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A redox-based mechanism for the neuroprotective and neurodestructive effects of nitric oxide and related nitroso-compounds.一种基于氧化还原的机制,用于解释一氧化氮及相关亚硝基化合物的神经保护和神经破坏作用。
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A monovalent ion-selective cation current activated by noradrenaline in smooth muscle cells of rabbit ear artery.去甲肾上腺素激活的兔耳动脉平滑肌细胞中的单价离子选择性阳离子电流。
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一氧化氮对大鼠棕色脂肪组织中钙激活非选择性阳离子通道活性的调节作用

Modulation of calcium-activated non-selective cation channel activity by nitric oxide in rat brown adipose tissue.

作者信息

Koivisto A, Nedergaard J

机构信息

Wenner-Gren Institute, Arrhenius Laboratories F3, Stockholm University, Sweden.

出版信息

J Physiol. 1995 Jul 1;486 ( Pt 1)(Pt 1):59-65. doi: 10.1113/jphysiol.1995.sp020790.

DOI:10.1113/jphysiol.1995.sp020790
PMID:7562644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1156496/
Abstract
  1. Single-channel calcium-activated non-selective cation currents from isolated rat brown fat cells were measured using the inside-out patch configuration of the patch-clamp technique. The existence of a possible modulatory effect of nitric oxide on the putative redox-modulatory site located on the intracellular side of the non-selective cation channel was investigated. 2. The nitric oxide-releasing substances nitroglycerin, sodium nitroprusside, S-nitrosocysteine and S-nitroso-N-acetyl-D,L-penicillamine (all at 100 microM) were able to block channel activity almost completely. 3. In each case the blockade was persistent and could not be washed away. Dithiothreitol (DTT, 2 mM) was able to reverse the blockade to a large extent, whereas oxidized DTT (2 mM) was without effect. 4. It was concluded that nitric oxide can modulate non-selective cation channel activity by oxidizing sulfhydryl groups and that this effect can be reversed by reduction.
摘要
  1. 使用膜片钳技术的内面向外膜片构型,测量了分离的大鼠棕色脂肪细胞的单通道钙激活非选择性阳离子电流。研究了一氧化氮对位于非选择性阳离子通道胞内侧的假定氧化还原调节位点可能存在的调节作用。2. 释放一氧化氮的物质硝酸甘油、硝普钠、S-亚硝基半胱氨酸和S-亚硝基-N-乙酰-D,L-青霉胺(均为100微摩尔)几乎能完全阻断通道活性。3. 在每种情况下,阻断都是持久的,无法被洗脱。二硫苏糖醇(DTT,2毫摩尔)能在很大程度上逆转这种阻断,而氧化型DTT(2毫摩尔)则没有效果。4. 得出的结论是,一氧化氮可通过氧化巯基来调节非选择性阳离子通道活性,且这种作用可通过还原作用逆转。