Laboratory of Intracellular Ion Channels, Nencki Institute of Experimental Biology, Warsaw, Poland.
Toxicol Mech Methods. 2004;14(1-2):59-61. doi: 10.1080/15376520490257482.
It has recently been reported that large-conductance calcium-cation-activated potassium channels, also known as BK(Ca)-type potassium channels, are present in the inner membranes of cardiac cell mitochondria. It was also shown that the BK(Ca)-channel opener NS1619 (1,3-dihydro-1-[2-hydroxy-5-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-2H-benzimidazol-2-one) protects the heart against ischemic damage. In the present study we investigated the effects of NS1619 on the function of isolated cardiac mitochondria. In particular, we examined the influence of NS1619 on mitochondrial membrane potential and mitochondrial respiration. We showed that NS1619 decreases the mitochondrial membrane potential and inhibits the mitochondrial respiratory chain. Our results demonstrate that the protection induced by this channel opener in the heart may also be caused by pharmacological preconditioning through the inhibition of the mitochondrial respiratory chain.
最近有报道称,大电导钙激活阳离子型钾通道,也称为 BK(Ca)-型钾通道,存在于心肌细胞线粒体的内膜中。研究还表明,BK(Ca)-通道 opener NS1619(1,3-二氢-1-[2-羟基-5-(三氟甲基)苯基]-5-(三氟甲基)-2H-苯并咪唑-2-酮)可保护心脏免受缺血损伤。在本研究中,我们研究了 NS1619 对分离的心肌线粒体功能的影响。特别是,我们研究了 NS1619 对线粒体膜电位和线粒体呼吸的影响。结果表明,NS1619 降低线粒体膜电位并抑制线粒体呼吸链。我们的结果表明,这种通道 opener 在心脏中诱导的保护作用也可能是通过抑制线粒体呼吸链引起的药理学预处理所致。