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Chemopreventive effects of silymarin against 1,2-dimethylhydrazine plus dextran sodium sulfate-induced inflammation-associated carcinogenicity and genotoxicity in the colon of gpt delta rats

http://hdl.handle.net/10659/3041
http://hdl.handle.net/10659/3041
4d94a762-ed5b-40ae-b96c-bb278cf2b638
Item type 学術雑誌論文 / Journal Article(1)
公開日 2013-06-04
タイトル
タイトル Chemopreventive effects of silymarin against 1,2-dimethylhydrazine plus dextran sodium sulfate-induced inflammation-associated carcinogenicity and genotoxicity in the colon of gpt delta rats
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Toyoda-Hokaiwado, Naomi

× Toyoda-Hokaiwado, Naomi

WEKO 5008

Toyoda-Hokaiwado, Naomi

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Yasui, Yumiko

× Yasui, Yumiko

WEKO 5009

Yasui, Yumiko

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Muramatsu, Mina

× Muramatsu, Mina

WEKO 5010

Muramatsu, Mina

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Masumura, Kenichi

× Masumura, Kenichi

WEKO 5011

Masumura, Kenichi

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Takamune, Makiko

× Takamune, Makiko

WEKO 5012

Takamune, Makiko

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Yamada, Masami

× Yamada, Masami

WEKO 5013

Yamada, Masami

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Ohta, Toshihiro

× Ohta, Toshihiro

WEKO 5014

Ohta, Toshihiro

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Tanaka, Takuji

× Tanaka, Takuji

WEKO 5015

Tanaka, Takuji

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Nohmi, Takehiko

× Nohmi, Takehiko

WEKO 5016

Nohmi, Takehiko

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抄録
内容記述タイプ Abstract
内容記述 Silymarin, a natural flavonoid from the seeds of milk thistle, is used for chemoprevention against various cancers in clinical settings and in experimental models. To examine the chemopreventive mechanisms of silymarin against colon cancer, we investigated suppressive effects of silymarin against carcinogenicity and genotoxicity induced by 1,2-dimethylhydrazine (DMH) plus dextran sodium sulfate (DSS) in the colon of F344 gpt delta transgenic rats. Male gpt delta rats were given a single subcutaneous injection of 40 mg/kg DMH and followed by 1.5% DSS in drinking water for a week. They were fed diets containing silymarin for 4 weeks, starting 1 week before DMH injection and samples were collected at 4, 20 and 32 weeks after the DMH treatment. Silymarin at doses of 100 and 500 p.p.m. suppressed the tumor formation in a dose-dependent manner and the reduction was statistically significant. In the mutation assays, DMH plus DSS enhanced the gpt mutant frequency (MF) in the colon, and the silymarin treatments reduced the MFs by 20%. Silymarin also reduced the genotoxicity of DMH in a dose-dependent manner in bacterial mutation assay with Salmonella typhimurium YG7108, a sensitive strain to alkylating agents, and the maximum reduction was >80%. These results suggest that silymarin is chemopreventive against DMH/DSS-induced inflammation-associated colon carcinogenesis and silymarin might act as an antigenotoxic agent, in part.
書誌情報 Carcinogenesis

巻 32, 号 10, p. 1512-1517, 発行日 2011-10
ISSN
収録物識別子タイプ ISSN
収録物識別子 0143-3334
DOI
識別子タイプ DOI
関連識別子 10.1093/carcin/bgr130
出版者
出版者 Oxford University Press
資源タイプ
内容記述タイプ Other
内容記述 Article
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