Dietary administration of citrus nobiletin inhibits azoxymethane-induced colonic aberrant crypt foci in rats

被引:75
作者
Kohno, H
Yoshitani, S
Tsukio, Y
Murakami, A
Koshimizu, K
Yano, M
Tokuda, H
Nishino, H
Ohigashi, H
Tanaka, T
机构
[1] Kanazawa Med Univ, Dept Pathol 1, Uchinada, Ishikawa 9200293, Japan
[2] Kanazawa Med Univ, Dept Serol, Uchinada, Ishikawa 9200293, Japan
[3] Kinki Univ, Fac Biol Oriented Sci & Technol, Dept Biotechnol Sci, Wakayama 6496493, Japan
[4] Fruit Tree Res Stn, Dept Citriculture, Shimizu, Shizuoka 4240204, Japan
[5] Kyoto Prefectural Univ Med, Dept Biochem, Kamigyo Ku, Kyoto 6020841, Japan
[6] Kyoto Univ, Grad Sch Agr, Div Appl Life Sci, Kyoto 6060085, Japan
关键词
nobiletin; inhibition; aberrant crypt foci; rat colon;
D O I
10.1016/S0024-3205(01)01169-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
The modifying effects of dietary feeding of a polymethoxyflavonoid nobiletin isolated from Citrus unshiu on the development of azoxymethane (AOM)-induced colonic aberrant crypt foci (ACF) were investigated in male F344 rats. We also assessed the effects of nobiletin on cell proliferation activity of ACF using a monoclonal antibody MIB-5. Rats were given subcutaneous injections of AOM (15 mg/kg body weight) once a week for 3 weeks to induce ACF. They also received the experimental diet containing 0.01% or 0.05% nobiletin for 5 weeks, starting one week before the first dosing of AOM, AOM exposure produced 139 +/- 35 ACF/rat at the end of the study (week 5). Dietary administration of nobiletin caused significant reduction in the frequency of ACF: 70 +/- 15 (50% reduction, p <0.001) at a dose of 0.01% and 63 +/- 10 (55% reduction, p <0.001) at a dose of 0.05%. Nobiletin feeding significantly lowered MIB-5-index in ACF, Also, dietary administration of nobiletin significantly reduced prostaglandin E-2 content in the colonic mucosa. These findings might suggest possible chemopreventive ability of nobiletin, through suppression of cell proliferating activity of ACF, in the development of ACF. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:901 / 913
页数:13
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