Morita K, Shibata H, Ono T, Shimakawa H
Eur J Clin Pharmacol. 1986;31(1):117-8. doi: 10.1007/BF00870999.
The inducing effect of feprazone, a pyrazolone anti-inflammatory agent, on hepatic drug-metabolizing enzymes has been studied in healthy volunteers. The ratio of 6 beta-hydroxycortisol (6 beta-OHF) to 17-hydroxycorticosteroids (17-OHCS) in urine, used as an indicator of oxidative drug-metabolizing enzyme activity, was increased up to 1.6-times the original level after 5 days of oral treatment with feprazone 300 mg/day. This indicates that feprazone induces hepatic drug-metabolising enzymes in man as does phenylbutazone.
吡唑酮类抗炎药非普拉宗对肝药酶的诱导作用已在健康志愿者中进行了研究。尿中6β-羟基皮质醇(6β-OHF)与17-羟基皮质类固醇(17-OHCS)的比值用作氧化药物代谢酶活性的指标,在每天口服300mg非普拉宗治疗5天后,该比值增加至原来水平的1.6倍。这表明非普拉宗在人体内诱导肝药酶的作用与保泰松相同。