Activated FXR promotes xenobiotic metabolism of T-2 toxin and attenuates oxidative stress in broiler chicken liver. (25th January 2020)

• Record Type: Journal Article
• Authors: Dai, Depeng; Pan, Yuanhu; Zeng, CuiPing; Liu, Shenghui; Yan, Yi; Wu, Xiaoxiong; Xu, Zaiyan; Zhang, Lisheng
• Is Part Of: Chemico-biological interactions. Volume 316(2020)
• Publication Date: 2020-01-25
• Subjects: T-2 toxin -- Broiler chicken -- Cholic acid -- Farnesoid X receptor -- Xenobiotic detoxification; Biochemistry -- Periodicals; Toxicological chemistry -- Periodicals; Biochemistry -- Periodicals; Biologie moléculaire -- Périodiques; Biochimie -- Périodiques; Toxicologie biochimique -- Périodiques; 572
• DOI: 10.1016/j.cbi.2019.108912
• Languages: English
• ISSNs: 0009-2797

Abstract

Abstract: The transmission of T-2 toxin and its metabolites into the edible tissues of poultry has potential effects on human health. The bile acid and xenobiotic system composes an intricate physiological network of chemoprotective and transporter-related functions, which ensures the detoxification and removal of harmful xenobiotic and endobiotic compounds from the body. This study revealed that cholic acid (CA), as one of the bile acids, promoted the metabolism of T-2 toxin in vivo by inducing the xenobiotic metabolism enzymes expression, thereby increasing the stress resistance and attenuating the oxidative stress. This study also indicated that dietary supplementation of 1% CA alleviated the mortality caused by T-2 toxin. Liver histology results demonstrated that CA supplementation significantly reduced inflammatory cell infiltration, sinusoidal expansion and congestion. Biochemistry results showed that the elevations of plasma alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities and the increase in concentration of hydrogen peroxide (H2 O2 ) in liver induced by the T-2 toxin were decreased by dietary supplementation of 1% CA. Additionally, CA supplementation led to the increase in superoxide dismutase (SOD) activity, but the decrease in catalase (CAT) activity in broiler chicken livers. Based on these findings, we propose that activation of FXR promotes T-2 toxin xenobiotic metabolism, and FXR plays a hepatoprotection role in liver injury induced by T-2 toxin. Highlights: Bile acid increases the expression of the xenobiotic enzymes. Bile Acid enhances metabolism of T-2 toxin. Bile Acid attenuates oxidative stress.