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芪参益气滴丸通过抑制大鼠 Mrp2 表达增加阿托伐他汀生物利用度。

QiShenYiQi pills, a Chinese patent medicine, increase bioavailability of atorvastatin by inhibiting Mrp2 expression in rats.

机构信息

National Clinical Drug Monitoring Center, Hebei General Hospital, Shijiazhuang, China.

Department of Pharmacy, The Second Hospital of Shijiazhuang, Shijiazhuang, China.

出版信息

Pharm Biol. 2022 Dec;60(1):185-194. doi: 10.1080/13880209.2021.2021949.

Abstract

CONTEXT

Atorvastatin (ATV) and QiShenYiQi pills (QSYQ), a Chinese patent medicine, are often co-prescribed to Chinese cardiovascular patients. The effects of QSYQ on the pharmacokinetics of ATV have not been studied.

OBJECTIVE

We investigated the influence of QSYQ on the pharmacokinetics of ATV and its metabolites upon oral or intravenous administration of ATV to rats.

MATERIALS AND METHODS

Sprague-Dawley rats ( = 5/group) were pre-treated with oral QSYQ (675 mg/kg) or vehicle control for 7 days and then orally administrated ATV (10 mg/kg) or intravenously administrated ATV (2 mg/kg). Serum concentrations of ATV and metabolites were determined by ultra-high performance liquid chromatography tandem mass spectrometry. Expression of metabolic enzymes and transporters in jejunum and ileum were measured by quantitative real-time PCR and Western blot.

RESULTS

QSYQ resulted in an increase of AUC of ATV from 226.67 ± 42.11 to 408.70 ± 161.75 ng/mL/h and of of ATV from 101.46 ± 26.18 to 198.00 ± 51.69 ng/mL and in an increased of hydroxy atorvastatin from 9.07 ± 6.20 to 23.10 ± 8.70 ng/mL in rats administered ATV orally. No change was observed in rats treated intravenously. The expression of multidrug resistance-associated protein 2 mRNA and protein decreased in ileum, and the mRNA of P-glycoprotein decreased in jejunum, though no change in protein expression was found.

DISCUSSION AND CONCLUSIONS

QSYQ increased bioavailability of ATV administered orally through inhibiting the expression of Mrp2 in ileum. Clinicians should pay close attention to potential drug-drug interactions between ATV and QSYQ.

摘要

背景

阿托伐他汀(ATV)和芪参益气滴丸(QSYQ),一种中药专利药,常被同时用于中国心血管病患者。QSYQ 对 ATV 药代动力学的影响尚未研究。

目的

我们研究了 QSYQ 对 ATV 及其代谢物在大鼠口服或静脉给予 ATV 时药代动力学的影响。

材料和方法

Sprague-Dawley 大鼠(每组 5 只)预先用口服 QSYQ(675mg/kg)或载体对照处理 7 天,然后口服给予 ATV(10mg/kg)或静脉内给予 ATV(2mg/kg)。通过超高效液相色谱串联质谱法测定血清中 ATV 和代谢物的浓度。采用实时定量 PCR 和 Western blot 法测定空肠和回肠中代谢酶和转运体的表达。

结果

QSYQ 使口服给予 ATV 的 AUC 从 226.67±42.11ng/mL/h 增加至 408.70±161.75ng/mL/h,使 从 101.46±26.18ng/mL 增加至 198.00±51.69ng/mL,并使口服给予 ATV 的羟基阿托伐他汀从 9.07±6.20ng/mL 增加至 23.10±8.70ng/mL。静脉内给予 ATV 的大鼠未见变化。多药耐药相关蛋白 2 mRNA 和蛋白在回肠中的表达减少,而 P-糖蛋白 mRNA 在空肠中减少,但蛋白表达未见变化。

讨论和结论

QSYQ 通过抑制回肠中 Mrp2 的表达,增加了口服给予的 ATV 的生物利用度。临床医生应密切关注 ATV 和 QSYQ 之间潜在的药物相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bcc/8745373/b55bf0ab3237/IPHB_A_2021949_F0001_B.jpg

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