Subramanyam B, Pond S M, Eyles D W, Whiteford H A, Fouda H G, Castagnoli N
Department of Chemistry, Virginia Polytechnic Institute and State University, Blacksburg 24061-0212.
Biochem Biophys Res Commun. 1991 Dec 16;181(2):573-8. doi: 10.1016/0006-291x(91)91228-5.
Evidence that the parkinsonian inducing agent MPTP is biotransformed to a pyridinium species that selectively destroys nigrostriatal neurons in humans and subhuman primates has prompted studies to evaluate the metabolic fate of the structurally related neuroleptic agent haloperidol. With the aid of a highly sophisticated atmospheric pressure ionspray HPLC/MS/MS assay, unambiguous evidence has been obtained for the presence of the haloperidol pyridinium species in extracts of urine obtained from haloperidol-treated patients and in extracts of NADPH-supplemented human liver microsomal incubation mixtures containing haloperidol. The potential significance of the formation of this putative neurotoxic pyridinium species is considered.
有证据表明,帕金森病诱发剂MPTP可生物转化为一种吡啶鎓物质,该物质能选择性地破坏人类和非人灵长类动物的黑质纹状体神经元,这促使人们开展研究以评估结构相关的抗精神病药物氟哌啶醇的代谢命运。借助一种高度精密的常压离子喷雾HPLC/MS/MS测定法,已获得明确证据,证明在氟哌啶醇治疗患者的尿液提取物以及含有氟哌啶醇的补充NADPH的人肝微粒体孵育混合物提取物中存在氟哌啶醇吡啶鎓物质。文中考虑了这种假定的神经毒性吡啶鎓物质形成的潜在意义。