Literature DB >> 2591011

Antagonistic effect of diethylmaleate on the promotion of forestomach carcinogenesis by butylated hydroxyanisole (BHA) in rats pretreated with N-methyl-N'-nitro-N-nitrosoguanidine.

M Hirose1, M Kagawa, K Ogawa, A Yamamoto, N Ito.   

Abstract

The effects of diethylmaleate (DEM), previously demonstrated to inhibit butylated hydroxyanisole (BHA)-induced forestomach hyperplasia, on BHA promotion of forestomach carcinogenesis in rats pretreated with N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) were examined. Groups of male 6-week-old F344 animals were given a single i.g. administration of 150 mg/kg body weight MNNG and starting 1 week later administered powdered diet containing 1% BHA plus 0.2% DEM, 1% BHA, 0.2% DEM or basal diet alone for 51 weeks. Further groups of rats were treated with 1% BHA plus 0.2% DEM, 1% BHA, 0.2% DEM or basal diet alone without MNNG pretreatment. Histopathological assessment of lesions at week 52 revealed enhancement of MNNG-initiated papilloma (100 versus 50%) and squamous cell carcinoma (100 versus 0%) development by BHA as compared to controls. Additional treatment with DEM, however, significantly reduced the relative incidences of carcinoma in situ (0 versus 35.7%) and squamous cell carcinoma (35.7 versus 100%), as well as BHA-induced forestomach hyperplasia with or without prior MNNG treatment. The results thus clearly demonstrate that DEM acts as a potent antagonist to BHA-promotion of rat forestomach carcinogenesis.

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Year:  1989        PMID: 2591011     DOI: 10.1093/carcin/10.12.2223

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  7 in total

1.  Diethyl maleate, an in vivo chemical depletor of glutathione, affects the response of male and female rats to arsenic deprivation.

Authors:  E O Uthus
Journal:  Biol Trace Elem Res       Date:  1994-12       Impact factor: 3.738

Review 2.  Sixth plot of the carcinogenic potency database: results of animal bioassays published in the General Literature 1989 to 1990 and by the National Toxicology Program 1990 to 1993.

Authors:  L S Gold; N B Manley; T H Slone; G B Garfinkel; B N Ames; L Rohrbach; B R Stern; K Chow
Journal:  Environ Health Perspect       Date:  1995-11       Impact factor: 9.031

3.  Comparison of reversibility of rat forestomach lesions induced by genotoxic and non-genotoxic carcinogens.

Authors:  M Kagawa; K Hakoi; A Yamamoto; M Futakuchi; M Hirose
Journal:  Jpn J Cancer Res       Date:  1993-11

4.  Stomach carcinogenicity of caffeic acid, sesamol and catechol in rats and mice.

Authors:  M Hirose; S Fukushima; T Shirai; R Hasegawa; T Kato; H Tanaka; E Asakawa; N Ito
Journal:  Jpn J Cancer Res       Date:  1990-03

5.  Effects of sodium nitrite and catechol or 3-methoxycatechol in combination on rat stomach epithelium.

Authors:  M Hirose; S Fukushima; R Hasegawa; T Kato; H Tanaka; N Ito
Journal:  Jpn J Cancer Res       Date:  1990-09

6.  Inhibitory effects of antioxidants on N-bis(2-hydroxypropyl)nitrosamine-induced lung carcinogenesis in rats.

Authors:  R Hasegawa; F Furukawa; K Toyoda; M Takahashi; Y Hayashi; M Hirose; N Ito
Journal:  Jpn J Cancer Res       Date:  1990-09

7.  Dose dependence of 1-O-hexyl-2,3,5-trimethylhydroquinone promotion of forestomach carcinogenesis in rats pretreated with N-ethylnitrosourethane.

Authors:  Y Mizoguchi; M Hirose; T Yamaguchi; P Boonyaphiphat; T Miki; T Shirai
Journal:  Jpn J Cancer Res       Date:  1998-05
  7 in total

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