首页> 外文期刊>Free radical research >Effect of increased intake of dietary animal fat and fat energy on oxidative damage, mutation frequency, DNA adduct level and DNA repair in rat colon and liver.
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Effect of increased intake of dietary animal fat and fat energy on oxidative damage, mutation frequency, DNA adduct level and DNA repair in rat colon and liver.

机译:饮食动物脂肪和脂肪能量摄入增加对大鼠结肠和肝脏的氧化损伤,突变频率,DNA加合物水平和DNA修复的影响。

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摘要

The effect of high dietary intake of animal fat and an increased fat energy intake on colon and liver genotoxicity and on markers of oxidative damage and antioxidative defence in colon, liver and plasma was investigated in Big Blue rats. The rats were fed ad libitum with semi-synthetic feed supplemented with 0, 3, 10 or 30% w/w lard. After 3 weeks, the mutation frequency, DNA repair gene expression, DNA damage and oxidative markers were determined in liver, colon and plasma. The mutation frequency of the lambda gene cII did not increase with increased fat or energy intake in colon or liver. The DNA-adduct level measured by 32P-postlabelling decreased in both liver and colon with increased fat intake. In liver, this was accompanied by a 2-fold increase of the mRNA level of nucleotide excision repair (NER) gene ERCC1. In colon, a non-statistically significant increase in the ERCC1 mRNA levels was observed. Intake of lard fat resulted in increased ascorbate synthesis and affected markers of oxidative damage to proteins in liver cytosol, but not in plasma. The effect was observed at all lard doses and was not dose-dependent. However, no evidence of increased oxidative DNA damage was found in liver, colon, or urine. Thus, lard intake at the expense of other nutrients and a large increase in the fat energy consumption affects the redox state locally in the liver cytosol, but does not induce DNA-damage, systemic oxidative stress or a dose-dependent increase in mutation frequency in rat colon or liver.
机译:在大蓝大鼠中研究了高膳食饮食动物脂肪摄入和脂肪能量摄入增加对结肠和肝脏遗传毒性以及结肠,肝脏和血浆中氧化损伤和抗氧化防御标志物的影响。随意喂食添加有0、3、10或30%w / w猪油的半合成饲料的大鼠。 3周后,测定肝,结肠和血浆中的突变频率,DNA修复基因表达,DNA损伤和氧化标记。 Lambda基因cII的突变频率不会随着结肠或肝脏中脂肪或能量摄入的增加而增加。通过32P后标记测定的DNA加合物水平在肝脏和结肠中均随着脂肪摄入的增加而降低。在肝脏中,这伴随着核苷酸切除修复(NER)基因ERCC1的mRNA水平增加了2倍。在结肠中,观察到ERCC1 mRNA水平非统计学显着增加。猪油脂肪的摄入会导致抗坏血酸的合成增加,并影响肝细胞溶胶(而非血浆)中蛋白质的氧化损伤标记。在所有猪油剂量下都观察到了这种效果,并且不是剂量依赖性的。但是,在肝脏,结肠或尿液中未发现增加氧化DNA损伤的证据。因此,猪油的摄入以其他营养素为代价,脂肪能量消耗的大量增加会局部影响肝细胞溶胶中的氧化还原状态,但不会引起DNA损伤,系统性氧化应激或突变的剂量依赖性增加。大鼠结肠或肝脏。

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