Koleva M, Staneva-Stoytcheva D
Institute of Physiology, Bulgarian Academy of Science, Sofia.
Acta Physiol Pharmacol Bulg. 1991;17(2-3):122-8.
Studies were made of the effect of nifedipine on the enzyme-inducing activity of phenobarbital and beta-naphthoflavone estimated by hexobarbital sleeping time, benzphetamine-N-demethylase (BND), ethoxycumarin-O-deethylase (ECOD) and ethoxyresorufin-O-deethylase. (EROD) activity, as well as by the cytochrome P-450 and cytochrome b5 content. Nifedipine at the dose used (100 mg/kg, orally) prolonged hexobarbital sleeping time and affected neither the BND, ECOD and EROD activity, nor the cytochrome P-450 and cytochrome b5 content. On single application nifedipine exerted a different effect on the phenobarbital- or beta-naphthoflavone-provoked enzyme induction. The phenobarbital-induced BND activity and the cytochrome P-450 content were not changed, while the beta-naphthoflavone-induced EROD activity and cytochrome P-450 and cytochrome b5 content decreased, the ECOD activity remaining unchanged. Nifedipine administered for three days significantly increased the BND activity and the cytochrome P-450 content. The three-day administration of nifedipine plus phenobarbital resulted in a further increase in the BND activity and the cytochrome P-450 content. Consistent with this finding was the potentiation of the phenobarbital-induced shortening of hexobarbital sleep. Nifedipine administered at a single dose, one hour before beta-naphthoflavone had no effect per se but potentiated the enzyme-inducing effect of beta-naphthoflavone on the EROD activity and the cytochrome P-450 content but not on the ECOD activity. These data could be taken into account when considering the possible interactions between nifedipine and other drugs applied at different sequence and duration.
研究了硝苯地平对苯巴比妥和β-萘黄酮酶诱导活性的影响,通过己巴比妥睡眠时间、苄非他明-N-脱甲基酶(BND)、乙氧香豆素-O-脱乙基酶(ECOD)和乙氧试卤灵-O-脱乙基酶(EROD)活性以及细胞色素P-450和细胞色素b5含量进行评估。所用剂量(100mg/kg,口服)的硝苯地平延长了己巴比妥睡眠时间,且对BND、ECOD和EROD活性以及细胞色素P-450和细胞色素b5含量均无影响。单次应用时,硝苯地平对苯巴比妥或β-萘黄酮引发的酶诱导有不同影响。苯巴比妥诱导的BND活性和细胞色素P-450含量未改变,而β-萘黄酮诱导的EROD活性以及细胞色素P-450和细胞色素b5含量降低,ECOD活性保持不变。连续三天给予硝苯地平显著增加了BND活性和细胞色素P-450含量。连续三天给予硝苯地平加苯巴比妥导致BND活性和细胞色素P-450含量进一步增加。与此发现一致的是苯巴比妥诱导的己巴比妥睡眠时间缩短增强。在β-萘黄酮给药前一小时单次给予硝苯地平本身无作用,但增强了β-萘黄酮对EROD活性和细胞色素P-450含量的酶诱导作用,而对ECOD活性无影响。在考虑硝苯地平与其他以不同顺序和持续时间应用的药物之间可能的相互作用时,可参考这些数据。