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日粮中摄入 T-2 毒素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。

Toxic effects of dietary exposure to T-2 toxin on intestinal and hepatic biotransformation enzymes and drug transporter systems in broiler chickens.

机构信息

Department of Pharmacology, Toxicology and Biochemistry, Faculty of Veterinary Medicine, Ghent University, Belgium.

出版信息

Food Chem Toxicol. 2013 May;55:150-5. doi: 10.1016/j.fct.2012.12.055. Epub 2013 Jan 11.

Abstract

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 68μg/kg or 752μg/kg T-2 toxin. After 3weeks, 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 752μg/kg T-2. For CYP1A4, even a contamination level of 68μg/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 752μg/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 752μg/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.

摘要

本研究旨在探讨黄曲霉毒素 T-2 对禽类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。肉鸡分别喂食未受污染的饲料、受 68μg/kg 或 752μg/kg T-2 毒素污染的饲料。3 周后,处死动物,采用 qRT-PCR 分析 MDR1、MRP2、CYP1A4、CYP1A5 和 CYP3A37 的 mRNA 表达。在整个小肠中,未观察到明显差异。在肝脏中,暴露于 752μg/kg T-2 的鸡 CYP1A4、CYP1A5 和 CYP3A37 的编码基因表达显著下调。即使接触 68μg/kg T-2 的水平,CYP1A4 的 mRNA 表达也显著降低。肝脏中 MDR1 的表达没有显著降低。相反,暴露于 752μg/kg T-2 后,MRP2 的表达在肝脏中显著下调。为了检测 CYP3A 的酶活性,制备了肝脏和肠道的微粒体。与对照组相比,暴露于 752μg/kg T-2 的鸡回肠和肝脏的 CYP3A 活性显著增加。本研究结果表明,由于长期接触相关剂量的 T-2,药物代谢酶和药物转运机制可能受到影响。

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