摩尔Sch 28080使KRb降低48±8.2%。Sch 28080对KRb的抑制百分比在没有管腔钠时显著高于有管腔钠时(P<0.01),这表明去除管腔钠后KRb的增强部分是由氢钾ATP酶途径介导的。在任何一种情况下,跨上皮电压均无显著改变。与管腔内哇巴因无作用相反,向浴液中加入0.1毫摩尔哇巴因可增加KRb(69.8±11.1对95.9±18.7纳米/秒,P<0.05)。(摘要截断于250字)