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Chemopreventive Effects of Korean Red Ginseng Extract on Rat Hepatocarcinogenesis
The objective of this study was to determine a chemopreventive activity of Korean red ginseng extract (KRG) in diethylnitrosamine (DEN) induced hepatocarcinogenesis in rats. After acclimatization for a week, Sprague-Dawley rats were randomized into five groups (n = 15) and fed either KRG (0.5, 1 or...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278909/ https://www.ncbi.nlm.nih.gov/pubmed/25553083 http://dx.doi.org/10.7150/jca.10353 |
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author | Kim, Hyemee Hong, Mi-Kyung Choi, Haymie Moon, Hyun-Seuk Lee, Hae-Jeung |
author_facet | Kim, Hyemee Hong, Mi-Kyung Choi, Haymie Moon, Hyun-Seuk Lee, Hae-Jeung |
author_sort | Kim, Hyemee |
collection | PubMed |
description | The objective of this study was to determine a chemopreventive activity of Korean red ginseng extract (KRG) in diethylnitrosamine (DEN) induced hepatocarcinogenesis in rats. After acclimatization for a week, Sprague-Dawley rats were randomized into five groups (n = 15) and fed either KRG (0.5, 1 or 2%) or control diets for 10 weeks. After two weeks of starting of experimental diets, the rats were initiated hepatocarcinogenesis by injection of DEN and were then subjected to two-thirds partial hepatectomy at five-week for developing the medium-term bioassay system. Both 0.5 and 1% KRG diets suppressed the area (55 and 60%; p= 0.0251 and 0.0144) and number (39 and 59%; p= 0.0433 and 0.0012) of glutathione S-transferase placental form (GST-P) positive foci when compared to the DEN-control group. The production of thiobarbituric acid reactive substances (TBARS) was significantly reduced in 0.5 and 1% KRG-treated rats. The supplementation of 1% KRG diet significantly elevated the levels of total glutathione (tGSH) and glutathione-related enzymes including cytosolic glutathione S-transferase (GST) and glutathione peroxidase (GPx) activities. It was also observed in cDNA microarray that the gene expressions (Cyp2c6, Cyp2e1, Cyp3a9, and Mgst1) involved in the xenobiotics metabolism via cytochrome P450 signaling pathway were down-regulated in the 1% KRG diet-treated group when compared to the DEN-control. The chemopreventive effects of KRG could be affected by 1) the decrease of lipid peroxidation, 2) the increase of tGSH content and GSH-dependent enzyme activities, and 3) the decrease of the gene expression profile involved in cytochrome P450 signaling pathway. These results suggest that KRG may prove to be a therapeutic agent against hepatocarcinogenesis. |
format | Online Article Text |
id | pubmed-4278909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-42789092015-01-01 Chemopreventive Effects of Korean Red Ginseng Extract on Rat Hepatocarcinogenesis Kim, Hyemee Hong, Mi-Kyung Choi, Haymie Moon, Hyun-Seuk Lee, Hae-Jeung J Cancer Research Paper The objective of this study was to determine a chemopreventive activity of Korean red ginseng extract (KRG) in diethylnitrosamine (DEN) induced hepatocarcinogenesis in rats. After acclimatization for a week, Sprague-Dawley rats were randomized into five groups (n = 15) and fed either KRG (0.5, 1 or 2%) or control diets for 10 weeks. After two weeks of starting of experimental diets, the rats were initiated hepatocarcinogenesis by injection of DEN and were then subjected to two-thirds partial hepatectomy at five-week for developing the medium-term bioassay system. Both 0.5 and 1% KRG diets suppressed the area (55 and 60%; p= 0.0251 and 0.0144) and number (39 and 59%; p= 0.0433 and 0.0012) of glutathione S-transferase placental form (GST-P) positive foci when compared to the DEN-control group. The production of thiobarbituric acid reactive substances (TBARS) was significantly reduced in 0.5 and 1% KRG-treated rats. The supplementation of 1% KRG diet significantly elevated the levels of total glutathione (tGSH) and glutathione-related enzymes including cytosolic glutathione S-transferase (GST) and glutathione peroxidase (GPx) activities. It was also observed in cDNA microarray that the gene expressions (Cyp2c6, Cyp2e1, Cyp3a9, and Mgst1) involved in the xenobiotics metabolism via cytochrome P450 signaling pathway were down-regulated in the 1% KRG diet-treated group when compared to the DEN-control. The chemopreventive effects of KRG could be affected by 1) the decrease of lipid peroxidation, 2) the increase of tGSH content and GSH-dependent enzyme activities, and 3) the decrease of the gene expression profile involved in cytochrome P450 signaling pathway. These results suggest that KRG may prove to be a therapeutic agent against hepatocarcinogenesis. Ivyspring International Publisher 2015-01-01 /pmc/articles/PMC4278909/ /pubmed/25553083 http://dx.doi.org/10.7150/jca.10353 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. |
spellingShingle | Research Paper Kim, Hyemee Hong, Mi-Kyung Choi, Haymie Moon, Hyun-Seuk Lee, Hae-Jeung Chemopreventive Effects of Korean Red Ginseng Extract on Rat Hepatocarcinogenesis |
title | Chemopreventive Effects of Korean Red Ginseng Extract on Rat Hepatocarcinogenesis |
title_full | Chemopreventive Effects of Korean Red Ginseng Extract on Rat Hepatocarcinogenesis |
title_fullStr | Chemopreventive Effects of Korean Red Ginseng Extract on Rat Hepatocarcinogenesis |
title_full_unstemmed | Chemopreventive Effects of Korean Red Ginseng Extract on Rat Hepatocarcinogenesis |
title_short | Chemopreventive Effects of Korean Red Ginseng Extract on Rat Hepatocarcinogenesis |
title_sort | chemopreventive effects of korean red ginseng extract on rat hepatocarcinogenesis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278909/ https://www.ncbi.nlm.nih.gov/pubmed/25553083 http://dx.doi.org/10.7150/jca.10353 |
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