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KIR channels function as electrical amplifiers in rat vascular smooth muscle

机译:KIR通道在大鼠血管平滑肌中用作电放大器

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摘要

Strong inward rectifying K+ (KIR) channels have been observed in vascular smooth muscle and can display negative slope conductance. In principle, this biophysical characteristic could enable KIR channels to 'amplify' responses initiated by other K+ conductances. To test this, we have characterized the diversity of smooth muscle KIR properties in resistance arteries, confirmed the presence of negative slope conductance and then determined whether KIR inhibition alters the responsiveness of middle cerebral, coronary septal and third-order mesenteric arteries to K+ channel activators. Our initial characterization revealed that smooth muscle KIR channels were highly expressed in cerebral and coronary, but not mesenteric arteries. These channels comprised KIR 2.1 and 2.2 subunits and electrophysiological recordings demonstrated that they display negative slope conductance. Computational modelling predicted that a KIR-like current could amplify the hyperpolarization and dilatation initiated by a vascular K+ conductance. This prediction was consistent with experimental observations which showed that 30 μ m Ba2+ attenuated the ability of K+ channel activators to dilate cerebral and coronary arteries. This attenuation was absent in mesenteric arteries where smooth muscle KIR channels were poorly expressed. In summary, smooth muscle KIR expression varies among resistance arteries and when channel are expressed, their negative slope conductance amplifies responses initiated by smooth muscle and endothelial K+ conductances. These findings highlight the fact that the subtle biophysical properties of KIR have a substantive, albeit indirect, role in enabling agonists to alter the electrical state of a multilayered artery. © 2008 The Authors. Journal compilation © 2008 The Physiological Society.
机译:在血管平滑肌中已观察到强大的向内整流K +(KIR)通道,可显示负的斜率电导。原则上,这种生物物理特性可以使KIR通道“放大”由其他K +电导引发的响应。为了测试这一点,我们表征了阻力动脉中平滑肌KIR特性的多样性,确认了负斜率电导的存在,然后确定KIR抑制作用是否改变了大脑中部,冠状动脉间隔和三级肠系膜动脉对K +通道激活剂的反应性。我们的初步特征显示,平滑肌KIR通道在脑和冠状动脉中高表达,而在肠系膜动脉中则不高。这些通道包含KIR 2.1和2.2亚基,电生理记录表明它们显示出负的斜率电导。计算模型预测,类似KIR的电流可以放大由血管K +电导引起的超极化和扩张。该预测与实验观察一致,实验观察表明30μm Ba2 +减弱了K +通道激活剂扩张脑和冠状动脉的能力。在平滑肌KIR通道表达较差的肠系膜动脉中没有这种衰减。总之,平滑肌KIR表达在阻力动脉之间变化,当表达通道时,其负斜率电导会放大由平滑肌和内皮K +电导引发的反应。这些发现突出了这样一个事实,即KIR的微妙的生物物理特性在使激动剂改变多层动脉的电状态方面具有实质性的作用,尽管是间接的。 ©2008作者。期刊编辑©2008生理学会。

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