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口服避孕药类固醇对苯二氮䓬类药物代谢的不同影响。

Differential effects of oral contraceptive steroids on the metabolism of benzodiazepines.

作者信息

Patwardhan R V, Mitchell M C, Johnson R F, Schenker S

出版信息

Hepatology. 1983 Mar-Apr;3(2):248-53. doi: 10.1002/hep.1840030219.

Abstract

The effects of oral contraceptive steroids (OCS) on the disposition and elimination of lorazepam, oxazepam, and chlordiazepoxide were examined. Lorazepam and oxazepam are metabolized via glucuronidation while chlordiazepoxide is metabolized by oxidation in the liver. The disposition and elimination of lorazepam, oxazepam, and chlordiazepoxide was studied in females not taking OCS and females taking OCS (norethindrone acetate, 1 mg; ethinyl estradiol, 50 micrograms) for 6 months or more. The t1/2 (beta) for lorazepam was significantly reduced in women taking OCS (6.0 +/- 3.1 vs. 14.0 +/- 6.2 hr) (p less than 0.005) as compared to controls, and the t1/2 (beta) for oxazepam was reduced in women taking OCS (7.71 +/- 3.23 vs. 12.09 +/- 5.08 hr) as compared to controls, but did not reach statistical significance. The plasma clearance of both lorazepam and oxazepam was significantly increased in women taking OCS [(288.9 +/- 165.9 vs. 77.5 +/- 3.29 ml per min) (p less than 0.01) and (251.2 +/- 106.9 vs. 97.86 +/- 69.4 ml per min) (p less than 0.01), respectively] as compared to controls. The volumes of distribution of lorazepam and oxazepam were significantly increased in women taking OCS (p less than 0.05) while plasma binding of these drugs was similar in both groups. In contrast, the t1/2 (beta) of chlordiazepoxide was significantly prolonged (20.58 +/- 8.08 vs. 11.63 +/- 5.91 hr) (p less than 0.05), and the plasma clearance was significantly reduced (13.41 +/- 4.69 vs. 33.22 +/- 12.37 ml per min) (p less than 0.05) in the OCS group as compared to controls. The volumes of distribution of chlordiazepoxide were similar in both groups, and the plasma binding of chlordiazepoxide tended to be lower in the OCS group but did not reach statistical significance. We conclude that OCS exert a differential effect on the elimination of benzodiazepines, whereby oxidation of chlordiazepoxide is impaired while the glucuronidation of lorazepam and oxazepam is enhanced by OCS.

摘要

研究了口服避孕药类固醇(OCS)对劳拉西泮、奥沙西泮和氯氮卓的处置及消除的影响。劳拉西泮和奥沙西泮通过葡萄糖醛酸化代谢,而氯氮卓在肝脏中通过氧化代谢。在未服用OCS的女性和服用OCS(醋酸炔诺酮1毫克;炔雌醇50微克)6个月或更长时间的女性中研究了劳拉西泮、奥沙西泮和氯氮卓的处置及消除情况。与对照组相比,服用OCS的女性中劳拉西泮的t1/2(β)显著缩短(6.0±3.1小时对14.0±6.2小时)(p<0.005),服用OCS的女性中奥沙西泮的t1/2(β)缩短(7.71±3.23小时对12.09±5.08小时),但未达到统计学显著性。与对照组相比,服用OCS的女性中劳拉西泮和奥沙西泮的血浆清除率均显著增加[分别为(288.9±165.9对77.5±3.29毫升/分钟)(p<0.01)和(251.2±106.9对97.86±69.4毫升/分钟)(p<0.01)]。服用OCS的女性中劳拉西泮和奥沙西泮的分布容积显著增加(p<0.05),而两组中这些药物的血浆蛋白结合率相似。相比之下,与对照组相比,OCS组中氯氮卓的t1/2(β)显著延长(20.58±8.08小时对11.63±5.91小时)(p<0.05),血浆清除率显著降低(13.41±4.69对33.22±12.37毫升/分钟)(p<0.05)。两组中氯氮卓的分布容积相似,OCS组中氯氮卓的血浆蛋白结合率倾向于较低,但未达到统计学显著性。我们得出结论,OCS对苯二氮䓬类药物的消除有不同影响,即OCS损害氯氮卓的氧化,而增强劳拉西泮和奥沙西泮的葡萄糖醛酸化。

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