Low doses of β‐carotene and lutein inhibit AOM‐induced rat colonic ACF formation but high doses augment ACF incidence

叶黄素 偶氮甲烷 异常隐窝病灶 抗癌原 结直肠癌 医学 致癌物 类胡萝卜素 入射(几何) 内分泌学 内科学 叶黄素 胃肠病学 肿瘤促进 番茄红素 癌症 癌变 生物 生物化学 结肠疾病 物理 光学
作者
Jayadev Raju,Malisetty V. Swamy,Indranie Cooma,Jagan M.R. Patlolla,Brian Pittman,Bandaru S. Reddy,Vernon E. Steele,Chinthalapally V. Rao
出处
期刊:International Journal of Cancer [Wiley]
卷期号:113 (5): 798-802 被引量:38
标识
DOI:10.1002/ijc.20640
摘要

Abstract Epidemiological studies suggest that carotenoids such as β‐carotene and lutein play an important role in reducing the risk for several cancers. However, in colon cancer there is ambiguity with regard to the role of these compounds in that both preventive effects and tumor promotion have been observed. In the present study we observed that male F344 rats were able to tolerate up to 2,500 ppm of β‐carotene as well as of lutein. We have then assessed the chemopreventive efficacy of β‐carotene and lutein at dose levels of ∼4 and 8% of the 2,500 ppm tolerated dose (TD) and also ∼40 and 80% of the TD on azoxymethane (AOM)‐induced colon carcinogenesis, using aberrant crypt foci (ACF) as a surrogate biomarker for colon cancer. Throughout the experiments, 5‐week‐old male F344 rats were fed the control diet (modified AIN‐76A) or experimental diets containing 100 or 200 ppm (∼4 or 8% of the 2,500 ppm TD), or 1,000 or 2,000 ppm (∼40 or 80% of the 2,500 ppm TD) of β‐carotene and lutein ( n =10 rats/group). After 2 weeks on the experimental or control diets, all animals were injected with AOM (15 mg/kg body wt., once weekly for 2 weeks). At 14 weeks of age, all rats were killed, and their colons were evaluated for ACF. Administration of 100 or 200 ppm of β‐carotene inhibited AOM‐induced total colonic ACF formation by 24% ( p <0.01) and 36% ( p <0.001), respectively, whereas lutein at 200 ppm produced a 27% inhibition ( p <0.01) yet had no significant effect at the 100 ppm dose level. Surprisingly, administration of 1,000 or 2,000 ppm of β‐carotene and lutein increased colonic ACF formation in a dose‐dependent manner, i.e ., to 124% and 144% for the former and 110% and 159% for the latter. These results clearly suggest that further studies are warranted to determine whether the increase in ACF incidence by high doses of β‐carotene and lutein will also lead to an increase in tumor outcome. Taken together these data indicate that the chemopreventive activity of β‐carotene and lutein against colon carcinogenesis depends on the dose level. © 2004 Wiley‐Liss, Inc.
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