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Protective Effects of Geniposide and Genipin against Hepatic Ischemia/Reperfusion Injury in Mice

Geniposide is an active product extracted from the gardenia fruit, and is one of the most widely used herbal preparations for liver disorders. This study examined the cytoprotective properties of geniposide and its metabolite, genipin, against hepatic ischemia/reperfusion (I/R) injury. C57BL/6 mice...

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Autores principales: Kim, Joonki, Kim, Hyo-Yeon, Lee, Sun-Mee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Applied Pharmacology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762313/
https://www.ncbi.nlm.nih.gov/pubmed/24009871
http://dx.doi.org/10.4062/biomolther.2013.005
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author Kim, Joonki
Kim, Hyo-Yeon
Lee, Sun-Mee
author_facet Kim, Joonki
Kim, Hyo-Yeon
Lee, Sun-Mee
author_sort Kim, Joonki
collection PubMed
description Geniposide is an active product extracted from the gardenia fruit, and is one of the most widely used herbal preparations for liver disorders. This study examined the cytoprotective properties of geniposide and its metabolite, genipin, against hepatic ischemia/reperfusion (I/R) injury. C57BL/6 mice were subjected to 60 min of ischemia followed by 6 h of reperfusion. Geniposide (100 mg/kg) and genipin (50 mg/kg) were administered orally 30 min before ischemia. In the I/R mice, the levels of serum alanine aminotransferase and hepatic lipid peroxidation were elevated, whereas hepatic glutathione/glutathione disulfide ratio was decreased. These changes were attenuated by geniposide and genipin administration. On the other hand, increased hepatic heme oxygenase-1 protein expression was potentiated by geniposide and genipin administration. The increased levels of tBid, cytochrome c protein expression and caspase-3 activity were attenuated by geniposide and genipin. Increased apoptotic cells in the I/R mice were also significantly reduced by geniposide and genipin treatment. Our results suggest that geniposide and genipin offer significant hepatoprotection against I/R injury by reducing oxidative stress and apoptosis.
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spelling pubmed-37623132013-09-05 Protective Effects of Geniposide and Genipin against Hepatic Ischemia/Reperfusion Injury in Mice Kim, Joonki Kim, Hyo-Yeon Lee, Sun-Mee Biomol Ther (Seoul) Articles Geniposide is an active product extracted from the gardenia fruit, and is one of the most widely used herbal preparations for liver disorders. This study examined the cytoprotective properties of geniposide and its metabolite, genipin, against hepatic ischemia/reperfusion (I/R) injury. C57BL/6 mice were subjected to 60 min of ischemia followed by 6 h of reperfusion. Geniposide (100 mg/kg) and genipin (50 mg/kg) were administered orally 30 min before ischemia. In the I/R mice, the levels of serum alanine aminotransferase and hepatic lipid peroxidation were elevated, whereas hepatic glutathione/glutathione disulfide ratio was decreased. These changes were attenuated by geniposide and genipin administration. On the other hand, increased hepatic heme oxygenase-1 protein expression was potentiated by geniposide and genipin administration. The increased levels of tBid, cytochrome c protein expression and caspase-3 activity were attenuated by geniposide and genipin. Increased apoptotic cells in the I/R mice were also significantly reduced by geniposide and genipin treatment. Our results suggest that geniposide and genipin offer significant hepatoprotection against I/R injury by reducing oxidative stress and apoptosis. The Korean Society of Applied Pharmacology 2013-03 /pmc/articles/PMC3762313/ /pubmed/24009871 http://dx.doi.org/10.4062/biomolther.2013.005 Text en Copyright ©2013, The Korean Society of Applied Pharmacology http://creativecommons.org/licenses/by/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 Articles
Kim, Joonki
Kim, Hyo-Yeon
Lee, Sun-Mee
Protective Effects of Geniposide and Genipin against Hepatic Ischemia/Reperfusion Injury in Mice
title Protective Effects of Geniposide and Genipin against Hepatic Ischemia/Reperfusion Injury in Mice
title_full Protective Effects of Geniposide and Genipin against Hepatic Ischemia/Reperfusion Injury in Mice
title_fullStr Protective Effects of Geniposide and Genipin against Hepatic Ischemia/Reperfusion Injury in Mice
title_full_unstemmed Protective Effects of Geniposide and Genipin against Hepatic Ischemia/Reperfusion Injury in Mice
title_short Protective Effects of Geniposide and Genipin against Hepatic Ischemia/Reperfusion Injury in Mice
title_sort protective effects of geniposide and genipin against hepatic ischemia/reperfusion injury in mice
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762313/
https://www.ncbi.nlm.nih.gov/pubmed/24009871
http://dx.doi.org/10.4062/biomolther.2013.005
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