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钾离子通道作为治疗胃肠运动障碍的潜在靶点。

K+ channels as potential targets for the treatment of gastrointestinal motor disorders.

作者信息

Currò Diego

机构信息

Institute of Pharmacology, School of Medicine, Catholic University of the Sacred Heart, L.go F. Vito 1, 00168 Rome, Italy.

出版信息

Eur J Pharmacol. 2014 Jun 15;733:97-101. doi: 10.1016/j.ejphar.2014.03.049. Epub 2014 Apr 13.

Abstract

K(+) channels play important functional roles in excitable cells, as neurons and muscle cells. The activation or inhibition of K(+) channels hyperpolarizes or depolarizes the cell membrane, respectively. These effects determine in the smooth muscle decrease or increase in Ca(2+) influx through voltage-gated Ca(2+) (CaV1.2) channels and relaxation or contraction, respectively. Recent studies highlight the importance of voltage-dependent type 7 K(+) (KV7 or KCNQ) channels in regulating muscle tone and contractility in stomach and colon. KV7 channels, that include 5 subtypes (KV7.1-7.5), are activated at relatively negative potential values, close to those of the resting membrane potential for the smooth muscle cells of some segments of the gastrointestinal tract. Thus, they contribute to set the resting membrane potential and their blockade induces increase in smooth muscle contractility in stomach and colon. In addition, KV7 channel activation produces profound relaxations of gastric and colonic smooth muscle. Therefore, KV7 channel activators could be used to relax the smooth muscle and relieve symptoms in diseases such as functional dyspepsia and irritable bowel syndrome with prevalent diarrhea. The discovery of activators selective for the channel subtypes present in the smooth muscle, mainly KV7.4 and 7.5, would allow avoiding adverse cardiac and nervous system effects. A further step forward would be characterizing putative differences among the KV7 channel subtypes expressed in the various smooth muscles and synthesizing molecules specific for the gastrointestinal smooth muscle.

摘要

钾离子通道在可兴奋细胞(如神经元和肌肉细胞)中发挥着重要的功能作用。钾离子通道的激活或抑制分别使细胞膜超极化或去极化。这些效应分别决定了平滑肌中通过电压门控钙通道(CaV1.2)的钙离子内流减少或增加,以及平滑肌舒张或收缩。最近的研究强调了电压依赖性7型钾离子通道(KV7或KCNQ)在调节胃和结肠肌张力及收缩性方面的重要性。KV7通道包括5个亚型(KV7.1 - 7.5),在相对负的电位值下被激活,接近胃肠道某些节段平滑肌细胞的静息膜电位。因此,它们有助于设定静息膜电位,其阻断会导致胃和结肠平滑肌收缩性增加。此外,KV7通道激活可使胃和结肠平滑肌产生显著舒张。因此,KV7通道激活剂可用于舒张平滑肌,并缓解功能性消化不良和腹泻型肠易激综合征等疾病的症状。发现对平滑肌中存在的通道亚型(主要是KV7.4和7.5)具有选择性的激活剂,将有助于避免心脏和神经系统的不良影响。进一步的进展将是明确在各种平滑肌中表达的KV7通道亚型之间的假定差异,并合成针对胃肠道平滑肌的特异性分子。

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