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Andrographis paniculata Extract and Andrographolide Modulate the Hepatic Drug Metabolism System and Plasma Tolbutamide Concentrations in Rats

Andrographolide is the most abundant terpenoid of A. paniculata which is used in the treatment of diabetes. In this study, we investigated the effects of A. paniculata extract (APE) and andrographolide on the expression of drug-metabolizing enzymes in rat liver and determined whether modulation of t...

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Autores principales: Chen, Haw-Wen, Huang, Chin-Shiu, Liu, Pei-Fen, Li, Chien-Chun, Chen, Chiung-Tong, Liu, Cheng-Tzu, Chiang, Jia-Rong, Yao, Hsien-Tsung, Lii, Chong-Kuei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753754/
https://www.ncbi.nlm.nih.gov/pubmed/23997806
http://dx.doi.org/10.1155/2013/982689
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author Chen, Haw-Wen
Huang, Chin-Shiu
Liu, Pei-Fen
Li, Chien-Chun
Chen, Chiung-Tong
Liu, Cheng-Tzu
Chiang, Jia-Rong
Yao, Hsien-Tsung
Lii, Chong-Kuei
author_facet Chen, Haw-Wen
Huang, Chin-Shiu
Liu, Pei-Fen
Li, Chien-Chun
Chen, Chiung-Tong
Liu, Cheng-Tzu
Chiang, Jia-Rong
Yao, Hsien-Tsung
Lii, Chong-Kuei
author_sort Chen, Haw-Wen
collection PubMed
description Andrographolide is the most abundant terpenoid of A. paniculata which is used in the treatment of diabetes. In this study, we investigated the effects of A. paniculata extract (APE) and andrographolide on the expression of drug-metabolizing enzymes in rat liver and determined whether modulation of these enzymes changed the pharmacokinetics of tolbutamide. Rats were intragastrically dosed with 2 g/kg/day APE or 50 mg/kg/day andrographolide for 5 days before a dose of 20 mg/kg tolbutamide was given. APE and andrographolide reduced the AUC(0–12 h) of tolbutamide by 37% and 18%, respectively, compared with that in controls. The protein and mRNA levels and enzyme activities of CYP2C6/11, CYP1A1/2, and CYP3A1/2 were increased by APE and andrographolide. To evaluate whether APE or andrographolide affected the hypoglycemic action of tolbutamide, high-fat diet-induced obese mice were used and treated in the same manner as the rats. APE and andrographolide increased CYP2C6/11 expression and decreased plasma tolbutamide levels. In a glucose tolerance test, however, the hypoglycemic effect of tolbutamide was not changed by APE or andrographolide. These results suggest that APE and andrographolide accelerate the metabolism rate of tolbutamide through increased expression and activity of drug-metabolizing enzymes. APE and andrographolide, however, do not impair the hypoglycemic effect of tolbutamide.
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spelling pubmed-37537542013-09-01 Andrographis paniculata Extract and Andrographolide Modulate the Hepatic Drug Metabolism System and Plasma Tolbutamide Concentrations in Rats Chen, Haw-Wen Huang, Chin-Shiu Liu, Pei-Fen Li, Chien-Chun Chen, Chiung-Tong Liu, Cheng-Tzu Chiang, Jia-Rong Yao, Hsien-Tsung Lii, Chong-Kuei Evid Based Complement Alternat Med Research Article Andrographolide is the most abundant terpenoid of A. paniculata which is used in the treatment of diabetes. In this study, we investigated the effects of A. paniculata extract (APE) and andrographolide on the expression of drug-metabolizing enzymes in rat liver and determined whether modulation of these enzymes changed the pharmacokinetics of tolbutamide. Rats were intragastrically dosed with 2 g/kg/day APE or 50 mg/kg/day andrographolide for 5 days before a dose of 20 mg/kg tolbutamide was given. APE and andrographolide reduced the AUC(0–12 h) of tolbutamide by 37% and 18%, respectively, compared with that in controls. The protein and mRNA levels and enzyme activities of CYP2C6/11, CYP1A1/2, and CYP3A1/2 were increased by APE and andrographolide. To evaluate whether APE or andrographolide affected the hypoglycemic action of tolbutamide, high-fat diet-induced obese mice were used and treated in the same manner as the rats. APE and andrographolide increased CYP2C6/11 expression and decreased plasma tolbutamide levels. In a glucose tolerance test, however, the hypoglycemic effect of tolbutamide was not changed by APE or andrographolide. These results suggest that APE and andrographolide accelerate the metabolism rate of tolbutamide through increased expression and activity of drug-metabolizing enzymes. APE and andrographolide, however, do not impair the hypoglycemic effect of tolbutamide. Hindawi Publishing Corporation 2013 2013-08-12 /pmc/articles/PMC3753754/ /pubmed/23997806 http://dx.doi.org/10.1155/2013/982689 Text en Copyright © 2013 Haw-Wen Chen et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chen, Haw-Wen
Huang, Chin-Shiu
Liu, Pei-Fen
Li, Chien-Chun
Chen, Chiung-Tong
Liu, Cheng-Tzu
Chiang, Jia-Rong
Yao, Hsien-Tsung
Lii, Chong-Kuei
Andrographis paniculata Extract and Andrographolide Modulate the Hepatic Drug Metabolism System and Plasma Tolbutamide Concentrations in Rats
title Andrographis paniculata Extract and Andrographolide Modulate the Hepatic Drug Metabolism System and Plasma Tolbutamide Concentrations in Rats
title_full Andrographis paniculata Extract and Andrographolide Modulate the Hepatic Drug Metabolism System and Plasma Tolbutamide Concentrations in Rats
title_fullStr Andrographis paniculata Extract and Andrographolide Modulate the Hepatic Drug Metabolism System and Plasma Tolbutamide Concentrations in Rats
title_full_unstemmed Andrographis paniculata Extract and Andrographolide Modulate the Hepatic Drug Metabolism System and Plasma Tolbutamide Concentrations in Rats
title_short Andrographis paniculata Extract and Andrographolide Modulate the Hepatic Drug Metabolism System and Plasma Tolbutamide Concentrations in Rats
title_sort andrographis paniculata extract and andrographolide modulate the hepatic drug metabolism system and plasma tolbutamide concentrations in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753754/
https://www.ncbi.nlm.nih.gov/pubmed/23997806
http://dx.doi.org/10.1155/2013/982689
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