1Department of Feed Safety, Institute of Physiology and Nutrition, Hungarian University of Agriculture and Life Sciences, Szent István Campus, H-2100 Gödöllő, Hungary.
2HUN-REN-MATE Mycotoxins in the Food Chain Research Group, Hungarian University of Agriculture and Life Sciences, H-7400 Kaposvár, Hungary.
Acta Vet Hung. 2024 Mar 26;72(1):41-50. doi: 10.1556/004.2024.01016. Print 2024 Apr 12.
The study aimed to evaluate the effect of curcumin (CURC) supplementation on broiler chickens exposed to ochratoxin A (OTA), by examining biochemical parameters and the expression of glutathione redox system genes and their regulation. OTA reduced glutathione content in the liver while increasing glutathione peroxidase activity. CURC showed no significant effects. Kidney parameters remained mostly unaffected. Gene expression analysis revealed OTA-induced upregulation of KEAP1, NRF2, AHR, GPx4 and GSR genes in the liver. CURC supplementation led to the upregulation of GPx4 and AHR genes with OTA+CURC treatment, resulting in the downregulation of GPx4, KEAP1, NRF2 and AHR genes compared to OTA treatment alone. In the kidney, GPx4 was downregulated, and NRF2 and AHR were upregulated as an effect of OTA, while CURC upregulated the NRF2 gene only. OTA+CURC treatment led to the downregulation of GPx4, GSS and AHR genes compared to the control and downregulation of NRF2 and AHR genes compared to OTA. The results suggested that CURC is partly effective against OTA-induced oxidative stress and that the effect of OTA and CURC on the antioxidant response is regulated through the KEAP1-NRF2-ARE and AHR pathways.
本研究旨在评估姜黄素 (CURC) 补充剂对暴露于赭曲霉毒素 A (OTA) 的肉鸡的影响,通过检查生化参数以及谷胱甘肽氧化还原系统基因的表达及其调控。OTA 降低了肝脏中的还原型谷胱甘肽含量,同时增加了谷胱甘肽过氧化物酶的活性。CURC 没有显示出显著的效果。肾脏参数基本不受影响。基因表达分析显示,OTA 在肝脏中诱导 KEAP1、NRF2、AHR、GPx4 和 GSR 基因的上调。CURC 补充剂与 OTA 联合处理导致 GPx4 和 AHR 基因的上调,与单独用 OTA 处理相比,导致 GPx4、KEAP1、NRF2 和 AHR 基因的下调。在肾脏中,GPx4 下调,NRF2 和 AHR 上调,这是 OTA 的作用,而 CURC 仅上调 NRF2 基因。与对照组相比,OTA+CURC 处理导致 GPx4、GSS 和 AHR 基因下调,与 OTA 相比,NRF2 和 AHR 基因下调。结果表明,CURC 对 OTA 诱导的氧化应激有一定的作用,OTA 和 CURC 对抗氧化反应的影响是通过 KEAP1-NRF2-ARE 和 AHR 途径进行调控的。