Iwamoto Takahiro, Kita Satomi
Department of Pharmacology, School of Medicine, Fukuoka University, Fukuoka, Japan.
Mol Cell Biochem. 2004 Apr;259(1-2):157-61. doi: 10.1023/b:mcbi.0000021367.42752.54.
The Na+/Ca2+ exchanger (NCX) is an ion transporter that exchanges Na+ and Ca2+ in either Ca2+ efflux or Ca2+ influx mode, depending on the ion gradients across the plasma membrane and the membrane potential. In heart, smooth muscle cells, neurons, and nephron cells, the NCX is thought to play an important role in the regulation of intracellular Ca2+ concentration. Recently, a novel selective inhibitor (KB-R7943 and SEA0400) of the Ca2+ influx mode of the NCX has been developed. NCX inhibitor is expected to be a pharmaceutical agent that offers effective protection against ischemia/reperfusion injury in several organs such as heart and kidney. Here, we summarize pharmacological profiles of KB-R7943 and SEA0400, the molecular mechanism of its action, and its future prospect as a novel pharmaceutical agent.
钠钙交换体(NCX)是一种离子转运体,它根据质膜两侧的离子梯度和膜电位,以钙外流或钙内流模式交换钠离子和钙离子。在心脏、平滑肌细胞、神经元和肾单位细胞中,NCX被认为在调节细胞内钙离子浓度方面发挥着重要作用。最近,已经开发出一种新型的NCX钙内流模式选择性抑制剂(KB-R7943和SEA0400)。NCX抑制剂有望成为一种药物,为心脏和肾脏等多个器官的缺血/再灌注损伤提供有效的保护。在此,我们总结了KB-R7943和SEA0400的药理学特性、其作用的分子机制以及作为新型药物的未来前景。