SUPPRESSIVE EFFECT OF SESAMIN AGAINST 7,12-DIMETHYLBENZ[A]-ANTHRACENE INDUCED RAT MAMMARY CARCINOGENESIS

被引:0
|
作者
HIROSE, N
DOI, F
UEKI, T
AKAZAWA, K
CHIJIIWA, K
SUGANO, M
AKIMOTO, K
SHIMIZU, S
YAMADA, H
机构
[1] KYOTO UNIV,DEPT AGR CHEM,KYOTO 606,JAPAN
[2] KYUSHU UNIV,SCH AGR 4609,NUTR CHEM LAB,HIGASHI KU,FUKUOKA 812,JAPAN
[3] KYUSHU UNIV HOSP,FAC MED,DEPT SURG 1,FUKUOKA 812,JAPAN
[4] KYUSHU UNIV HOSP,CTR CANC,FUKUOKA 812,JAPAN
[5] KYUSHU UNIV HOSP,FAC MED,DEPT PATHOL 2,FUKUOKA 812,JAPAN
[6] SUNTORY LTD,INST FUNDAMENTAL RES,MICROBIAL SCI LAB,OSAKA 618,JAPAN
关键词
SESAMIN; ALPHA-TOCOPHEROL; DMBA-INDUCED RAT MAMMARY CARCINOMA; PERIPHERAL BLOOD MONONUCLEAR CELLS; PROSTAGLANDIN-E(2);
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The effects of dietary supplementation of sesamin on 7,12-dimethylbenz[a]anthracene (DMBA)-induced mammary carcinogenesis in female Sprague-Dawley rats were studied. Experimental diets containing 0.2% sesamin (an equiweight mixture of sesamin and episesamin) or 0.2% alpha-tocopheryl acetate were given to rats starting 1 week before intragastric administration of DMBA (10 mg/rat). Sesamin significantly (p<0.05) reduced the cumulative number of palpable mammary cancers by 36% at 12 weeks post-DMBA administration compared with animals on a control diet. Alpha-tocopheryl acetate inhibited both the incidence and the cumulative number of mammary tumors by 20% and 45%, respectively. Concentrations of lipid peroxides in plasma, liver and tumors were all decreased in both sesamin and alpha-tocopheryl acetate groups. The activity of peripheral blood mononuclear cells (PBMC) increased in rats fed sesamin (140 to 150% of the control and alpha-tocopheryl acetate groups). Fatty acid compositions of plasma, liver and tumor phosphatidylcholine showed a decreased tendency of the metabolism of linoleic acid to arachidonic acid and hence of the plasma concentration of prostaglandin E2 in the sesamin group. The inhibitory effect of sesamin on DMBA-induced mammary carcinogenesis may be ascribed, at least in part, to immunopotentiation and increased antioxidative activity.
引用
收藏
页码:1259 / 1266
页数:8
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