Abstract

ABSTRACT Introduction Our previous study showed that rice bran oil (RBO) inhibited chemically induced colon carcinogenesis in rats. γ-Oryzanol, a major component in unsaponifiable matter (UM) of RBO, was reported to have an anti-cancer activity in vitro. However, the in vivo effect of γ-oryzanol and UM obtained from RBO on cancer has not been well known. The present study investigated the effect of γ-oryzanol and UM from RBO on colon carcinogenesis in rats. Methods Male F344 rats were fed control diet (C group), diets containing 0.8% γ-oryzanol (O group) or 0.8% UM (U group). 1,2-Dimethylhydrazine (DMH) and dextran sodium sulphate (DSS) were used to induce colon carcinogenesis. After 16 weeks, colons were examined for preneoplastic lesions including aberrant crypt foci (ACF) and mucin-depleted foci (MDF). Catalase and superoxide dismutase (SOD) activities in livers and colons, as well as total antioxidant capacity (TAC) in plasma were measured. Colonic expression of cyclooxygenase-2 (COX-2), a pro-inflammatory protein, was also assessed. Results ACF and MDF were induced by DMH/DSS treatment in all rats of C group. U group had lower MDF incidence and lower numbers of ACF and MDF than did C group; O group had lower number of MDF than did C group. DMH/DSS treatment caused a decrease in colonic catalase and SOD activities, a decrease in TAC and an increase in COX-2 expression, which were improved in U group compared with C group. Colonic SOD activity and COX-2 expression were improved in O group compared with C group. Conclusion γ-Oryzanol and unsaponifiable matter obtained from rice bran oil may suppress chemically induced colon carcinogenesis in rats via mechanisms related to anti-oxidation and anti-inflammation. Unsaponifiable matter from rice bran oil may be more effective than γ-oryzanol.

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