Spracklin D K, Thummel K E, Kharasch E D
Department of Anesthesiology, University of Washington, Seattle 98195, USA.
Drug Metab Dispos. 1996 Sep;24(9):976-83.
The anesthetic halothane undergoes extensive oxidative and reductive biotransformation, resulting in metabolites that cause hepatotoxicity. Halothane is reduced anaerobically by cytochrome P450 (P450) to the volatile metabolites 2-chloro-1,1-difluoroethene (CDE) and 2-chloro-1,1,1-trifluoroethane (CTE). The purpose of this investigation was to identify the human P450 isoform(s) responsible for reductive halothane metabolism. CDE and CTE formation from halothane metabolism by human liver microsomes was determined by GC/MS analysis. Halothane metabolism to CDE and CTE under reductive conditions was completely inhibited by carbon monoxide, which implicates exclusively P450 in this reaction. Eadie-Hofstee plots of both CDE and CTE formation were nonlinear, suggesting multiple P450 isoform involvement. Microsomal CDE and CTE formation were each inhibited 40-50% by P450 2A6-selective inhibitors (coumarin and 8-methoxypsoralen) and 55-60% by P450 3A4-selective inhibitors (ketoconazole and troleandomycin). P450 1A-, 2B6-, 2C9/10-, and 2D6-selective inhibitors (7,8-benzoflavone, furafylline, orphenadrine, sulfaphenazole, and quinidine) had no significant effect on reductive halothane metabolism. Measurement of product formation catalyzed by a panel of cDNA-expressed P450 isoforms revealed that maximal rates of CDE formation occurred with P450 2A6, followed by P450 3A4. P450 3A4 was the most effective catalyst of CTE formation. Among a panel of 11 different human livers, there were significant linear correlations between the rate of CDE formation and both 2A6 activity (r = 0.64, p < 0.04) and 3A4 activity (r = 0.64, p < 0.03). Similarly, there were significant linear correlations between CTE formation and both 2A6 activity (r = 0.55, p < 0.08) and 3A4 activity (r = 0.77, p < 0.005). The P450 2E1 inhibitors 4-methylpyrazole and diethyldithiocarbamate inhibited CDE and CTE formation by 20-45% and 40-50%, respectively; however, cDNA-expressed P450 2E1 did not catalyze significant amounts of CDE or CTE production, and microsomal metabolite formation was not correlated with P450 2E1 activity. This investigation demonstrated that human liver microsomal reductive halothane metabolism is catalyzed predominantly by P450 2A6 and 3A4. This isoform selectivity for anaerobic halothane metabolism contrasts with that for oxidative human halothane metabolism, which is catalyzed predominantly by P450 2E1.
麻醉药氟烷会经历广泛的氧化和还原生物转化,产生具有肝毒性的代谢产物。氟烷在细胞色素P450(P450)的作用下进行厌氧还原,生成挥发性代谢产物2-氯-1,1-二氟乙烯(CDE)和2-氯-1,1,1-三氟乙烷(CTE)。本研究的目的是确定负责氟烷还原代谢的人P450同工酶。通过气相色谱/质谱分析测定人肝微粒体中氟烷代谢生成CDE和CTE的情况。在还原条件下,氟烷代谢生成CDE和CTE的过程被一氧化碳完全抑制,这表明该反应仅涉及P450。CDE和CTE生成的伊迪-霍夫斯蒂图均呈非线性,提示有多种P450同工酶参与。P450 2A6选择性抑制剂(香豆素和8-甲氧基补骨脂素)和P450 3A4选择性抑制剂(酮康唑和醋竹桃霉素)分别使微粒体CDE和CTE生成量抑制40 - 50%和55 - 60%。P450 1A、2B6、2C9/10和2D6选择性抑制剂(7,8-苯并黄酮、呋拉茶碱、苯海拉明、磺胺苯吡唑和奎尼丁)对氟烷还原代谢无显著影响。对一组cDNA表达的P450同工酶催化产物生成的测定表明,P450 2A6催化CDE生成的速率最高,其次是P450 3A4。P450 3A4是CTE生成的最有效催化剂。在11个不同的人肝脏样本中,CDE生成速率与2A6活性(r = 0.64,p < 0.04)和3A4活性(r = 0.64,p < 0.03)之间均存在显著的线性相关性。同样,CTE生成与2A6活性(r = 0.55,p < 0.08)和3A4活性(r = 0.77,p < 0.005)之间也存在显著的线性相关性。P450 2E1抑制剂4-甲基吡唑和二乙基二硫代氨基甲酸盐分别使CDE和CTE生成量抑制20 - 45%和40 - 50%;然而,cDNA表达的P450 2E1并未催化生成大量的CDE或CTE,且微粒体代谢产物生成与P450 2E1活性无关。本研究表明,人肝微粒体氟烷还原代谢主要由P450 2A6和3A4催化。这种对厌氧氟烷代谢的同工酶选择性与氧化型人氟烷代谢不同,后者主要由P450 2E1催化。