Department of Pharmacology, Toxicology and Biochemistry, Faculty of Veterinary Medicine, Ghent University, Belgium.
Food Chem Toxicol. 2013 May;55:150-5. doi: 10.1016/j.fct.2012.12.055. Epub 2013 Jan 11.
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.
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。