Influence of Jiegeng on Pharmacokinetic Properties of Flavonoids and Saponins in Gancao

Jiegeng Gancao decoction, which is composed of Jiegeng and Gancao at a weight ratio of 1:2, was widely used for treating pharyngalgia and cough for thousands of years. Our previous work indicated that Gancao could increase the systemic exposure of platycodin D and deapio-platycodin D, two main compo...

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Main Authors: Yancao Mao, Linxiu Peng, An Kang, Tong Xie, Jianya Xu, Cunsi Shen, Jianjian Ji, Liuqing Di, Hao Wu, Jinjun Shan
Format: Article
Language:English
Published: MDPI AG 2017-09-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/22/10/1587
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author Yancao Mao
Linxiu Peng
An Kang
Tong Xie
Jianya Xu
Cunsi Shen
Jianjian Ji
Liuqing Di
Hao Wu
Jinjun Shan
author_facet Yancao Mao
Linxiu Peng
An Kang
Tong Xie
Jianya Xu
Cunsi Shen
Jianjian Ji
Liuqing Di
Hao Wu
Jinjun Shan
author_sort Yancao Mao
collection DOAJ
description Jiegeng Gancao decoction, which is composed of Jiegeng and Gancao at a weight ratio of 1:2, was widely used for treating pharyngalgia and cough for thousands of years. Our previous work indicated that Gancao could increase the systemic exposure of platycodin D and deapio-platycodin D, two main components in Jiegeng. However, whether Jiegeng could alter the pharmacokinetics of the main compounds in Gancao is still unknown. Thus, the purpose of this study was to compare the oral pharmacokinetics of flavonoids and saponins from Gancao alone vs. after co-administration with Jiegeng. Furthermore, Caco-2 cell transport and fecal hydrolysis were investigated to explain the altered pharmacokinetic properties. Pharmacokinetics results suggested that the bioavailability of liquiritin, isoliquiritin, glycyrrhizin and its metabolite, glycyrrhetinic acid, could be improved while bioavailability of liquiritigenin and isoliquiritigenin deteriorated when co-administered with Jiegeng. The Caco-2 transport study showed no significant difference of the Papp values of the main components in Jiegeng Gancao decoction when compared with those in Gancao decoction (p > 0.05). The in vitro metabolism study suggested that saponins and flavonoids glycosides in Gancao were influenced and the metabolic characteristics of most ingredients were consistent with pharmacokinetic results, such as liquiritin and glycyrrhetinic acid. The hydrolysis of liquiritigenin and glycyrrhizin observed with fecal lysate in vitro appeared consistent with the oral pharmacokinetics. Based on experiments, the pharmacokinetic profiles of six components in Gancao were influenced by Jiegeng. The metabolic process might partially contribute to the altered pharmacokinetic behavior. The metabolism of some components of Gancao appeared to be inhibited when coadministered with Jiegeng, possibly by the Jiegeng constituent platycodin.
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spelling doaj.art-4806a5e7bc2d4d698792f15cf66a34ae2022-12-21T19:18:50ZengMDPI AGMolecules1420-30492017-09-012210158710.3390/molecules22101587molecules22101587Influence of Jiegeng on Pharmacokinetic Properties of Flavonoids and Saponins in GancaoYancao Mao0Linxiu Peng1An Kang2Tong Xie3Jianya Xu4Cunsi Shen5Jianjian Ji6Liuqing Di7Hao Wu8Jinjun Shan9Jiangsu Key Laboratory of Pediatric Respiratory Disease, Institute of Pediatrics, Nanjing University of Chinese Medicine, Nanjing 210023, ChinaJiangsu Engineering Research Center for Efficient Delivery System of TCM, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, ChinaJiangsu Engineering Research Center for Efficient Delivery System of TCM, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, ChinaJiangsu Key Laboratory of Pediatric Respiratory Disease, Institute of Pediatrics, Nanjing University of Chinese Medicine, Nanjing 210023, ChinaJiangsu Key Laboratory of Pediatric Respiratory Disease, Institute of Pediatrics, Nanjing University of Chinese Medicine, Nanjing 210023, ChinaJiangsu Key Laboratory of Pediatric Respiratory Disease, Institute of Pediatrics, Nanjing University of Chinese Medicine, Nanjing 210023, ChinaJiangsu Key Laboratory of Pediatric Respiratory Disease, Institute of Pediatrics, Nanjing University of Chinese Medicine, Nanjing 210023, ChinaJiangsu Engineering Research Center for Efficient Delivery System of TCM, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, ChinaJiangsu Engineering Research Center for Efficient Delivery System of TCM, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, ChinaJiangsu Key Laboratory of Pediatric Respiratory Disease, Institute of Pediatrics, Nanjing University of Chinese Medicine, Nanjing 210023, ChinaJiegeng Gancao decoction, which is composed of Jiegeng and Gancao at a weight ratio of 1:2, was widely used for treating pharyngalgia and cough for thousands of years. Our previous work indicated that Gancao could increase the systemic exposure of platycodin D and deapio-platycodin D, two main components in Jiegeng. However, whether Jiegeng could alter the pharmacokinetics of the main compounds in Gancao is still unknown. Thus, the purpose of this study was to compare the oral pharmacokinetics of flavonoids and saponins from Gancao alone vs. after co-administration with Jiegeng. Furthermore, Caco-2 cell transport and fecal hydrolysis were investigated to explain the altered pharmacokinetic properties. Pharmacokinetics results suggested that the bioavailability of liquiritin, isoliquiritin, glycyrrhizin and its metabolite, glycyrrhetinic acid, could be improved while bioavailability of liquiritigenin and isoliquiritigenin deteriorated when co-administered with Jiegeng. The Caco-2 transport study showed no significant difference of the Papp values of the main components in Jiegeng Gancao decoction when compared with those in Gancao decoction (p > 0.05). The in vitro metabolism study suggested that saponins and flavonoids glycosides in Gancao were influenced and the metabolic characteristics of most ingredients were consistent with pharmacokinetic results, such as liquiritin and glycyrrhetinic acid. The hydrolysis of liquiritigenin and glycyrrhizin observed with fecal lysate in vitro appeared consistent with the oral pharmacokinetics. Based on experiments, the pharmacokinetic profiles of six components in Gancao were influenced by Jiegeng. The metabolic process might partially contribute to the altered pharmacokinetic behavior. The metabolism of some components of Gancao appeared to be inhibited when coadministered with Jiegeng, possibly by the Jiegeng constituent platycodin.https://www.mdpi.com/1420-3049/22/10/1587Radix platycodonisGlycyrrhiza uralensis Fischpharmacokineticsabsorptionmetabolism
spellingShingle Yancao Mao
Linxiu Peng
An Kang
Tong Xie
Jianya Xu
Cunsi Shen
Jianjian Ji
Liuqing Di
Hao Wu
Jinjun Shan
Influence of Jiegeng on Pharmacokinetic Properties of Flavonoids and Saponins in Gancao
Molecules
Radix platycodonis
Glycyrrhiza uralensis Fisch
pharmacokinetics
absorption
metabolism
title Influence of Jiegeng on Pharmacokinetic Properties of Flavonoids and Saponins in Gancao
title_full Influence of Jiegeng on Pharmacokinetic Properties of Flavonoids and Saponins in Gancao
title_fullStr Influence of Jiegeng on Pharmacokinetic Properties of Flavonoids and Saponins in Gancao
title_full_unstemmed Influence of Jiegeng on Pharmacokinetic Properties of Flavonoids and Saponins in Gancao
title_short Influence of Jiegeng on Pharmacokinetic Properties of Flavonoids and Saponins in Gancao
title_sort influence of jiegeng on pharmacokinetic properties of flavonoids and saponins in gancao
topic Radix platycodonis
Glycyrrhiza uralensis Fisch
pharmacokinetics
absorption
metabolism
url https://www.mdpi.com/1420-3049/22/10/1587
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