首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Pyridine nucleotide redox state parallels production of aldosterone in potassium-stimulated adrenal glomerulosa cells.
【2h】

Pyridine nucleotide redox state parallels production of aldosterone in potassium-stimulated adrenal glomerulosa cells.

机译:吡啶核苷酸的氧化还原状态与钾刺激的肾上腺肾小球细胞中醛固酮的产生平行。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Extracellular potassium ions (K+) raise the intracellular concentration of free Ca2+ ([Ca2+]i) by gating voltage-dependent Ca2+ channels and stimulate aldosterone production in adrenal glomerulosa cells. The pathway leading from calcium influx to increased steroid synthesis has not been completely elucidated. In the present study we demonstrate that the reduction of pyridine nucleotides known to be required for steroid hydroxylation is enhanced by K+ (4.1-8.4 mM) in single rat glomerulosa cells. The action of K+ was strictly dependent on the presence of extracellular Ca2+. Amytal, a blocker of site I of the mitochondrial respiratory chain, abolished the K+ effect, indicating a mitochondrial origin for the recorded changes. Supraphysiological K+ concentration (18 mM) resulted in a further increase in [Ca2+]i, while steroidogenesis was decreased as measured in cell suspensions. However, a possible explanation for this dichotomy is provided by the finding that the level of reduced pyridine nucleotides also decreased at supraphysiological K+ concentration.
机译:细胞外钾离子(K +)通过门控电压依赖性Ca2 +通道来提高游离Ca2 +([Ca2 +] i)的细胞内浓度,并刺激肾上腺肾小球细胞中醛固酮的产生。尚未完全阐明从钙流入到类固醇合成增加的途径。在本研究中,我们证明在单个大鼠肾小球细胞中,K +(4.1-8.4 mM)增强了甾族化合物羟基化所需的吡啶核苷酸的还原。 K +的作用严格取决于细胞外Ca2 +的存在。线粒体呼吸链的位点I的阻滞剂Amytal取消了K +效应,表明记录的变化的线粒体起源。超生理学K +浓度(18 mM)导致[Ca2 +] i进一步增加,而在细胞悬浮液中测得的类固醇生成减少。然而,通过发现在超生理学的K +浓度下还原的吡啶核苷酸的水平也下降,提供了对此二分法的可能解释。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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