Teschke R, Matsuzaki S, Ohnishi K, Hasumura Y, Lieber C S
Adv Exp Med Biol. 1977;85A:257-80. doi: 10.1007/978-1-4899-5181-6_18.
At intermediate and higher alcohol concentrations, ethanol metabolism proceeds via alcohol dehydrogenase (ADH) and the microsomal ethanol oxidizing system (MEOS), whereas catalase plays no significant role. Following prolonged ethanol consumption, an enhancement of both MEOS activity as well as the rates of ethanol metabolism occurs; the latter persisted despite inhibition of ADH by pyrazole and catalase by sodium axide, suggesting the involvement of MEOS in the adaptive increase. MEOS exhibits characteristics similar to those of other microsomal drug metabolizing enzymes and can be differentiated and isolated from both ADH and catalase activities. Reconstitution of MEOS activity was achieved with partially purified cytochrome P-450 and NADPH-cytochrome c reductase in the presence of synthetic phospholipid.
在中等及更高酒精浓度下,乙醇代谢通过乙醇脱氢酶(ADH)和微粒体乙醇氧化系统(MEOS)进行,而过氧化氢酶不起重要作用。长期摄入乙醇后,MEOS活性以及乙醇代谢速率均增强;尽管吡唑抑制ADH且氧化钠抑制过氧化氢酶,但后者仍持续存在,这表明MEOS参与了适应性增加。MEOS表现出与其他微粒体药物代谢酶相似的特性,并且可以与ADH和过氧化氢酶活性区分开来并进行分离。在合成磷脂存在的情况下,用部分纯化的细胞色素P-450和NADPH-细胞色素c还原酶实现了MEOS活性的重建。