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长期使用利托那韦的时变相互作用:P-糖蛋白和细胞色素 P450 3A 抑制与诱导之间的力量平衡。

Time-dependent interaction of ritonavir in chronic use: the power balance between inhibition and induction of P-glycoprotein and cytochrome P450 3A.

机构信息

Department of Clinical Pharmacokinetics, Faculty of Pharmaceutical Sciences, Kobe Gakuin University, Chuo-ku, Kobe, 650-8586, Japan.

Department of Pharmacokinetics, Kyoto Pharmaceutical University, Yamashina-ku, Kyoto, 607-8412, Japan.

出版信息

J Pharm Sci. 2013 Jun;102(6):2044-2055. doi: 10.1002/jps.23545. Epub 2013 Apr 15.

Abstract

Ritonavir (RTV) is not only an inhibitor but also an immunoreactive inducer of both P-glycoprotein (Pgp) and cytochrome P450 (CYP) 3A in terms of its chronic use. The aim of present study was to test the hypothesis that the power balance between inhibition effects of RTV and induced activities of Pgp and CYP3A depends on the time after last RTV treatment (TimeR) in the chronic use of RTV; rhodamine 123 (Rho) and midazolam (MDZ) were administered at predetermined TimeR to rats pretreated with RTV for 7 days. After oral administration of Rho and MDZ to rats pretreated with RTV for 7 days, the areas under the plasma concentration-time curve of Rho and MDZ were significantly altered depending on TimeR: 1.27-, 0.79-, 0.95-, and 0.11-fold increases over that of the control for Rho at TimeR = 0, 3, 9, and 24 h and 3.12-, 1.50-, 1.27-, and 0.17-fold increases over that of the control for MDZ at TimeR = 0, 3, 9, and 24 h, respectively. These results revealed the presence of the time-dependent interaction of RTV with concomitant drugs in chronic use and should be taken into account in therapeutic strategies for HIV infection.

摘要

利托那韦(RTV)不仅是一种抑制剂,而且是一种慢性使用时具有免疫反应性的 P 糖蛋白(Pgp)和细胞色素 P450(CYP)3A 的诱导剂。本研究的目的是检验以下假设,即在慢性使用 RTV 时,RTV 的抑制作用和 Pgp 和 CYP3A 的诱导活性之间的力量平衡取决于最后一次 RTV 治疗后的时间(TimeR);在 RTV 预处理的大鼠中,在预定的 TimeR 时给予罗丹明 123(Rho)和咪达唑仑(MDZ)。在 RTV 预处理 7 天的大鼠中给予 Rho 和 MDZ 口服后,Rho 和 MDZ 的血浆浓度-时间曲线下面积取决于 TimeR:TimeR = 0、3、9 和 24 h 时 Rho 相对于对照分别增加 1.27、0.79、0.95 和 0.11 倍,TimeR = 0、3、9 和 24 h 时 MDZ 相对于对照分别增加 3.12、1.50、1.27 和 0.17 倍。这些结果揭示了在慢性使用中 RTV 与伴随药物之间存在时间依赖性相互作用,在 HIV 感染的治疗策略中应考虑这一点。

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