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Hepatotoxic metabolites in Polygoni Multiflori Radix— Comparative toxicology in mice

Polygoni Multiflori Radix (PM) and Rhei radix et rhizoma (rhubarb) contain similar hepatocyte-toxic anthraquinones such as emodin (major free anthraquinone in PM), physcion and their glycosides. In clinical practice, PM hepatotoxicity has been widely reported, although rhubarb is not recognized as h...

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Autores principales: Wang, Shixiao, Kong, Xiang, Chen, Ning, Hu, Pengwei, Boucetta, Hamza, Hu, Zhaoliang, Xu, Xin, Zhang, Pei, Zhan, Xiang, Chang, Ming, Cheng, Rui, Wu, Wei, Song, Min, Lu, Yuting, Hang, Taijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592908/
https://www.ncbi.nlm.nih.gov/pubmed/36304159
http://dx.doi.org/10.3389/fphar.2022.1007284
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author Wang, Shixiao
Kong, Xiang
Chen, Ning
Hu, Pengwei
Boucetta, Hamza
Hu, Zhaoliang
Xu, Xin
Zhang, Pei
Zhan, Xiang
Chang, Ming
Cheng, Rui
Wu, Wei
Song, Min
Lu, Yuting
Hang, Taijun
author_facet Wang, Shixiao
Kong, Xiang
Chen, Ning
Hu, Pengwei
Boucetta, Hamza
Hu, Zhaoliang
Xu, Xin
Zhang, Pei
Zhan, Xiang
Chang, Ming
Cheng, Rui
Wu, Wei
Song, Min
Lu, Yuting
Hang, Taijun
author_sort Wang, Shixiao
collection PubMed
description Polygoni Multiflori Radix (PM) and Rhei radix et rhizoma (rhubarb) contain similar hepatocyte-toxic anthraquinones such as emodin (major free anthraquinone in PM), physcion and their glycosides. In clinical practice, PM hepatotoxicity has been widely reported, although rhubarb is not recognized as hepatotoxic. To clarify the substances basis (key components) of PM hepatotoxicity, based on the characteristic components’ similarity within PM, rhubarb and their concocted forms, a comparative sub-acute toxicity study was designed in mice. Nine groups of mice with 28 days of oral administration of these herbal extracts or 2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside (TSG, major and unique characteristic component in PM)-herb combinations were set as follows: Group-1, control; Group-2, PM ethanol-extract (PME); Group-3, PM praeparata ethanol-extract (PMPE); Group-4, Rhubarb ethanol-extract (RME); Group-5, Steamed rhubarb ethanol-extract (RMPE); Group-6, TSG; Group-7, PMPE-TSG combination; Group-8, RME-TSG combination; Group-9, RMPE-TSG combination. Each experimental group received an equivalent emodin dose of 29 mg/kg except for the TSG group, and an equivalent TSG dose of 1,345 mg/kg except for the PMPE, RME and RMPE groups. The results showed that PME, PMPE-TSG and RME-TSG induced liver lesions and biochemical abnormalities of liver function compared with the control. In contrast, PMPE, RME, RMPE, TSG and RMPE-TSG caused no liver lesions and fewer biochemical abnormalities. Considering the related components, only the co-administration of high doses of TSG and emodin-8-O-β-D-glucoside (EMG, major anthraquinone glycoside in PM) in these groups could cause liver lesions. According to tissue distribution and correlation analysis, EMG dose was positively correlated with the high hepatic emodin and TSG exposure, and the hepatic emodin and TSG exposure were positively correlated with the biochemical abnormalities of liver function. Cell viability test in vitro showed emodin was more hepatotoxic than TSG and EMG, and mainly emodin and TSG of the three had synergistic hepatotoxic effects. Therefore, creatively using rhubarb as a reference, this study revealed that PM hepatotoxicity in mice mainly came from the integrative contribution of TSG, EMG and emodin.
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spelling pubmed-95929082022-10-26 Hepatotoxic metabolites in Polygoni Multiflori Radix— Comparative toxicology in mice Wang, Shixiao Kong, Xiang Chen, Ning Hu, Pengwei Boucetta, Hamza Hu, Zhaoliang Xu, Xin Zhang, Pei Zhan, Xiang Chang, Ming Cheng, Rui Wu, Wei Song, Min Lu, Yuting Hang, Taijun Front Pharmacol Pharmacology Polygoni Multiflori Radix (PM) and Rhei radix et rhizoma (rhubarb) contain similar hepatocyte-toxic anthraquinones such as emodin (major free anthraquinone in PM), physcion and their glycosides. In clinical practice, PM hepatotoxicity has been widely reported, although rhubarb is not recognized as hepatotoxic. To clarify the substances basis (key components) of PM hepatotoxicity, based on the characteristic components’ similarity within PM, rhubarb and their concocted forms, a comparative sub-acute toxicity study was designed in mice. Nine groups of mice with 28 days of oral administration of these herbal extracts or 2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside (TSG, major and unique characteristic component in PM)-herb combinations were set as follows: Group-1, control; Group-2, PM ethanol-extract (PME); Group-3, PM praeparata ethanol-extract (PMPE); Group-4, Rhubarb ethanol-extract (RME); Group-5, Steamed rhubarb ethanol-extract (RMPE); Group-6, TSG; Group-7, PMPE-TSG combination; Group-8, RME-TSG combination; Group-9, RMPE-TSG combination. Each experimental group received an equivalent emodin dose of 29 mg/kg except for the TSG group, and an equivalent TSG dose of 1,345 mg/kg except for the PMPE, RME and RMPE groups. The results showed that PME, PMPE-TSG and RME-TSG induced liver lesions and biochemical abnormalities of liver function compared with the control. In contrast, PMPE, RME, RMPE, TSG and RMPE-TSG caused no liver lesions and fewer biochemical abnormalities. Considering the related components, only the co-administration of high doses of TSG and emodin-8-O-β-D-glucoside (EMG, major anthraquinone glycoside in PM) in these groups could cause liver lesions. According to tissue distribution and correlation analysis, EMG dose was positively correlated with the high hepatic emodin and TSG exposure, and the hepatic emodin and TSG exposure were positively correlated with the biochemical abnormalities of liver function. Cell viability test in vitro showed emodin was more hepatotoxic than TSG and EMG, and mainly emodin and TSG of the three had synergistic hepatotoxic effects. Therefore, creatively using rhubarb as a reference, this study revealed that PM hepatotoxicity in mice mainly came from the integrative contribution of TSG, EMG and emodin. Frontiers Media S.A. 2022-10-11 /pmc/articles/PMC9592908/ /pubmed/36304159 http://dx.doi.org/10.3389/fphar.2022.1007284 Text en Copyright © 2022 Wang, Kong, Chen, Hu, Boucetta, Hu, Xu, Zhang, Zhan, Chang, Cheng, Wu, Song, Lu and Hang. 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 Pharmacology
Wang, Shixiao
Kong, Xiang
Chen, Ning
Hu, Pengwei
Boucetta, Hamza
Hu, Zhaoliang
Xu, Xin
Zhang, Pei
Zhan, Xiang
Chang, Ming
Cheng, Rui
Wu, Wei
Song, Min
Lu, Yuting
Hang, Taijun
Hepatotoxic metabolites in Polygoni Multiflori Radix— Comparative toxicology in mice
title Hepatotoxic metabolites in Polygoni Multiflori Radix— Comparative toxicology in mice
title_full Hepatotoxic metabolites in Polygoni Multiflori Radix— Comparative toxicology in mice
title_fullStr Hepatotoxic metabolites in Polygoni Multiflori Radix— Comparative toxicology in mice
title_full_unstemmed Hepatotoxic metabolites in Polygoni Multiflori Radix— Comparative toxicology in mice
title_short Hepatotoxic metabolites in Polygoni Multiflori Radix— Comparative toxicology in mice
title_sort hepatotoxic metabolites in polygoni multiflori radix— comparative toxicology in mice
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592908/
https://www.ncbi.nlm.nih.gov/pubmed/36304159
http://dx.doi.org/10.3389/fphar.2022.1007284
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