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涉及奥司他韦和中药的药代动力学和药效学相互作用的从实验室到病床的证据。

Bench to bed evidences for pharmacokinetic and pharmacodynamic interactions involving oseltamivir and chinese medicine.

机构信息

Institute of Medicinal Plant Development, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100193, China ; School of Pharmacy, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.

School of Pharmacy, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.

出版信息

Evid Based Complement Alternat Med. 2014;2014:354172. doi: 10.1155/2014/354172. Epub 2014 Jan 9.

Abstract

Oseltamivir (OA), an ethyl ester prodrug of oseltamivir carboxylate (OC), is clinically used as a potent and selective inhibitor of neuraminidase. Chinese medicines have been advocated to combine with conventional drug for avian influenza. The current study aims to investigate the potential pharmacokinetic and pharmacodynamic interactions of a Chinese medicine formula, namely, Yin Qiao San and Sang Ju Yin (CMF1), commonly used for anti-influenza in combination with OA in both rat and human, and to reveal the underlined mechanisms. It was found that although C max, AUC and urinary recovery of OC, as well as metabolic ratio (AUCOC/AUCOA), were significantly decreased in a dose-dependent manner following combination use of CMF1 and OA in rat studies (P < 0.01), such coadministration in 14 healthy volunteers only resulted in a trend of minor decrease in the related parameters. Further mechanistic studies found that although CMF1 could reduce absorption and metabolism of OA, it appears to enhance viral inhibition of OA (P < 0.01). In summary, although there was potential interaction between OA and CMF1 found in rat studies, its clinical impact was expected to be minimal. The coadministration of OA and CMF1 at the clinical recommended dosages is, therefore, considered to be safe.

摘要

奥司他韦(OA)是奥司他韦羧酸(OC)的乙酯前药,临床上用作神经氨酸酶的有效且选择性抑制剂。中药被提倡与常规药物联合用于治疗禽流感。本研究旨在探讨中药配方银桥散和桑菊饮(CMF1)与 OA 联合使用在大鼠和人体中的潜在药代动力学和药效学相互作用,并揭示其潜在机制。研究发现,虽然在大鼠研究中,CMF1 与 OA 联合使用时,OC 的 C max、AUC 和尿回收率以及代谢比(AUCOC/AUCOA)均呈剂量依赖性显著降低(P<0.01),但在 14 名健康志愿者中的联合使用仅显示出相关参数略有降低的趋势。进一步的机制研究发现,虽然 CMF1 可以降低 OA 的吸收和代谢,但似乎增强了 OA 的病毒抑制作用(P<0.01)。综上所述,虽然在大鼠研究中发现 OA 与 CMF1 之间存在潜在的相互作用,但预计其临床影响很小。因此,在临床推荐剂量下,OA 和 CMF1 的联合使用被认为是安全的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e495/3912631/9f4808a6d180/ECAM2014-354172.001.jpg

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