Toda H, Noguchi T, Miyagishi A, Ito N, Umekawa K, Sato Y, Kitano M, Ohashi N
Research Center, Sumitomo Pharmaceutical Co. Ltd., Osaka, Japan.
Int J Tissue React. 1999;21(3):61-70.
We investigated the effects of SM-15681 (N-(aminoiminomethyl)-1-methyl-1H-indole-2-carboxamide monohydrochloride) on Na+/H+ exchange activity in the myocardium and in ischemic and hypoxic injury in isolated perfused rat hearts. These effects were compared with those of ethylisopropyl amiloride (EIPA). Na+/H+ exchange activity was studied with a NH4Cl prepulse technique under HCO3(-)-free conditions. SM-15681 (10(-8)-10(-7) M) inhibited pH recovery of acidosis in the rat myocardium in a concentration-dependent manner and the IC50 value of SM-15681 (80 nM) was similar to that of EIPA. In perfused rat hearts, SM-15681 (10(-6) M) and EIPA (10(-6) M) significantly improved cardiac functions and prevented enzyme release and abnormal elevation of tissue Ca2+ content during 20 min of reperfusion after 40 min of ischemia and 20 min of reoxygenation after 30 min of hypoxia. We conclude that an Na+/H+ exchange inhibitor, SM-15681, shows cardioprotective effects on ischemia/reperfusion and hypoxia/reoxygenation injury. Our results also support the hypothesis that Na+/H+ exchange contributes to the pathophysiology of cardiac ischemic reperfusion injury.
我们研究了SM-15681(N-(氨基亚氨基甲基)-1-甲基-1H-吲哚-2-甲酰胺盐酸盐)对大鼠心肌中Na+/H+交换活性以及对离体灌注大鼠心脏缺血和缺氧损伤的影响。将这些影响与乙基异丙基氨氯吡脒(EIPA)的影响进行了比较。在无HCO3(-)条件下,采用NH4Cl预脉冲技术研究Na+/H+交换活性。SM-15681(10(-8)-10(-7) M)以浓度依赖性方式抑制大鼠心肌酸中毒时的pH恢复,且SM-15681的IC50值(80 nM)与EIPA相似。在灌注大鼠心脏中,SM-15681(10(-6) M)和EIPA(10(-6) M)在缺血40分钟后再灌注20分钟以及缺氧30分钟后再给氧20分钟期间,显著改善心脏功能并防止酶释放和组织Ca2+含量异常升高。我们得出结论,Na+/H+交换抑制剂SM-15681对缺血/再灌注和缺氧/再给氧损伤具有心脏保护作用。我们的结果还支持Na+/H+交换参与心脏缺血再灌注损伤病理生理学的假说。