首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Elevation of intracellular calcium by muscarinic receptor activation induces a block of voltage-activated rat ether-à-go-go channels in a stably transfected cell line.
【2h】

Elevation of intracellular calcium by muscarinic receptor activation induces a block of voltage-activated rat ether-à-go-go channels in a stably transfected cell line.

机译:毒蕈碱受体激活引起的细胞内钙的升高在稳定转染的细胞系中诱导了电压激活的大鼠醚-去-去通道的阻断。

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

We have studied the properties of r-eag voltage-activated potassium channels in a stably transfected human embryonic kidney cell line. It was found that r-eag channels are rapidly and reversibly inhibited by a rise in intracellular calcium from 30 to 300 nM. The inhibition does not appear to depend on the activity of calcium-dependent kinases and phosphatases. The effect of calcium on r-eag channel activity was studied in inside-out membrane patches. Calcium inhibited r-eag channel activity with a mean IC50 of 67 nM. Activation of muscarinic receptors, generating calcium oscillations in the transfected cells, induced a synchronous inhibition of r-eag mediated outward currents. This shows that calcium can mediate r-eag current inhibition following muscarinic receptor activation. The data indicate that r-eag channels are calcium-inhibitable voltage-activated potassium channels.
机译:我们已经研究了稳定转染的人胚胎肾细胞系中r-eag电压激活的钾离子通道的特性。已发现,细胞内钙从30 nM升高到300 nM,可快速且可逆地抑制r-eag通道。抑制作用似乎不依赖于钙依赖性激酶和磷酸酶的活性。在由内而外的膜片中研究了钙对r-eag通道活性的影响。钙抑制r-eag通道活性,平均IC50为67 nM。毒蕈碱受体的激活在转染的细胞中产生钙振荡,从而诱导了r-eag介导的外向电流的同步抑制。这表明钙可在毒蕈碱受体激活后介导r-eag电流抑制。数据表明,r-eag通道是可抑制钙的电压激活的钾通道。

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