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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...

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Autores principales: Kim, Hyemee, Hong, Mi-Kyung, Choi, Haymie, Moon, Hyun-Seuk, Lee, Hae-Jeung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2015
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.
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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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