The influence of dietary fat on hepatic bioactivation of aflatoxin B1 in rats.

J A Hasler, N Dube, C B Nyathi, H Fuhrmann, H P Sallmann
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Abstract

Fischer 344 rats were fed a low-fat high carbohydrate (HC) diet, an isocaloric fat-containing (IC) diet, a hypercaloric fat-containing (HF) diet or a commercial rodent chow. The effects of these diets were studied on the binding of aflatoxin B (AFB1) to exogenous DNA, and on the activities of hepatic glutathione transferases (GSTs), cytochromes 2B1 and 1A1. Microsome-mediated binding of [3H]AFB1 to exogenous DNA was significantly lower in the HC-rats than in the chow and IC-fed rats. No significant differences were noted between HF and either HC or IC rats. There was no significant difference in hepatic GST activity of rats fed the different diets. Our results suggest that high-carbohydrate low-fat diets reduce microsome mediated epoxidation of AFB1 to a larger extent than high-fat diets. In general, high fat diets increased cytochrome 1A1 and 2B1 activities relative to chow and high carbohydrate diet. This suggests greater detoxification of AFB1, thus reducing the amount of AFB1 available for hepatic macromolecular binding.

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饲料脂肪对大鼠肝脏黄曲霉毒素B1生物活性的影响。
Fischer 344大鼠被喂食低脂高碳水化合物(HC)饮食、等热量含脂肪(IC)饮食、高热量含脂肪(HF)饮食或商业啮齿动物饲料。研究了这些饲料对黄曲霉毒素B (AFB1)与外源DNA结合、肝谷胱甘肽转移酶(GSTs)、细胞色素2B1和1A1活性的影响。hc大鼠的微粒体介导的[3H]AFB1与外源DNA的结合明显低于鼠粮和ic喂养大鼠。HF与HC或IC大鼠之间无显著差异。各组大鼠肝脏GST活性无显著差异。我们的研究结果表明,与高脂肪饮食相比,高碳水化合物低脂肪饮食在更大程度上减少了微粒体介导的AFB1环氧化。总体而言,高脂肪饲料相对于食物和高碳水化合物饲料提高了细胞色素1A1和2B1的活性。这表明AFB1的解毒作用更大,从而减少了可用于肝脏大分子结合的AFB1的数量。
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