Ranitidine Increases Bioavailability of Acetaminophen by Inhibiting First‐Pass Glucuronidation in Man

H. Itoh, T. Nagano, Tetsuji Hayashi, M. Takeyama
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引用次数: 8

Abstract

The effect of the histamine H2 receptor antagonist, ranitidine, on plasma concentrations of acetaminophen was investigated with respect to hepatic metabolism, in five volunteers. Acetaminophen (1000 mg) together with ranitidine (300 mg), placebo or at 1 h after ranitidine (300 mg) was orally administered to five healthy male volunteers. Venous blood samples were taken before and after drug administration. Plasma acetaminophen and acetaminophen conjugates (glucuronide and sulphate) were determined by HPLC. The pharmacokinetic parameters were calculated from the plasma acetaminophen concentration-time curves from each volunteer. The area under the plasma acetaminophen concentration-time curve from 0 to 3 h (AUC0–3) significantly (P < 0.01) increased from 13.03 ± 0.84 μg h mL−1 (placebo coadministration) to 21.30 ± 0.60 μg h mL−1 (ranitidine coadministration). The peak plasma acetaminophen concentration significantly (P < 0.01) increased from 18.30 ± 2.26 μg mL−1 (placebo coadministration) to 34.14 ± 1.07 μg mL−1 (ranitidine coadministration) 30 min after administration. Plasma acetaminophen concentrations with ranitidine were significantly increased at 15 to 120 min compared with placebo. Plasma acetaminophen glucuronide conjugate concentrations with ranitidine were significantly decreased at 15 to 45 min compared with placebo, whereas plasma acetaminophen sulphate conjugate concentrations were not significantly altered. Plasma acetaminophen and acetaminophen conjugate concentrations were not significantly different between placebo-coadministration and in the case where acetaminophen was orally administered 1 h after ranitidine. Coadministration of acetaminophen and ranitidine reduced plasma acetaminophen glucuronide concentrations and significantly increased plasma acetaminophen concentrations. The effects of ranitidine are as a result of the prevention of first-pass hepatic metabolism, by prevention of acetaminophen glucuronyltransferase. Thus care must be taken when acetaminophen and ranitidine are coadministered.
雷尼替丁通过抑制人体第一次葡萄糖醛酸化提高对乙酰氨基酚的生物利用度
在5名志愿者中,研究了组胺H2受体拮抗剂雷尼替丁对对乙酰氨基酚血浆浓度的影响。对乙酰氨基酚(1000毫克)与雷尼替丁(300毫克)、安慰剂或在雷尼替丁(300毫克)后1小时口服给5名健康男性志愿者。给药前后分别取静脉血。用高效液相色谱法测定血浆中对乙酰氨基酚和对乙酰氨基酚偶联物(葡萄糖醛酸盐和硫酸盐)的含量。根据每位志愿者的血浆对乙酰氨基酚浓度-时间曲线计算药代动力学参数。0 ~ 3 h血浆对乙酰氨基酚浓度-时间曲线下面积(AUC0-3)由安慰剂组(13.03±0.84 μg h mL−1)显著增加至雷尼替丁组(21.30±0.60 μg h mL−1)(P < 0.01)。给药后30min对乙酰氨基酚峰浓度由安慰剂组18.30±2.26 μg mL−1升高至雷尼替丁组34.14±1.07 μg mL−1,差异有统计学意义(P < 0.01)。与安慰剂组相比,雷尼替丁组在15 ~ 120分钟时血浆对乙酰氨基酚浓度显著升高。与安慰剂相比,血浆对乙酰氨基酚葡萄糖醛酸盐与雷尼替丁结合的浓度在15至45分钟显著降低,而血浆对乙酰氨基酚硫酸盐结合的浓度没有显著改变。对乙酰氨基酚和对乙酰氨基酚偶联物的血浆浓度在安慰剂联合给药和在雷尼替丁后1小时口服对乙酰氨基酚的情况下没有显著差异。对乙酰氨基酚和雷尼替丁联合用药可降低血浆对乙酰氨基酚葡萄糖醛酸盐浓度,并显著增加血浆对乙酰氨基酚浓度。雷尼替丁的作用是通过预防对乙酰氨基酚葡萄糖醛酸转移酶来预防首过肝脏代谢。因此,当对乙酰氨基酚和雷尼替丁同时使用时,必须小心。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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