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Comparative Evaluation of Hepatoprotective Activities of Geniposide, Crocins and Crocetin by CCl(4)-Induced liver Injury in Mice
Iridoid glycosides (mainly geniposide) and crocetin derivatives (crocins) are the two major active constituents in Gardenia jasminoides Ellis. In the present study, geniposide, crocins, crocin-1 and crocetin were separated from gardenia chromatographically. Then, mice were orally administrated with...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Applied Pharmacology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774496/ https://www.ncbi.nlm.nih.gov/pubmed/26902084 http://dx.doi.org/10.4062/biomolther.2015.094 |
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author | Chen, Ping Chen, Yang Wang, Yarong Cai, Shining Deng, Liang Liu, Jia Zhang, Hao |
author_facet | Chen, Ping Chen, Yang Wang, Yarong Cai, Shining Deng, Liang Liu, Jia Zhang, Hao |
author_sort | Chen, Ping |
collection | PubMed |
description | Iridoid glycosides (mainly geniposide) and crocetin derivatives (crocins) are the two major active constituents in Gardenia jasminoides Ellis. In the present study, geniposide, crocins, crocin-1 and crocetin were separated from gardenia chromatographically. Then, mice were orally administrated with geniposide (400 mg/kg b.w.), crocins (400 mg/kg b.w.), crocin-1 (400 mg/kg b.w.) and crocetin (140 mg/kg b.w.) once daily for 7 days with CCl(4). Hepatoprotective properties were evaluated by biochemical parameters: Administration of geniposide, crocins, crocin-1and crocetin significantly lowered serum alanine transaminase (ALT), aspartate transaminase (AST) and alkaline phosphatase (ALP) levels in CCl(4)-treated mice. The reduced glutathione (GSH) levels and antioxidant enzymes (SOD and CAT) activities were also increased by geniposide, crocins, crocin-1 and crocetin. Histopathological examination of livers showed that these components reduced deformability, irregular arrangement and rupture of hepatocyte in CCl(4)-treated mice. These biochemical results and liver histopathological assessment demonstrated that geniposide, crocetin derivatives and crocetin show comparative beneficial effects on CCl(4)-induced liver damage via induction of antioxidant defense. Therefore, contents of geniposide and crocetin derivatives should be both considered for hepatoprotective efficacy of Gardenia jasminoides Ellis. |
format | Online Article Text |
id | pubmed-4774496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Society of Applied Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-47744962016-03-28 Comparative Evaluation of Hepatoprotective Activities of Geniposide, Crocins and Crocetin by CCl(4)-Induced liver Injury in Mice Chen, Ping Chen, Yang Wang, Yarong Cai, Shining Deng, Liang Liu, Jia Zhang, Hao Biomol Ther (Seoul) Original Article Iridoid glycosides (mainly geniposide) and crocetin derivatives (crocins) are the two major active constituents in Gardenia jasminoides Ellis. In the present study, geniposide, crocins, crocin-1 and crocetin were separated from gardenia chromatographically. Then, mice were orally administrated with geniposide (400 mg/kg b.w.), crocins (400 mg/kg b.w.), crocin-1 (400 mg/kg b.w.) and crocetin (140 mg/kg b.w.) once daily for 7 days with CCl(4). Hepatoprotective properties were evaluated by biochemical parameters: Administration of geniposide, crocins, crocin-1and crocetin significantly lowered serum alanine transaminase (ALT), aspartate transaminase (AST) and alkaline phosphatase (ALP) levels in CCl(4)-treated mice. The reduced glutathione (GSH) levels and antioxidant enzymes (SOD and CAT) activities were also increased by geniposide, crocins, crocin-1 and crocetin. Histopathological examination of livers showed that these components reduced deformability, irregular arrangement and rupture of hepatocyte in CCl(4)-treated mice. These biochemical results and liver histopathological assessment demonstrated that geniposide, crocetin derivatives and crocetin show comparative beneficial effects on CCl(4)-induced liver damage via induction of antioxidant defense. Therefore, contents of geniposide and crocetin derivatives should be both considered for hepatoprotective efficacy of Gardenia jasminoides Ellis. The Korean Society of Applied Pharmacology 2016-03 2016-03-01 /pmc/articles/PMC4774496/ /pubmed/26902084 http://dx.doi.org/10.4062/biomolther.2015.094 Text en Copyright ©2016, The Korean Society of Applied Pharmacology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Chen, Ping Chen, Yang Wang, Yarong Cai, Shining Deng, Liang Liu, Jia Zhang, Hao Comparative Evaluation of Hepatoprotective Activities of Geniposide, Crocins and Crocetin by CCl(4)-Induced liver Injury in Mice |
title | Comparative Evaluation of Hepatoprotective Activities of Geniposide, Crocins and Crocetin by CCl(4)-Induced liver Injury in Mice |
title_full | Comparative Evaluation of Hepatoprotective Activities of Geniposide, Crocins and Crocetin by CCl(4)-Induced liver Injury in Mice |
title_fullStr | Comparative Evaluation of Hepatoprotective Activities of Geniposide, Crocins and Crocetin by CCl(4)-Induced liver Injury in Mice |
title_full_unstemmed | Comparative Evaluation of Hepatoprotective Activities of Geniposide, Crocins and Crocetin by CCl(4)-Induced liver Injury in Mice |
title_short | Comparative Evaluation of Hepatoprotective Activities of Geniposide, Crocins and Crocetin by CCl(4)-Induced liver Injury in Mice |
title_sort | comparative evaluation of hepatoprotective activities of geniposide, crocins and crocetin by ccl(4)-induced liver injury in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774496/ https://www.ncbi.nlm.nih.gov/pubmed/26902084 http://dx.doi.org/10.4062/biomolther.2015.094 |
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