Literature DB >> 3098717

Sequential changes of the forestomach of F344 rats, Syrian golden hamsters, and B6C3F1 mice treated with butylated hydroxyanisole.

T Masui, M Hirose, K Imaida, S Fukushima, S Tamano, N Ito.   

Abstract

Butylated hydroxyanisole (BHA) was given to F344 rats, Syrian golden hamsters and B6C3F1 mice at 2 doses for up to 104 weeks. The two doses were 2.0% and 1.0% for rats and hamsters, and 1.0% and 0.5% for mice. Animals were sacrificed sequentially at 8-week intervals from week 8 to week 104, and the carcinogenic effects of BHA on the forestomach were examined histopathologically. Papillomas and carcinomas were found in rats, hamsters and mice. In rats, papillomas first appeared in week 8 in the group given the higher level of BHA and in week 56 in that given the lower level. The first carcinoma was observed in week 48 in rats given the high level, while no carcinoma was observed in rats given the lower level. In hamsters, papillomas appeared in week 8 in both BHA-treated groups, and in both groups, the incidence of papillomas was much higher than in BHA-treated rats. Squamous cell carcinomas were observed in 4 hamsters (10.0%) among those that survived more than 64 weeks on treatment with the higher level of BHA and in 4 (7.3%) among those treated with the lower level. In mice, papillomas were induced by BHA in both BHA-treated groups after more than 88 weeks. Although the incidence was not statistically significant, carcinoma was also seen in mice, suggesting that BHA may also be carcinogenic to mouse forestomach.

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Year:  1986        PMID: 3098717

Source DB:  PubMed          Journal:  Jpn J Cancer Res        ISSN: 0910-5050


  7 in total

Review 1.  Recapitulating Human Gastric Cancer Pathogenesis: Experimental Models of Gastric Cancer.

Authors:  Lin Ding; Mohamad El Zaatari; Juanita L Merchant
Journal:  Adv Exp Med Biol       Date:  2016       Impact factor: 2.622

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.  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

5.  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

6.  Reversibility of carcinogen-induced rat forestomach basal cell hyperplasia is due to squamous cell differentiation.

Authors:  K Ogawa; T Hoshiya; T Kato; T Shirai; M Tatematsu
Journal:  Jpn J Cancer Res       Date:  1992-07

7.  The modifying effects of indomethacin or ascorbic acid on cell proliferation induced by different types of bladder tumor promoters in rat urinary bladder and forestomach mucosal epithelium.

Authors:  M A Shibata; S Fukushima; E Asakawa; M Hirose; N Ito
Journal:  Jpn J Cancer Res       Date:  1992-01
  7 in total

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