...
首页> 外文期刊>American Journal of Physiology >Time-dependent stimulation by aldosterone of blocker-sensitive ENaCs in A6 epithelia.
【24h】

Time-dependent stimulation by aldosterone of blocker-sensitive ENaCs in A6 epithelia.

机译:醛固酮在A6上皮细胞中对阻滞剂敏感的ENaC的时间依赖性刺激。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

To study and define the early time-dependent response (< or = 6 h) of blocker-sensitive epithelial Na+ channels (ENaCs) to stimulation of Na+ transport by aldosterone, we used a new modified method of blocker-induced noise analysis to determine the changes of single-channel current (iNa) channel open probability (Po), and channel density (NT) under transient conditions of transport as measured by macroscopic short-circuit currents (Isc). In three groups of experiments in which spontaneous baseline rates of transport averaged 1.06, 5.40, and 15.14 microA/cm2, stimulation of transport occurred due to increase of blocker-sensitive channels. NT varied linearly over a 70-fold range of transport (0.5-35 microA/cm2). Relatively small and slow time-dependent but aldosterone-independent decreases of Po occurred during control (10-20% over 2 h) and aldosterone experimental periods (10-30% over 6 h). When the Po of control and aldosterone-treated tissues was examined over the 70-fold extended range of Na+ transport, Po was observed to vary inversely with Isc, falling from approximately 0.5 to approximately 0.15 at the highest rates of Na+ transport or approximately 25% per 3-fold increase of transport. Because decreases of Po from any source cannot explain stimulation of transport by aldosterone, it is concluded that the early time-dependent stimulation of Na+ transport in A6 epithelia is due exclusively to increase of apical membrane NT.
机译:为了研究和定义阻滞剂敏感的上皮Na +通道(ENaCs)对醛固酮刺激Na +转运的早期时间依赖性反应(<或= 6 h),我们使用了一种新的改良的阻滞剂诱导的噪声分析方法来确定通过宏观短路电流(Isc)测量的瞬态传输条件下单通道电流(iNa)的通道开路概率(Po)和通道密度(NT)的变化。在三组实验中,运输的自发基线速率平均为1.06、5.40和15.14 microA / cm2,由于对阻断剂敏感的通道增加,刺激了运输。 NT在运输的70倍范围内(0.5-35 microA / cm2)线性变化。在控制期间(2小时内10-20%)和醛固酮实验期间(6小时内10-30%)发生的Po相对较小且缓慢的时间依赖性,但与醛固酮无关。当在Na +转运的70倍扩展范围内检查对照和醛固酮治疗组织的Po时,观察到Po与Isc成反比,最高Na +转运率从约0.5降至约0.15或约25%每增加3倍的运输量。由于任何来源的Po减少都不能解释醛固酮对运输的刺激,因此可以得出结论,A6上皮细胞Na +运输的早期时间依赖性刺激完全是由于顶膜NT的增加所致。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号