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The Influence of EGCG on the Pharmacokinetics and Pharmacodynamics of Bisoprolol and a New Method for Simultaneous Determination of EGCG and Bisoprolol in Rat Plasma
BACKGROUND AND AIM: Research has shown that green tea catechins may influence the activity of drug metabolizing enzymes and drug transporters. We examined whether epigallocatechin-3-gallate (EGCG) affected the pharmacokinetics and pharmacodynamics of bisoprolol in rats. METHODS: A sensitive, specifi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9193186/ https://www.ncbi.nlm.nih.gov/pubmed/35711541 http://dx.doi.org/10.3389/fnut.2022.907986 |
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author | Zeng, Weiwei Lao, Sixian Guo, Yi Wu, Yufeng Huang, Min Tomlinson, Brian Zhong, Guoping |
author_facet | Zeng, Weiwei Lao, Sixian Guo, Yi Wu, Yufeng Huang, Min Tomlinson, Brian Zhong, Guoping |
author_sort | Zeng, Weiwei |
collection | PubMed |
description | BACKGROUND AND AIM: Research has shown that green tea catechins may influence the activity of drug metabolizing enzymes and drug transporters. We examined whether epigallocatechin-3-gallate (EGCG) affected the pharmacokinetics and pharmacodynamics of bisoprolol in rats. METHODS: A sensitive, specific liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was established for the quantitative determination of EGCG and bisoprolol. The pharmacokinetic parameters of EGCG and bisoprolol in Sprague-Dawley (SD) rats were analyzed using non-compartmental methods with the aid of the computer program WinNolin. Blood pressure (BP) of spontaneously hypertensive rats (SHRs) was monitored by the tail-cuff method. Bisoprolol was given as single doses of 10 mg/kg with or without EGCG 100 mg/kg by gavage or by intravenous injection. RESULTS: Intake of EGCG with bisoprolol by gavage significantly reduced the C(max) (mean C(max) from 2012.31 to 942.26 ng/mL, P < 0.05) and increased the T(max) (mean T(max) from 0.5 to 0.83 h, P < 0.01) for bisoprolol. After intravenous injection, EGCG significantly increased the apparent volume of distribution of bisoprolol (mean Vz/F from 1629.62 to 2473.27 mL/Kg, P < 0.05) and tended to increase the clearance. The absolute bioavailability of bisoprolol was reduced from 92.04 to 66.05% in rats when bisoprolol was administered with EGCG. Heart rate reduction was less in SHRs when EGCG was given by gavage with bisoprolol whereas BP reduction occurred more rapidly. CONCLUSION: This study showed that the simultaneous administration of EGCG by gavage at a dose of 100 mg/kg was associated with decreased C(max) and increased T(max) of bisoprolol, and the Vz/F of bisoprolol was increased when administered with EGCG by intravenous injection in SD rats. Moreover, the early heart rate reduction with bisoprolol was attenuated and BP reduction occurred earlier when EGCG was given with bisoprolol by gavage in SHRs. |
format | Online Article Text |
id | pubmed-9193186 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91931862022-06-15 The Influence of EGCG on the Pharmacokinetics and Pharmacodynamics of Bisoprolol and a New Method for Simultaneous Determination of EGCG and Bisoprolol in Rat Plasma Zeng, Weiwei Lao, Sixian Guo, Yi Wu, Yufeng Huang, Min Tomlinson, Brian Zhong, Guoping Front Nutr Nutrition BACKGROUND AND AIM: Research has shown that green tea catechins may influence the activity of drug metabolizing enzymes and drug transporters. We examined whether epigallocatechin-3-gallate (EGCG) affected the pharmacokinetics and pharmacodynamics of bisoprolol in rats. METHODS: A sensitive, specific liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was established for the quantitative determination of EGCG and bisoprolol. The pharmacokinetic parameters of EGCG and bisoprolol in Sprague-Dawley (SD) rats were analyzed using non-compartmental methods with the aid of the computer program WinNolin. Blood pressure (BP) of spontaneously hypertensive rats (SHRs) was monitored by the tail-cuff method. Bisoprolol was given as single doses of 10 mg/kg with or without EGCG 100 mg/kg by gavage or by intravenous injection. RESULTS: Intake of EGCG with bisoprolol by gavage significantly reduced the C(max) (mean C(max) from 2012.31 to 942.26 ng/mL, P < 0.05) and increased the T(max) (mean T(max) from 0.5 to 0.83 h, P < 0.01) for bisoprolol. After intravenous injection, EGCG significantly increased the apparent volume of distribution of bisoprolol (mean Vz/F from 1629.62 to 2473.27 mL/Kg, P < 0.05) and tended to increase the clearance. The absolute bioavailability of bisoprolol was reduced from 92.04 to 66.05% in rats when bisoprolol was administered with EGCG. Heart rate reduction was less in SHRs when EGCG was given by gavage with bisoprolol whereas BP reduction occurred more rapidly. CONCLUSION: This study showed that the simultaneous administration of EGCG by gavage at a dose of 100 mg/kg was associated with decreased C(max) and increased T(max) of bisoprolol, and the Vz/F of bisoprolol was increased when administered with EGCG by intravenous injection in SD rats. Moreover, the early heart rate reduction with bisoprolol was attenuated and BP reduction occurred earlier when EGCG was given with bisoprolol by gavage in SHRs. Frontiers Media S.A. 2022-05-31 /pmc/articles/PMC9193186/ /pubmed/35711541 http://dx.doi.org/10.3389/fnut.2022.907986 Text en Copyright © 2022 Zeng, Lao, Guo, Wu, Huang, Tomlinson and Zhong. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Nutrition Zeng, Weiwei Lao, Sixian Guo, Yi Wu, Yufeng Huang, Min Tomlinson, Brian Zhong, Guoping The Influence of EGCG on the Pharmacokinetics and Pharmacodynamics of Bisoprolol and a New Method for Simultaneous Determination of EGCG and Bisoprolol in Rat Plasma |
title | The Influence of EGCG on the Pharmacokinetics and Pharmacodynamics of Bisoprolol and a New Method for Simultaneous Determination of EGCG and Bisoprolol in Rat Plasma |
title_full | The Influence of EGCG on the Pharmacokinetics and Pharmacodynamics of Bisoprolol and a New Method for Simultaneous Determination of EGCG and Bisoprolol in Rat Plasma |
title_fullStr | The Influence of EGCG on the Pharmacokinetics and Pharmacodynamics of Bisoprolol and a New Method for Simultaneous Determination of EGCG and Bisoprolol in Rat Plasma |
title_full_unstemmed | The Influence of EGCG on the Pharmacokinetics and Pharmacodynamics of Bisoprolol and a New Method for Simultaneous Determination of EGCG and Bisoprolol in Rat Plasma |
title_short | The Influence of EGCG on the Pharmacokinetics and Pharmacodynamics of Bisoprolol and a New Method for Simultaneous Determination of EGCG and Bisoprolol in Rat Plasma |
title_sort | influence of egcg on the pharmacokinetics and pharmacodynamics of bisoprolol and a new method for simultaneous determination of egcg and bisoprolol in rat plasma |
topic | Nutrition |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9193186/ https://www.ncbi.nlm.nih.gov/pubmed/35711541 http://dx.doi.org/10.3389/fnut.2022.907986 |
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