Barry M, Howe J, Back D, Breckenridge A, Brettle R, Mitchell R, Beeching N J, Nye F J
Department of Pharmacology and Therapeutics, University of Liverpool.
Br J Clin Pharmacol. 1993 Jul;36(1):82-5. doi: 10.1111/j.1365-2125.1993.tb05898.x.
The effects of indomethacin and naproxen on zidovudine (ZDV) pharmacokinetics were studied in six patients with the acquired immunodeficiency syndrome (AIDS), AIDS related complex (ARC) or asymptomatic HIV disease using a placebo-controlled crossover design. Indomethacin 25 mg twice daily or naproxen 250 mg twice daily did not alter ZDV pharmacokinetics compared with placebo. The mean AUC value for the glucuronidated metabolite, GZDV, was reduced from 26.6 +/- 11.7 mumol l-1 h in the presence of placebo to 20.9 +/- 8.3 mumol l-1 h (95% C.I. of the difference 1.39-9.98; P < 0.05) following treatment with naproxen 250 mg twice daily for 3 days. The small decrease in plasma GZDV in the naproxen phase reflects an increase in clearance of ZDV to other metabolites and/or a decrease in the formation clearance to GZDV and/or an increase in the clearance of GZDV. A decrease in formation clearance to GZDV would be consistent with the results of in vitro studies reported previously. No significant increase in ZDV concentration in the presence of naproxen may reflect a lower sensitivity of parent drug measurements to selective inhibition of parallel pathways of metabolism. The clinical significance of these findings is unknown but toxicity may be increased if a decreased formation of GZDV is accompanied by shunting of metabolism to 3'-amino-3'-deoxythymidine which is alleged to be cytotoxic.
采用安慰剂对照交叉设计,在6例获得性免疫缺陷综合征(AIDS)、AIDS相关综合征(ARC)或无症状HIV疾病患者中研究了吲哚美辛和萘普生对齐多夫定(ZDV)药代动力学的影响。与安慰剂相比,每日两次服用25mg吲哚美辛或每日两次服用250mg萘普生均未改变ZDV的药代动力学。葡萄糖醛酸化代谢产物GZDV的平均AUC值,在服用安慰剂时为26.6±11.7μmol·l-1·h,在每日两次服用250mg萘普生治疗3天后降至20.9±8.3μmol·l-1·h(差异的95%置信区间为1.39 - 9.98;P<0.05)。萘普生治疗阶段血浆GZDV的小幅下降反映了ZDV向其他代谢产物的清除增加和/或向GZDV的生成清除减少和/或GZDV的清除增加。向GZDV的生成清除减少与先前报道的体外研究结果一致。萘普生存在时ZDV浓度无显著增加可能反映了母体药物测量对代谢平行途径选择性抑制的敏感性较低。这些发现的临床意义尚不清楚,但如果GZDV生成减少伴随着代谢转向据称具有细胞毒性的3'-氨基-3'-脱氧胸苷,毒性可能会增加。