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      Effects of Danshen tablets on pharmacokinetics of atorvastatin calcium in rats and its potential mechanism

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          Abstract

          Context: Danshen tablets (DST), an effective traditional Chinese multi-herbal formula, are often combined with atorvastatin calcium (AC) for treating coronary heart disease in the clinic.

          Objective: This study investigated the effects of DST on the pharmacokinetics of AC and the potential mechanism.

          Materials and methods: The pharmacokinetics of AC (1 mg/kg) with or without pretreatment of DST (100 mg/kg) were investigated using LC-MS/MS. The effects of DST (50 μg/mL) on the metabolic stability of AC were also investigated using rat liver microsome incubation systems.

          Results: The results indicated that C max (23.87 ± 4.27 vs. 38.94 ± 5.32 ng/mL), AUC (0– t ) (41.01 ± 11.32 vs. 77.28 ± 12.92 ng h/mL), and t 1/2 (1.91 ± 0.18 vs. 2.74 ± 0.23 h) decreased significantly ( p < 0.05) when DST and AC were co-administered, which suggested that DST might influence the pharmacokinetic behavior of AC when they are co-administered. The metabolic stability ( t 1/2 ) of AC was also decreased (25.7 ± 5.2 vs. 42.5 ± 6.1) with the pretreatment of DST.

          Discussion and conclusions: This study indicated that the main components in DST could accelerate the metabolism of AC in rat liver microsomes and change the pharmacokinetic behaviors of AC. So these results showed that the herb-drug interaction between DST and AC might occur when they were co-administered. Therefore, the clinical dose of AC should be adjusted when DST and AC are co-administered.

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          Inhibitory effects of sanguinarine on human liver cytochrome P450 enzymes.

          Sanguinarine (SAG) has been recognized as an anticancer drug candidate. However, the drug-drug interactions (DDI) potential for SAG via the inhibition against human cytochrome P450 (CYP) enzymes remains unclear. In the present study, the inhibitory effects of SAG on seven major human CYP isoforms 1A2, 2A6, 2E1, 2D6, 2C8, 2C9 and 3A4 were investigated with human liver microsomes (HLM). The results showed that SAG was a potent noncompetitive inhibitor of CYP2C8 activity (Ki=8.9 μM), and competitive inhibitor of CYP1A2, CYP2C9 and CYP3A4 activities (Ki=2.7, 3.8 and 2.0 μM, respectively). Furthermore, SAG exhibited time- and NADPH-dependent inhibition towards CYP1A2 and CYP3A4 with KI/kinact values of 13.3/0.087 and 5.58/0.029 min(-1) μM(-1), respectively. Weak inhibition of SAG against CYP2E1, CYP2D6 and CYP2A6 was also observed. In vitro-in vivo extrapolation (IV-IVE) from HLM data showed that more than 35.9% of CYP1A2, CYP2C9, CYP2C8 and CYP3A4 activities in vivo could be inhibited by SAG, suggesting that harmful DDIs could occur when SAG or its medical preparations are co-administered with drugs primarily cleared by these CYP isoforms. Further in vivo studies are needed to evaluate the clinical significance of the data presented herein.
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            Cholesterol-independent effects of atorvastatin prevent cardiovascular morbidity and mortality in a mouse model of atherosclerotic plaque rupture

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              Small-Dosing Clinical Study: Pharmacokinetic, Pharmacogenomic ( SLCO2B1 and ABCG2 ), and Interaction (Atorvastatin and Grapefruit Juice) Profiles of 5 Probes for OATP2B1 and BCRP

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                Author and article information

                Journal
                Pharm Biol
                Pharm Biol
                IPHB
                iphb20
                Pharmaceutical Biology
                Taylor & Francis
                1388-0209
                1744-5116
                2018
                11 January 2018
                : 56
                : 1
                : 104-108
                Affiliations
                [a ]Department of Pharmacy, Shanghai Eastern Hepatobiliary Surgery Hospital , Shanghai, China;
                [b ]Department of Pharmacy, Shanghai 9th People's Hospital, Shanghai Jiao Tong University School of Medicine , Shanghai, China;
                [c ]Department of Pharmacy, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine , Shanghai, China
                Author notes
                [*]

                The first two authors contributed equally to this work.

                CONTACT Guoqing Zhang gqzhang@ 123456smmu.edu.cn Department of pharmacy, Shanghai Eastern Hepatobiliary Surgery Hospital , Shanghai200438, China;
                Hai Zhang zhxdks2005@ 123456126.com Department of Pharmacy, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine , 2699 Western Gaoke Rd, Shanghai201204, China
                Article
                1424209
                10.1080/13880209.2018.1424209
                6130457
                29322864
                cfd06753-3f8d-482a-bd1a-daf1b225a725
                © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 18 June 2017
                : 01 November 2017
                : 06 December 2017
                Page count
                Pages: 5, Words: 4016
                Funding
                Funded by: National Natural Science Foundation of China 10.13039/501100001809
                Award ID: 81303192
                Funded by: Scientific Foundation of Shanghai 10.13039/100007219
                Award ID: 15540723500
                This study was financially supported by the Shanghai municipal medical and health discipline construction projects (No. 2017ZZ02015) and the Fundamental Research Funds for the Central Universities (No. 1515219051).
                Categories
                Research Article

                herb-drug interaction,lc-ms/ms,metabolism
                herb-drug interaction, lc-ms/ms, metabolism

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