Rao C V, Reddy B S
American Health Foundation, Division of Nutritional Carcinogenesis, Valhalla, NY 10595.
Carcinogenesis. 1993 Jul;14(7):1327-33. doi: 10.1093/carcin/14.7.1327.
Epidemiological and laboratory animal model studies suggest that the effect of dietary fat on colon carcinogenesis depends on the amount and its type. In the present study, we investigated the modulating effect of high-fat diets rich in omega-3, omega-6 and omega-9 fatty acids on liver, colon and small intestine mucosal ornithine decarboxylase (ODC) and tyrosine-specific protein kinase (TPK) activities and plasma, liver and colon mucosal prostaglandin E2 (PGE2) and 6-keto prostaglandin F1 alpha (6-keto PGF1 alpha) levels in male F344 rats. At 6 weeks of age, groups of animals were fed the low-fat diet containing 5% corn oil (LFCO), or high-fat diets containing 23.5% corn oil (HFCO), 23.5% olive oil (HFOO) and 20.5% fish oil + 3% corn oil (HFFO). Two weeks later, all animals except the vehicle-treated groups received azoxymethane (AOM) s.c. once weekly for 2 weeks at a dose rate of 15 mg/kg body wt. All animals were killed 5 days later and liver, colon and small intestine mucosa were analyzed for ODC, TPK and PGs and plasma for PGs. Carcinogen treatment enhanced the ODC and TPK activities (P < 0.0001) in the liver and colon of animals, irrespective of dietary treatment. Dietary HFCO compared with LFCO significantly increased the ODC (P < 0.01) and membrane TPK (P < 0.05) activities in the liver and colon of carcinogen-treated animals, whereas the HFOO and HFFO diets significantly (P < 0.002) suppressed the ODC and membrane TPK (P < 0.05) activities in the liver and colon mucosa compared with the HFCO diet. Carcinogen treatment also significantly (P < 0.01) increased the PG levels in plasma, liver and colon. Feeding of the HFFO diet significantly suppressed both the basal levels and ex vivo production of PGE2 and 6-keto PGF1 alpha levels compared with the HFCO diet, whereas the HFOO diet only decreased PGE2 in liver and colon. These results thus demonstrate that high levels of corn oil in the diet increase colon and liver ODC, TPK and PGs whereas high dietary levels of fish oil and olive oil suppress these activities.
流行病学和实验动物模型研究表明,膳食脂肪对结肠癌发生的影响取决于其数量和类型。在本研究中,我们调查了富含ω-3、ω-6和ω-9脂肪酸的高脂饮食对雄性F344大鼠肝脏、结肠和小肠黏膜鸟氨酸脱羧酶(ODC)及酪氨酸特异性蛋白激酶(TPK)活性,以及血浆、肝脏和结肠黏膜前列腺素E2(PGE2)和6-酮前列腺素F1α(6-酮PGF1α)水平的调节作用。6周龄时,将动物分组,分别喂食含5%玉米油的低脂饮食(LFCO),或含23.5%玉米油的高脂饮食(HFCO)、含23.5%橄榄油的高脂饮食(HFOO)和含20.5%鱼油+3%玉米油的高脂饮食(HFFO)。两周后,除溶剂处理组外的所有动物均皮下注射偶氮甲烷(AOM),每周1次,共2周,剂量为15mg/kg体重。5天后处死所有动物,分析肝脏、结肠和小肠黏膜的ODC、TPK和PGs,以及血浆中的PGs。致癌物处理增强了动物肝脏和结肠中的ODC和TPK活性(P<0.0001),与饮食处理无关。与LFCO相比,膳食HFCO显著增加了致癌物处理动物肝脏和结肠中的ODC(P<0.01)和膜TPK(P<0.05)活性,而与HFCO饮食相比,HFOO和HFFO饮食显著(P<0.002)抑制了肝脏和结肠黏膜中的ODC和膜TPK(P<0.05)活性。致癌物处理还显著(P<0.01)增加了血浆、肝脏和结肠中的PG水平。与HFCO饮食相比,喂食HFFO饮食显著抑制了PGE2和6-酮PGF1α水平的基础水平及体外生成,而HFOO饮食仅降低了肝脏和结肠中的PGE2。因此,这些结果表明,饮食中高水平的玉米油会增加结肠和肝脏中的ODC、TPK和PGs,而高膳食水平的鱼油和橄榄油则会抑制这些活性。