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Effects of Danshen tablets on pharmacokinetics of amlodipine in rats
Context: Danshen tablets (DST), an effective traditional Chinese multi-herbal formula, are often combined with amlodipine (ALDP) for treating coronary heart disease. Objective: This study investigated the effects of DST on the pharmacokinetics of ALDP and the potential mechanism. Materials and metho...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507817/ https://www.ncbi.nlm.nih.gov/pubmed/31060428 http://dx.doi.org/10.1080/13880209.2019.1604768 |
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author | Zhang, Haixia Han, Xiuyuan Li, Yiqing Li, Hangao Guo, Xichun |
author_facet | Zhang, Haixia Han, Xiuyuan Li, Yiqing Li, Hangao Guo, Xichun |
author_sort | Zhang, Haixia |
collection | PubMed |
description | Context: Danshen tablets (DST), an effective traditional Chinese multi-herbal formula, are often combined with amlodipine (ALDP) for treating coronary heart disease. Objective: This study investigated the effects of DST on the pharmacokinetics of ALDP and the potential mechanism. Materials and methods: The pharmacokinetics of ALDP (1 mg/kg) in male Sprague–Dawley rats (n = 6), with or without pretreatment of DST (100 mg/kg for 7 d), were investigated using LC-MS/MS. The effects of DST on the metabolic stability of ALDP were also investigated using rat liver microsomes (RLM). Results: The results indicated that C(max) (16.25 ± 2.65 vs. 22.79 ± 2.35 ng/ml), AUC((0–)(t)()) (222.87 ± 59.95 vs. 468.32 ± 69.87 n gh/ml), and t(1/2) (10.60 ± 1.05 vs. 14.15 ± 1.59 h) decreased significantly when DST and ALDP were co-administered, which suggested that DST might influence the pharmacokinetic behaviour of ALDP when they are co-administered. The metabolic stability of ALDP was also decreased (23.6 ± 4.7 vs. 38.9 ± 5.2) with the pretreatment of DST. Discussion and conclusions: This study indicated that DST could accelerate the metabolism of ALDP in RLM and change the pharmacokinetic behaviours of ALDP. Accordingly, these results showed that the herb–drug interaction between DST and ALDP might occur when they were co-administered. Therefore, the clinical dose of ALDP should be increased when DST and ALDP are co-administered. |
format | Online Article Text |
id | pubmed-6507817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-65078172019-05-17 Effects of Danshen tablets on pharmacokinetics of amlodipine in rats Zhang, Haixia Han, Xiuyuan Li, Yiqing Li, Hangao Guo, Xichun Pharm Biol Research Article Context: Danshen tablets (DST), an effective traditional Chinese multi-herbal formula, are often combined with amlodipine (ALDP) for treating coronary heart disease. Objective: This study investigated the effects of DST on the pharmacokinetics of ALDP and the potential mechanism. Materials and methods: The pharmacokinetics of ALDP (1 mg/kg) in male Sprague–Dawley rats (n = 6), with or without pretreatment of DST (100 mg/kg for 7 d), were investigated using LC-MS/MS. The effects of DST on the metabolic stability of ALDP were also investigated using rat liver microsomes (RLM). Results: The results indicated that C(max) (16.25 ± 2.65 vs. 22.79 ± 2.35 ng/ml), AUC((0–)(t)()) (222.87 ± 59.95 vs. 468.32 ± 69.87 n gh/ml), and t(1/2) (10.60 ± 1.05 vs. 14.15 ± 1.59 h) decreased significantly when DST and ALDP were co-administered, which suggested that DST might influence the pharmacokinetic behaviour of ALDP when they are co-administered. The metabolic stability of ALDP was also decreased (23.6 ± 4.7 vs. 38.9 ± 5.2) with the pretreatment of DST. Discussion and conclusions: This study indicated that DST could accelerate the metabolism of ALDP in RLM and change the pharmacokinetic behaviours of ALDP. Accordingly, these results showed that the herb–drug interaction between DST and ALDP might occur when they were co-administered. Therefore, the clinical dose of ALDP should be increased when DST and ALDP are co-administered. Taylor & Francis 2019-05-06 /pmc/articles/PMC6507817/ /pubmed/31060428 http://dx.doi.org/10.1080/13880209.2019.1604768 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ 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. |
spellingShingle | Research Article Zhang, Haixia Han, Xiuyuan Li, Yiqing Li, Hangao Guo, Xichun Effects of Danshen tablets on pharmacokinetics of amlodipine in rats |
title | Effects of Danshen tablets on pharmacokinetics of amlodipine in rats |
title_full | Effects of Danshen tablets on pharmacokinetics of amlodipine in rats |
title_fullStr | Effects of Danshen tablets on pharmacokinetics of amlodipine in rats |
title_full_unstemmed | Effects of Danshen tablets on pharmacokinetics of amlodipine in rats |
title_short | Effects of Danshen tablets on pharmacokinetics of amlodipine in rats |
title_sort | effects of danshen tablets on pharmacokinetics of amlodipine in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507817/ https://www.ncbi.nlm.nih.gov/pubmed/31060428 http://dx.doi.org/10.1080/13880209.2019.1604768 |
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