Lucas D, Berthou F, Dréano Y, Lozac'h P, Volant A, Ménez J F
Faculté de Médecine, Laboratoire de Biochimie, Brest, France.
Alcohol Clin Exp Res. 1993 Aug;17(4):900-5. doi: 10.1111/j.1530-0277.1993.tb00861.x.
Hepatic microsomal cytochromes P-450 CYP1A2, and CYP2E1 contents and catalytic activities have been simultaneously investigated in 42 patients undergoing diagnostic liver biopsy. CYP1A2 contents, measured by Western blotting, were correlated with methoxyresorufin-O-demethylation and ethoxyresorufin-O-deethylation (r = 0.65 and r = 0.66, p < 0.001, respectively). CYP2E1 contents were correlated with 1-butanol oxidation and 6-hydroxylation of chlorzoxazone (r = 0.75 for both, p < 0.001). CYP1A2 catalytic activities varied by 30- to 40-fold, whereas CYP2E1 activities varied by 6- to 20-fold. In our study, these variations were not related to liver diseases or cancer of the digestive tract nor to alcohol drinking or smoking habits, because patients were alcohol- and tobacco-free for 1 month before the study. Other environmental factors, diet habits, and/or genetic factors could explain the large interindividual variations observed.
在42例接受诊断性肝活检的患者中,同时研究了肝微粒体细胞色素P-450 CYP1A2和CYP2E1的含量及催化活性。通过蛋白质免疫印迹法测定的CYP1A2含量与甲氧基试卤灵-O-脱甲基化及乙氧基试卤灵-O-脱乙基化相关(r分别为0.65和0.66,p均<0.001)。CYP2E1含量与1-丁醇氧化及氯唑沙宗的6-羟基化相关(两者r均为0.75,p<0.001)。CYP1A2的催化活性变化范围为30至40倍,而CYP2E1的活性变化范围为6至20倍。在我们的研究中,这些变化与肝脏疾病或消化道癌症无关,也与饮酒或吸烟习惯无关,因为患者在研究前1个月未饮酒和吸烟。其他环境因素、饮食习惯和/或遗传因素可能解释所观察到的个体间的巨大差异。