Fuchs J, Mainka L, Reifart N, Zimmer G
Arzneimittelforschung. 1986 Feb;36(2):209-12.
Bepridil (Cordium) was found to activate rat heart mitochondrial membrane-bound ATPase at concentrations of 10 nmol/l-10 mumol/l. By contrast, oligomycin-sensitive ATPase from beef heart mitochondria was inhibited at concentrations of 1-10 mumol/l. In both systems sensitivity toward the inhibitor oligomycin was reduced. Under the influence of the drug, RCR (coupling degree of electron transport to ATP synthesis), ST3 (oxygen uptake in presence of substrate and ADP) and OPR (oxidative phosphorylation rate, amount of ATP synthesized in mitochondrial metabolic state ST3) values are reduced, indicating partial inhibition of oxidative phosphorylation. At 0.25 mumol/l concentration of bepridil, in the isolated normoxic working rat heart preparation aortic flow was reduced to zero. No changes in oxidative phosphorylation parameters were found in mitochondria isolated from these preparations. In the isolated, working rat heart preparation bepridil at a concentration of 0.05 mumol/l reduced aortic flow to about 75% of its original value. In this preparation, no cardioprotective effects (neither on aortic flow nor on mitochondrial function) could be demonstrated during postischemic reperfusion. It is suggested, that in vitro mitochondrial activities of bepridil are not related to in vivo action of the drug.
发现苄普地尔(Cordium)在浓度为10纳摩尔/升至10微摩尔/升时可激活大鼠心脏线粒体膜结合的ATP酶。相比之下,来自牛心线粒体的寡霉素敏感ATP酶在浓度为1至10微摩尔/升时受到抑制。在这两个系统中,对抑制剂寡霉素的敏感性均降低。在药物的影响下,呼吸控制率(电子传递与ATP合成的偶联程度)、状态3(存在底物和ADP时的氧摄取)和氧化磷酸化率(在线粒体代谢状态3中合成的ATP量)值降低,表明氧化磷酸化受到部分抑制。在苄普地尔浓度为0.25微摩尔/升时,在分离的常氧工作大鼠心脏标本中,主动脉血流量降至零。从这些标本中分离出的线粒体中未发现氧化磷酸化参数有变化。在分离的工作大鼠心脏标本中,浓度为0.05微摩尔/升的苄普地尔可使主动脉血流量降至其原始值的约75%。在该标本中,在缺血后再灌注期间未显示出心脏保护作用(对主动脉血流量和线粒体功能均无作用)。有人提出,苄普地尔的体外线粒体活性与该药物的体内作用无关。