A xanthine oxidase inhibitor 1'-acetoxychavicol acetate inhibits azoxymethane-induced colonic aberrant crypt foci in rats

被引:58
作者
Tanaka, T
Makita, H
Kawamori, T
Kawabata, K
Mori, H
Murakami, A
Satoh, K
Hara, A
Ohigashi, H
Koshimizu, K
机构
[1] KINKI UNIV, DEPT BIOTECHNOL SCI, FAC BIOL ORIENTED SCI & TECHNOL, WAKAYAMA 64964, JAPAN
[2] GIFU PHARMACEUT UNIV, DEPT BIOCHEM, GIFU 502, JAPAN
[3] KYOTO UNIV, FAC AGR, DEPT FOOD SCI & TECHNOL, SAKYO KU, KYOTO 60601, JAPAN
关键词
D O I
10.1093/carcin/18.5.1113
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The modifying effect of dietary administration of a xanthine oxidase inhibitor 1'-acetoxychavicol acetate (ACA) present in an edible plant Languas galanga in Thailand on the development of azoxymethane (AOM)-induced colonic aberrant crypt foci (ACF) was investigated in rats. Male F344 rats were given s.c. injections of AOM (15 mg/kg body wt) once a week for 3 weeks to induce colonic ACF. They were fed the diets containing 100 or 200 ppm ACA for 5 weeks, starting 1 week before the first dosing of AOM. At the termination of the study (week 5), AOM induced 118 +/- 28 ACF/colon. Dietary administration of ACA caused significant reduction in the frequency of ACF (41% inhibition by 100 ppm ACA feeding and 37% inhibition by 200 ppm ACA feeding, P<0.01). Such inhibition might be associated with suppression of the proliferation biomarkers' expression such as ornithine decarboxylase activity in the colonic mucosa, number of silver-stained nucleolar organizer regions' protein in the colonic mucosal cell nuclei and blood polyamine content. These results indicate that ACA could inhibit the development of AOM-induced ACF through its suppression of cell proliferation in the colonic mucosa and ACA might be a possible chemopreventive agent against colon tumourigenesis.
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页码:1113 / 1118
页数:6
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