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Inhibition by ginseng of colon carcinogenesis in rats.

The inhibitory effects of ginseng on the development of 1,2-dimethylhydrazine (DMH)-induced aberrant crypt foci (ACF) in the colon were investigated in rats. Male, 6-week-old rats were injected with DMH once a week for 4 weeks. Rats in Groups 1 and 2 were fed diets containing red and white ginseng,...

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Detalles Bibliográficos
Autores principales: Fukushima, S, Wanibuchi, H, Li, W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3202205/
https://www.ncbi.nlm.nih.gov/pubmed/11748381
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author Fukushima, S
Wanibuchi, H
Li, W
author_facet Fukushima, S
Wanibuchi, H
Li, W
author_sort Fukushima, S
collection PubMed
description The inhibitory effects of ginseng on the development of 1,2-dimethylhydrazine (DMH)-induced aberrant crypt foci (ACF) in the colon were investigated in rats. Male, 6-week-old rats were injected with DMH once a week for 4 weeks. Rats in Groups 1 and 2 were fed diets containing red and white ginseng, respectively, at a dose of 1% for 5 weeks, starting one week before the first treatment of DMH. Animals in Groups 3 and 4 received red or white ginseng for 8 weeks starting after DMH treatment. Group 5 served as a carcinogen control group. Numbers of ACF with at least four crypts were significantly reduced in the colon of Group 2 treated with red ginseng combined with DMH. Moreover, rats were injected with DMH 4 times at one-week intervals. They were also fed diets containing 1% red or white ginseng or the control diet throughout 30 days of the experiment. Treatment with red ginseng resulted in a significant decrease of 5- bromo-2'-deoxyuridine labeling indices in colonic crypts comprising ACF. These findings suggest that dietary administration of red ginseng in combination with DMH suppresses colon carcinogenesis in rats, and the inhibition may be associated, in part, with inhibition of cell proliferation, acting on ACF in the colonic mucosa.
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spelling pubmed-32022052011-10-28 Inhibition by ginseng of colon carcinogenesis in rats. Fukushima, S Wanibuchi, H Li, W J Korean Med Sci Research Article The inhibitory effects of ginseng on the development of 1,2-dimethylhydrazine (DMH)-induced aberrant crypt foci (ACF) in the colon were investigated in rats. Male, 6-week-old rats were injected with DMH once a week for 4 weeks. Rats in Groups 1 and 2 were fed diets containing red and white ginseng, respectively, at a dose of 1% for 5 weeks, starting one week before the first treatment of DMH. Animals in Groups 3 and 4 received red or white ginseng for 8 weeks starting after DMH treatment. Group 5 served as a carcinogen control group. Numbers of ACF with at least four crypts were significantly reduced in the colon of Group 2 treated with red ginseng combined with DMH. Moreover, rats were injected with DMH 4 times at one-week intervals. They were also fed diets containing 1% red or white ginseng or the control diet throughout 30 days of the experiment. Treatment with red ginseng resulted in a significant decrease of 5- bromo-2'-deoxyuridine labeling indices in colonic crypts comprising ACF. These findings suggest that dietary administration of red ginseng in combination with DMH suppresses colon carcinogenesis in rats, and the inhibition may be associated, in part, with inhibition of cell proliferation, acting on ACF in the colonic mucosa. Korean Academy of Medical Sciences 2001-12 /pmc/articles/PMC3202205/ /pubmed/11748381 Text en
spellingShingle Research Article
Fukushima, S
Wanibuchi, H
Li, W
Inhibition by ginseng of colon carcinogenesis in rats.
title Inhibition by ginseng of colon carcinogenesis in rats.
title_full Inhibition by ginseng of colon carcinogenesis in rats.
title_fullStr Inhibition by ginseng of colon carcinogenesis in rats.
title_full_unstemmed Inhibition by ginseng of colon carcinogenesis in rats.
title_short Inhibition by ginseng of colon carcinogenesis in rats.
title_sort inhibition by ginseng of colon carcinogenesis in rats.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3202205/
https://www.ncbi.nlm.nih.gov/pubmed/11748381
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