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酶诱导药物组合及其对人体肝脏微粒体酶活性的影响。

Enzyme-inducing drug combinations and their effects on liver microsomal enzyme activity in man.

作者信息

Ohnhaus E E, Gerber-Taras E, Park B K

出版信息

Eur J Clin Pharmacol. 1983;24(2):247-50. doi: 10.1007/BF00613826.

Abstract

The effect of 2 different drug combinations on liver microsomal activity was investigated in healthy volunteers by administering antipyrine 1200 mg and phenobarbitone 100 mg, or the same dose of antipyrine with rifampicin 600 mg daily for 14 days. The effect of rifampicin 1200 mg given for only 8 days was also studied. Before and after each drug regimen, estimates were made of the total body clearance of antipyrine, gamma-glutamyl-transferase (gamma-GT) and urinary excretion of 6-beta-hydroxycortisol as in vivo parameters of liver microsomal enzyme activity. Following combined antipyrine and phenobarbitone administration, the antipyrine clearance was increased by 80%, after antipyrine with rifampicin by 128%, and after rifampicin alone by 104%. 6-beta-hydroxycortisol, corrected for 17-hydroxycorticosteroids, increased from 2.6% to 8% following antipyrine plus phenobarbitone, from 4.4% to 27.9% following antipyrine plus rifampicin, and from 5.4% to 29.7% after rifampicin given alone. Based on previous studies, antipyrine given with phenobarbitone produced slightly more induction than phenobarbitone given alone. Following antipyrine 1200 mg with rifampicin 600 mg for 14 days a significantly greater increase in antipyrine clearance and 6-beta-hydroxycortisol excretion was observed than when either drug was given alone.

摘要

通过给健康志愿者服用1200毫克安替比林和100毫克苯巴比妥,或相同剂量的安替比林与600毫克利福平,每日一次,共14天,研究了两种不同药物组合对肝脏微粒体活性的影响。还研究了仅服用8天1200毫克利福平的效果。在每种药物治疗方案前后,对安替比林的全身清除率、γ-谷氨酰转移酶(γ-GT)以及6-β-羟基皮质醇的尿排泄进行了评估,作为肝脏微粒体酶活性的体内参数。联合服用安替比林和苯巴比妥后,安替比林清除率增加了80%,安替比林与利福平联合服用后增加了128%,单独服用利福平后增加了104%。校正17-羟基皮质类固醇后,6-β-羟基皮质醇在安替比林加苯巴比妥后从2.6%增至8%,安替比林加利福平后从4.4%增至27.9%,单独服用利福平后从5.4%增至29.7%。根据先前的研究,安替比林与苯巴比妥联合使用产生的诱导作用略大于单独使用苯巴比妥。在服用1200毫克安替比林和600毫克利福平14天后,观察到安替比林清除率和6-β-羟基皮质醇排泄的增加显著大于单独使用任何一种药物时。

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