首页 | 本学科首页   官方微博 | 高级检索  
检索        


Pharmacology of KB‐R7943: A Na+–Ca2+ exchange inhibitor
Authors:Md Shah Amran  Nobuo Homma  Keitaro Hashimoto
Abstract:The Na+–Ca2+ exchange (NCX) system plays a pivotal role in regulating intracellular Ca2+ concentration in cardiomyocytes, neuronal cells, kidney and a variety of other cells. It performs a particularly important function in regulating cardiac contractility and electrical activity. One of the leading NCX inhibitors is KB‐R9743 (KBR) that appears to exhibit selectivity for Ca2+‐influx‐mode NCX activity (reverse mode of NCX). In this article we reviewed pharmacology of KBR and provide a brief summary of studies with other NCX inhibitors, such as SEA0400 (SEA) and SN‐6 (SN). Potential clinical usefulness of KBR and other NCX inhibitors is still controversial but the reviewed findings may be helpful in designing more selective and clinically useful NCX inhibitors for the treatment of cardiac, neuronal and kidney diseases.
Keywords:Aconitine  Action potential duration (APD)  Acute renal failure (ARF)  Arrhythmias  Cardiomyocytes  Heart  Ischemia/reperfusion arrhythmia  KB‐R7943  Na+‐Ca2+ exchange (NCX1‐3)  NCX inhibitors  Ni2+  SEA0400  SN‐6
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号