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首页> 外文期刊>Life sciences >Peroxynitrite induces arteriolar smooth muscle cells membrane hyperpolarization with arteriolar hyporeactivity in rats
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Peroxynitrite induces arteriolar smooth muscle cells membrane hyperpolarization with arteriolar hyporeactivity in rats

机译:过氧亚硝酸盐诱导大鼠小动脉平滑肌细胞膜超极化并引起小动脉反应性降低

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Peroxynitrite (ONOO-) has been recently known to act as a potent cytotoxin during pathogenesis of various diseases. This study aimed to investigate the possible effect of ONOO- on the cremaster muscle arteriolar reactivity in response to noradrenaline and subsequently determined whether membrane hyperpolarization and potassium channel activation were involved in ONOO--induced alteration of arteriolar reactivity. The results demonstrated that 1) ONOO- could decrease arteriolar reactivity in a time- and concentration-dependent manner with no significant alteration of arteriolar diameter; 2) Superfusion with 20 muM ONOO- over 40 minutes showed slight but not significant influence on the resting potential (Em) of arteriolar smooth muscle cells (ASMCs). However, ASMCs subjected to 50 or 100 muM ONOO- administration were significantly hyperpolarized. As control, treatment with 50 muM decomposed ONOO- or Kreb's solution had little effect on the Em of ASMCs; 3) ONOO--induced arteriolar hyporeactivity could be greatly reversed by co-administration of KCl and partially by TEA. The above results indicated that membrane hyperpolarization and potassium channel activation were preferentially responsible for the reduction of cremaster muscle arteriolar reactivity after exposure to ONOO-. (C) 2003 Elsevier Inc. All rights reserved. [References: 38]
机译:近来,过氧亚硝酸盐(ONOO-)在各种疾病的发病机理中起有效的细胞毒素作用。这项研究旨在调查ONOO-对去甲肾上腺素的反应对提睾肌小动脉反应性的可能影响,并随后确定ONOO引起的小动脉反应性改变是否涉及膜超极化和钾通道激活。结果表明:1)ONOO-可以以时间和浓度依赖性方式降低小动脉反应性,而没有明显改变小动脉直径; 2)在40分钟内用20μMONOO-灌注对小动脉平滑肌细胞(ASMC)的静息电位(Em)产生轻微但不显着的影响。但是,接受50或100μMONOO-给药的ASMC明显超极化。作为对照,用50μM分解的ONOO-或Kreb溶液处理对ASMC的Em几乎没有影响。 3)通过同时施用KCl和部分TEA可以大大扭转ONOO诱导的小动脉反应性降低。以上结果表明,膜超极化和钾离子通道激活是引起ONOO-后提睾肌小动脉反应性降低的主要原因。 (C)2003 Elsevier Inc.保留所有权利。 [参考:38]

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