Ohara F, Sugimoto T, Yamamoto N, Ohkubo K, Maeda K, Ozaki T, Seki J, Goto T
Department of Cardiovascular Diseases, Medicinal Biology Research Laboratories, Fujisawa Pharmaceutical Co., Ltd, Osaka, Japan.
J Cardiovasc Pharmacol. 1999 Dec;34(6):848-56. doi: 10.1097/00005344-199912000-00012.
This study describes the pharmacologic profile of a new Na+/H(+)-exchange inhibitor, FR183998, in anesthetized rats. FR183998 had a potent inhibitory effect on Na+/H+ exchange of rat lymphocytes with median inhibitory (IC50) value of 0.3 nM. Treatment with FR183998 (0.01-0.32 mg/kg, i.v.) reduced or completely abolished ventricular fibrillation and mortality induced by 5-min ischemia followed by reperfusion, when it was administered not only 5 min before ischemia but also 1 min before reperfusion. Myocardial infarct size induced by 30-min ischemia and 60-min reperfusion was reduced significantly in a dose-dependent manner by FR183998 (0.1-1.0 mg/kg, i.v.) when the drug was administered preischemically or at an early phase of ischemia. The ventricular tachycardia and the ventricular fibrillation observed during the ischemic period also were suppressed significantly. These results indicate that FR183998 has a strong inhibitory effect on Na+/H+ exchange and suggest that treatment with FR183998 either before or immediately after the onset of ischemia can prevent the occurrence of arrhythmias and myocardial cell necrosis in situations of ischemia and reperfusion.
本研究描述了一种新型钠氢交换抑制剂FR183998在麻醉大鼠中的药理学特性。FR183998对大鼠淋巴细胞的钠氢交换具有强效抑制作用,中位抑制(IC50)值为0.3 nM。当在缺血前5分钟以及再灌注前1分钟静脉注射FR183998(0.01 - 0.32 mg/kg)时,可减轻或完全消除由5分钟缺血后再灌注诱导的室颤和死亡率。当在缺血前或缺血早期静脉注射FR183998(0.1 - 1.0 mg/kg)时,由30分钟缺血和60分钟再灌注诱导的心肌梗死面积以剂量依赖方式显著减小。缺血期观察到的室性心动过速和室颤也受到显著抑制。这些结果表明FR183998对钠氢交换具有强烈抑制作用,并提示在缺血发作前或发作后立即用FR183998治疗可预防缺血和再灌注情况下心律失常和心肌细胞坏死的发生。