Teunissen M W, Bakker W, Meerburg-Van der Torren J E, Breimer D D
Br J Clin Pharmacol. 1984 Nov;18(5):701-6. doi: 10.1111/j.1365-2125.1984.tb02532.x.
The influence of an 8-day therapy with rifampicin (600 mg daily) was studied on antipyrine plasma clearance and metabolite formation in seven patients with tuberculosis (age 18-79 years), who were also treated with isoniazid and pyrazinamide. After rifampicin treatment the elimination half-life of antipyrine had decreased in all patients from 12.9 +/- 5.0 to 8.8 +/- 2.0 h (P less than 0.05). Antipyrine clearance had increased from 2.2 +/- 0.9 to 2.9 +/- 0.7 l/h (P less than 0.05), while no change in apparent volume of distribution was observed. The increase in antipyrine clearance was primarily due to a selective increase in the rate of formation of norantipyrine by 80% from 6.9 +/- 3.4 to 12.4 +/- 3.4 ml/min. Rifampicin seems to induce preferentially the cytochrome P-450 (iso-) enzyme(s) involved in the demethylation of antipyrine to norantipyrine. Other pathways of antipyrine metabolism were hardly affected. This provides further evidence for the involvement of different iso-enzymes of the cytochrome P-450 system in antipyrine metabolism in man.
研究了利福平(每日600毫克)8天疗法对7例结核病患者(年龄18 - 79岁)安替比林血浆清除率及代谢物形成的影响,这些患者同时接受异烟肼和吡嗪酰胺治疗。利福平治疗后,所有患者安替比林的消除半衰期从12.9±5.0小时降至8.8±2.0小时(P<0.05)。安替比林清除率从2.2±0.9升/小时增至2.9±0.7升/小时(P<0.05),而分布容积未见变化。安替比林清除率的增加主要是由于去甲安替比林生成速率选择性增加80%,从6.9±3.4毫升/分钟增至12.4±3.4毫升/分钟。利福平似乎优先诱导参与安替比林脱甲基生成去甲安替比林的细胞色素P - 450(同工)酶。安替比林代谢的其他途径几乎未受影响。这为细胞色素P - 450系统的不同同工酶参与人体安替比林代谢提供了进一步证据。