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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Toxic effects of dietary exposure to T-2 toxin on intestinal and hepatic biotransformation enzymes and drug transporter systems in broiler chickens
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Toxic effects of dietary exposure to T-2 toxin on intestinal and hepatic biotransformation enzymes and drug transporter systems in broiler chickens

机译:饮食中T-2毒素暴露对肉鸡肠道和肝脏生物转化酶及药物转运系统的毒性作用

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摘要

The effects of the mycotoxin T-2 on hepatic and intestinal drug-metabolizing enzymes (cytochrome P450) and drug transporter systems (MDR1 and MRP2) in poultry were investigated during this study. Broiler chickens received either uncontaminated feed, feed contaminated with 68 μg/kg or 752 μg/kg T-2 toxin. After 3. weeks, the animals were euthanized and MDR1, MRP2, CYP1A4, CYP1A5 and CYP3A37 mRNA expression were analyzed using qRT-PCR. Along the entire length of the small intestine no significant differences were observed. In the liver, genes coding for CYP1A4, CYP1A5 and CYP3A37 were significantly down-regulated in the group exposed to 752 μg/kg T-2. For CYP1A4, even a contamination level of 68 μg/kg T-2 caused a significant decrease in mRNA expression. Expression of MDR1 was not significantly decreased in the liver. In contrast, hepatic MRP2 expression was significantly down-regulated after exposure to 752 μg/kg T-2. Hepatic and intestinal microsomes were prepared to test the enzymatic activity of CYP3A. In the ileum and liver CYP3A activity was significantly increased in the group receiving 752 μg/kg T-2 compared to the control group. The results of this study show that drug metabolizing enzymes and drug transporter mechanisms can be influenced due to prolonged exposure to relevant doses of T-2.
机译:在本研究中,研究了真菌毒素T-2对家禽肝脏和肠道药物代谢酶(细胞色素P450)和药物转运系统(MDR1和MRP2)的影响。肉鸡只接受未污染的饲料,被68μg/ kg或752μg/ kg T-2毒素污染的饲料。 3周后,对动物实施安乐死并使用qRT-PCR分析MDR1,MRP2,CYP1A4,CYP1A5和CYP3A37 mRNA的表达。沿小肠的整个长度未观察到显着差异。在肝脏中,暴露于752μg/ kg T-2的组中编码CYP1A4,CYP1A5和CYP3A37的基因显着下调。对于CYP1A4,即使是68μg/ kg T-2的污染水平也会导致mRNA表达显着下降。肝脏中MDR1的表达没有明显降低。相反,暴露于752μg/ kg T-2后,肝MRP2表达显着下调。制备肝和肠微粒体以测试CYP3A的酶活性。在回肠和肝脏中,与对照组相比,接受752μg/ kg T-2的组中CYP3A活性显着增加。这项研究的结果表明,由于长期暴露于相关剂量的T-2中,药物代谢酶和药物转运机制可能会受到影响。

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