Departments of Biochemistry and Molecular Biology (M.A.S, G.P.M.) and Environmental and Occupational Health (G.B.), University of Arkansas for Medical Sciences, Little Rock, Arizona (M.A.S.); Department of Pathology and Immunology, Washington University, St. Louis, Missouri (N.R.F., S.J.S.); Department of Chemistry, Hendrix College, Conway, Arizona (S.P.); and Independent Researcher (B.M.S.) and Department of Chemistry and Biochemistry (A.O.P., D.W.P.), Harding University, Searcy, Arkansas.
Departments of Biochemistry and Molecular Biology (M.A.S, G.P.M.) and Environmental and Occupational Health (G.B.), University of Arkansas for Medical Sciences, Little Rock, Arizona (M.A.S.); Department of Pathology and Immunology, Washington University, St. Louis, Missouri (N.R.F., S.J.S.); Department of Chemistry, Hendrix College, Conway, Arizona (S.P.); and Independent Researcher (B.M.S.) and Department of Chemistry and Biochemistry (A.O.P., D.W.P.), Harding University, Searcy, Arkansas
Drug Metab Dispos. 2021 Feb;49(2):133-141. doi: 10.1124/dmd.120.000254. Epub 2020 Nov 25.
Meclofenamate is a nonsteroidal anti-inflammatory drug used in the treatment of mild-to-moderate pain yet poses a rare risk of hepatotoxicity through an unknown mechanism. Nonsteroidal anti-inflammatory drug (NSAID) bioactivation is a common molecular initiating event for hepatotoxicity. Thus, we hypothesized a similar mechanism for meclofenamate and leveraged computational and experimental approaches to identify and characterize its bioactivation. Analyses employing our XenoNet model indicated possible pathways to meclofenamate bioactivation into 19 reactive metabolites subsequently trapped into glutathione adducts. We describe the first reported bioactivation kinetics for meclofenamate and relative importance of those pathways using human liver microsomes. The findings validated only four of the many bioactivation pathways predicted by modeling. For experimental studies, dansyl glutathione was a critical trap for reactive quinone metabolites and provided a way to characterize adduct structures by mass spectrometry and quantitate yields during reactions. Of the four quinone adducts, we were able to characterize structures for three of them. Based on kinetics, the most efficient bioactivation pathway led to the monohydroxy para-quinone-imine followed by the dechloro-ortho-quinone-imine. Two very inefficient pathways led to the dihydroxy ortho-quinone and a likely multiply adducted quinone. When taken together, bioactivation pathways for meclofenamate accounted for approximately 13% of total metabolism. In sum, XenoNet facilitated prediction of reactive metabolite structures, whereas quantitative experimental studies provided a tractable approach to validate actual bioactivation pathways for meclofenamate. Our results provide a foundation for assessing reactive metabolite load more accurately for future comparative studies with other NSAIDs and drugs in general. SIGNIFICANCE STATEMENT: Meclofenamate bioactivation may initiate hepatotoxicity, yet common risk assessment approaches are often cumbersome and inefficient and yield qualitative insights that do not scale relative bioactivation risks. We developed and applied innovative computational modeling and quantitative kinetics to identify and validate meclofenamate bioactivation pathways and relevance as a function of time and concentration. This strategy yielded novel insights on meclofenamate bioactivation and provides a tractable approach to more accurately and efficiently assess other drug bioactivations and correlate risks to toxicological outcomes.
甲氯芬那酸是一种非甾体抗炎药,用于治疗轻至中度疼痛,但通过未知机制存在罕见的肝毒性风险。非甾体抗炎药 (NSAID) 的生物活化是肝毒性的常见分子起始事件。因此,我们假设甲氯芬那酸存在类似的机制,并利用计算和实验方法来识别和表征其生物活化。利用我们的 XenoNet 模型进行的分析表明,甲氯芬那酸可能的生物活化途径将其转化为 19 种反应性代谢物,随后这些代谢物与谷胱甘肽结合物结合。我们描述了甲氯芬那酸生物活化动力学的首次报道,并使用人肝微粒体研究了这些途径的相对重要性。研究结果仅验证了建模预测的许多生物活化途径中的四种。对于实验研究,Dansyl 谷胱甘肽是反应性醌代谢物的关键捕获剂,并通过质谱法提供了一种在反应过程中表征加合物结构和定量产率的方法。在所研究的四种醌加合物中,我们能够对其中三种的结构进行表征。基于动力学,最有效的生物活化途径导致单羟基对醌亚胺,其次是去氯邻醌亚胺。两种非常低效的途径导致二羟基邻醌和可能的多取代醌。总的来说,甲氯芬那酸的生物活化途径约占总代谢的 13%。总之,XenoNet 促进了反应性代谢物结构的预测,而定量实验研究为验证甲氯芬那酸的实际生物活化途径提供了一种可行的方法。我们的研究结果为更准确地评估未来与其他 NSAIDs 和一般药物的比较研究中的反应性代谢物负荷提供了基础。意义声明:甲氯芬那酸的生物活化可能引发肝毒性,但常见的风险评估方法通常繁琐且效率低下,并且产生的定性见解不能按比例反映相对生物活化风险。我们开发并应用了创新的计算建模和定量动力学方法来识别和验证甲氯芬那酸的生物活化途径及其作为时间和浓度函数的相关性。这种策略为甲氯芬那酸的生物活化提供了新的见解,并为更准确和有效地评估其他药物的生物活化以及将风险与毒理学结果相关联提供了一种可行的方法。