Effects of early florfenicol exposure on glutathione signaling pathway and PPAR signaling pathway in chick liver

转录组 谷胱甘肽 脂质代谢 氧化应激 生物 信号转导 代谢途径 蛋白质组 氟苯尼考 过氧化物酶体增殖物激活受体 药理学 基因 生物化学 基因表达 抗生素
作者
Wei Liu,Xiao Wang,Ying Liu,Siyuan Fang,Zhanjun Wu,Chao Han,Wei Shi,Yongzhan Bao
出处
期刊:Ecotoxicology and Environmental Safety [Elsevier]
卷期号:237: 113529-113529 被引量:7
标识
DOI:10.1016/j.ecoenv.2022.113529
摘要

Florfenicol (FFC) is a common antibiotic for animals. The nonstandard and excessive use of FFC can cause veterinary drug residues in animals, pollute soil and marine environment, and even threaten human health. Therefore, it is necessary to study the toxicity and side effects of FFC on animals. Our previous studies have proved that FFC can cause liver injury in chicks, but there are few in-depth studies on the mechanism of FFC causing liver injury at the level of signaling pathway in chicks. Therefore, transcriptome and proteome sequencing were performed and combined analysis was performed. Sequencing results showed that 1989 genes and 917 proteins were significantly changed in chick livers after FFC exposure. These genes and proteins are related to redox, glutathione transferase activity and lipid metabolism. There are 9 significantly different genes and 7 significantly different proteins in glutathione signaling pathway. Oxidative stress may occur in the liver of chicks through the change of activation state of glutathione signaling pathway. And there are 13 significantly different genes and 18 significantly different proteins in PPAR signaling pathway. The changes of PPAR signaling pathway may induce lipid metabolism disorder in liver. The verification results of qPCR and PRM were consistent with the sequencing results. We also detected GSH-Px, GSH, GST, TG, TC and ANDP levels in liver. These changes of biochemical indicators directly confirmed oxidative stress and lipid metabolism disorders were occurred in the livers of chicks treated by FFC. In conclusion, FFC could induce liver injury in chicks by regulating the expression levels of significantly different genes and proteins in glutathione signaling pathway and PPAR signaling pathway.
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