Kubow S, Wells P G
Faculty of Pharmacy, University of Toronto, Canada.
Mol Pharmacol. 1989 Apr;35(4):504-11.
Certain toxic effects of phenytoin are thought to result from its cytochrome P-450-catalyzed bioactivation to a reactive arene oxide intermediate that binds covalently to proteins. Using an in vitro system, we examined an alternative hypothesis based upon the cooxidation of phenytoin to a reactive free radical intermediate by prostaglandin synthetase (PGS), horseradish peroxidase, or thyroid peroxidase. Microsomes from hepatic, thyroid, seminal vesicular, or pulmonary tissues, or PGS or horseradish peroxidase, were incubated with the appropriate enzymatic cofactors to study activities of cytochromes P-450 (NADPH), PGS (arachidonic acid), thyroid peroxidase (guiaicol, H2O2), and horseradish peroxidase (H2O2). The production of potentially teratogenic, reactive phenytoin intermediates during in vitro incubations was estimated by the amount of radiolabeled phenytoin bound covalently to microsomal protein or bovine serum albumin and by the detection of a free radical intermediate using ESR spectrometry. Arachidonic acid-dependent bioactivation of phenytoin was demonstrated for purified PGS and ram seminal vesicles (RSV), as well as for liver, lung, and kidney. Optimal arachidonate concentrations varied substantially for different tissues. Arachidonate-dependent binding of phenytoin with PGS and RSV was reduced to baseline levels by coincubation with the cyclooxygenase inhibitor indomethacin. Hydrogen peroxide-dependent covalent binding of phenytoin was observed with thyroid peroxidase and horseradish peroxidase, and binding was significantly reduced in these systems and in PGS and RSV by coincubation with the peroxidase inhibitor methimazole. Glutathione, the antioxidants caffeic acid and butylated hydroxyanisole, and the free radical trapping agent alpha-phenyl-N-t-butylnitrone (PBN) all significantly reduced arachidonate-dependent phenytoin binding. Oxygen uptake was increased in a dose-dependent manner by the arachidonate-dependent bioactivation of phenytoin by PGS. ESR spin-trapping techniques using PBN indicated the generation of a free radical intermediate during the metabolism of phenytoin by PGS. These results suggest that the hydroperoxidase component of PGS, as well as thyroid peroxidase and other peroxidases, can bioactivate phenytoin to a reactive free radical intermediate, which may be toxicologically relevant.
苯妥英的某些毒性作用被认为是由于其经细胞色素P - 450催化生物活化形成一种与蛋白质共价结合的活性芳烃氧化物中间体所致。我们使用体外系统,基于苯妥英被前列腺素合成酶(PGS)、辣根过氧化物酶或甲状腺过氧化物酶共氧化为活性自由基中间体这一情况,研究了另一种假说。将来自肝脏、甲状腺、精囊或肺组织的微粒体,或PGS或辣根过氧化物酶与适当的酶辅因子一起孵育,以研究细胞色素P - 450(NADPH)、PGS(花生四烯酸)、甲状腺过氧化物酶(愈创木酚、H₂O₂)和辣根过氧化物酶(H₂O₂)的活性。通过与微粒体蛋白或牛血清白蛋白共价结合的放射性标记苯妥英的量,以及使用电子自旋共振光谱法检测自由基中间体,来估计体外孵育过程中潜在致畸性的、活性苯妥英中间体的产生。已证明纯化的PGS和公羊精囊(RSV)以及肝脏、肺和肾脏中存在花生四烯酸依赖性的苯妥英生物活化作用。不同组织的最佳花生四烯酸浓度差异很大。通过与环氧化酶抑制剂吲哚美辛共同孵育,苯妥英与PGS和RSV的花生四烯酸依赖性结合降低至基线水平。观察到甲状腺过氧化物酶和辣根过氧化物酶存在过氧化氢依赖性的苯妥英共价结合,并且在这些系统以及PGS和RSV中,通过与过氧化物酶抑制剂甲巯咪唑共同孵育结合显著减少。谷胱甘肽、抗氧化剂咖啡酸和丁基羟基茴香醚以及自由基捕获剂α - 苯基 - N -叔丁基硝酮(PBN)均显著降低了花生四烯酸依赖性的苯妥英结合。PGS对苯妥英的花生四烯酸依赖性生物活化以剂量依赖性方式增加了氧气摄取。使用PBN的电子自旋共振自旋捕获技术表明,PGS代谢苯妥英过程中会产生自由基中间体。这些结果表明,PGS的氢过氧化物酶成分以及甲状腺过氧化物酶和其他过氧化物酶可将苯妥英生物活化成一种活性自由基中间体,这在毒理学上可能具有相关性。