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Effect of co-administration of Angelicae gigantis radix and Lithospermi radix on rat hepatic injury induced by carbon tetrachloride

BACKGROUND: Co-administration of Angelicae gigantis radix (AGR) and Lithospermi radix (LR) has been commonly applied to patients to treat cardiac and hepatic disorders. Individual bioactivities of these herbal medicines have been widely investigated, but the hepatoprotective effects of co-treatment...

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Autores principales: Lim, Chi-Yeon, Kim, Bu-Yeo, Lim, Se-Hyun, Cho, Su-In
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378140/
https://www.ncbi.nlm.nih.gov/pubmed/25829781
http://dx.doi.org/10.4103/0973-1296.153095
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author Lim, Chi-Yeon
Kim, Bu-Yeo
Lim, Se-Hyun
Cho, Su-In
author_facet Lim, Chi-Yeon
Kim, Bu-Yeo
Lim, Se-Hyun
Cho, Su-In
author_sort Lim, Chi-Yeon
collection PubMed
description BACKGROUND: Co-administration of Angelicae gigantis radix (AGR) and Lithospermi radix (LR) has been commonly applied to patients to treat cardiac and hepatic disorders. Individual bioactivities of these herbal medicines have been widely investigated, but the hepatoprotective effects of co-treatment of AGR and LR have yet to be clarified. OBJECTIVE: The present study investigated the protective effects of extracts of AGR and LR on carbon tetrachloride (CCl(4)) induced hepatic injury. MATERIALS AND METHODS: In this study, we measured the hepatoprotective activity of individual and co-treatment of the two herbal medicines on hepatic injury induced by CCl(4) by measuring different biochemical parameters such as serum aspartate aminotransaminase (AST) and serum alanine aminotransaminase (ALT). Microarray technology also used to compare ontological difference with individual and co-treatment of these two. RESULTS: Combined treatment with AGR and LR (AGR + LR) decreased AST and ALT level in serum which demonstrate hepatoprotective effect of the therapy. When the effect of AGR and LR according to treatment conditions was measured, co-treatment showed the most prominent effect on hepatic injury by CCl(4) rather than individual treatment condition. We further defined gene set that could be the molecular target of herbal effect on hepatic injury by CCl(4) using bioinformatical analysis of interaction network. Highly recovered genes by treating AGR + LR play significant roles in response to hepatic injury induced by CCl(4). CONCLUSION: Combined treatment with AGR and LR showed synergistic protective effects on the CCl(4)-induced rat hepatic tissue injury.
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spelling pubmed-43781402015-04-01 Effect of co-administration of Angelicae gigantis radix and Lithospermi radix on rat hepatic injury induced by carbon tetrachloride Lim, Chi-Yeon Kim, Bu-Yeo Lim, Se-Hyun Cho, Su-In Pharmacogn Mag Original Article BACKGROUND: Co-administration of Angelicae gigantis radix (AGR) and Lithospermi radix (LR) has been commonly applied to patients to treat cardiac and hepatic disorders. Individual bioactivities of these herbal medicines have been widely investigated, but the hepatoprotective effects of co-treatment of AGR and LR have yet to be clarified. OBJECTIVE: The present study investigated the protective effects of extracts of AGR and LR on carbon tetrachloride (CCl(4)) induced hepatic injury. MATERIALS AND METHODS: In this study, we measured the hepatoprotective activity of individual and co-treatment of the two herbal medicines on hepatic injury induced by CCl(4) by measuring different biochemical parameters such as serum aspartate aminotransaminase (AST) and serum alanine aminotransaminase (ALT). Microarray technology also used to compare ontological difference with individual and co-treatment of these two. RESULTS: Combined treatment with AGR and LR (AGR + LR) decreased AST and ALT level in serum which demonstrate hepatoprotective effect of the therapy. When the effect of AGR and LR according to treatment conditions was measured, co-treatment showed the most prominent effect on hepatic injury by CCl(4) rather than individual treatment condition. We further defined gene set that could be the molecular target of herbal effect on hepatic injury by CCl(4) using bioinformatical analysis of interaction network. Highly recovered genes by treating AGR + LR play significant roles in response to hepatic injury induced by CCl(4). CONCLUSION: Combined treatment with AGR and LR showed synergistic protective effects on the CCl(4)-induced rat hepatic tissue injury. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4378140/ /pubmed/25829781 http://dx.doi.org/10.4103/0973-1296.153095 Text en Copyright: © Pharmacognosy Magazine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lim, Chi-Yeon
Kim, Bu-Yeo
Lim, Se-Hyun
Cho, Su-In
Effect of co-administration of Angelicae gigantis radix and Lithospermi radix on rat hepatic injury induced by carbon tetrachloride
title Effect of co-administration of Angelicae gigantis radix and Lithospermi radix on rat hepatic injury induced by carbon tetrachloride
title_full Effect of co-administration of Angelicae gigantis radix and Lithospermi radix on rat hepatic injury induced by carbon tetrachloride
title_fullStr Effect of co-administration of Angelicae gigantis radix and Lithospermi radix on rat hepatic injury induced by carbon tetrachloride
title_full_unstemmed Effect of co-administration of Angelicae gigantis radix and Lithospermi radix on rat hepatic injury induced by carbon tetrachloride
title_short Effect of co-administration of Angelicae gigantis radix and Lithospermi radix on rat hepatic injury induced by carbon tetrachloride
title_sort effect of co-administration of angelicae gigantis radix and lithospermi radix on rat hepatic injury induced by carbon tetrachloride
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4378140/
https://www.ncbi.nlm.nih.gov/pubmed/25829781
http://dx.doi.org/10.4103/0973-1296.153095
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