Different starting times of alpha-Tocopherol and gamma-tocotrienol supplementation and tumor marker enzyme activities in the rat chemically induced with cancer

被引:15
作者
Makpol, S
Shamaan, NA
Jarien, Z
Top, AGM
Khalid, BAK
Ngah, WZW
机构
[1] UNIV KEBANGSAAN MALAYSIA, FAC MED, DEPT BIOCHEM, KUALA LUMPUR 50300, MALAYSIA
[2] UNIV PERTANIAN MALAYSIA, DEPT BIOCHEM & MICROBIOL, SERDANG 43400, SELANGOR, MALAYSIA
[3] PALM OIL RES INST MALAYSIA, DIV CHEM & TECHNOL, Bangi, SELANGOR, MALAYSIA
[4] UNIV KEBANGSAAN MALAYSIA, DEPT MED, KUALA LUMPUR 50300, MALAYSIA
来源
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM | 1997年 / 28卷 / 04期
关键词
alpha-Tocopherol; gamma-tocotrienal; tumor marker enzymes; rat hepatocarcinogenesis;
D O I
10.1016/S0306-3623(96)00239-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. alpha-Tocopherol ((alpha-T) and gamma-tocotrienol (gamma-T) were supplemented continuously for 8 weeks in the diets of normal rats and rats chemically induced with cancer using diethylnitrosamine (DEN), 2-acetylaminofluorene (AAF) and partial hepatectomy. Hepatocarcinogenesis was followed by determining the plasma gamma-glutamyl-transpeptidase (GGT) and alkaline phosphatase (ALP) activities as well as placental glutathione S-transferase (POST) and GGT activities histochemically, at 4-week intervals. 2. Male Rattus norvegicus were supplemented alpha-T and gamma-T at two different doses of 30 and 300 mg/kg diet. The supplementation was started at three different times: simultaneously with DEN administration; 4 weeks; and 8 weeks after DEN administration. 3. Elevation of plasma GGT activities and formation of PGST and GGT positive foci were attenuated significantly (P < 0.05) when alpha-T and gamma-T were supplemented simultaneously with cancer induction. Supplementation begun 4 and 8 weeks after cancer induction did not affect plasma enzyme activities and formation of enzyme-positive foci. 4. alpha-T was more effective than gamma-T, and a lower dose of 30 mg/kg was found to be more effective in reducing the severity of hepatocarcinogenesis. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:589 / 592
页数:4
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