Integrated network toxicology and molecular docking revealed that 2-ethylhexyldiphenylphosphoric acid induces nephrotoxicity in chickens by activating the ROS/JNK pathway

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Authors: Tian-Chi Tang, Rui-Li Zhang, Xiaoyi Yang, Ling-Huan Luo, Xiangjie Wang, Kunpeng Niu, Ming Ge
Cited by: 2
References: 62

Abstract

2-Ethylhexyl diphenyl phosphate (EHDPHP) is a widely used novel organophosphorus flame retardant. In recent years, EHDPHP has been absorbed into humans and animals through contaminated environments and food intake, causing substantial adverse effects. Therefore, the biological toxicity of EHDPHP has aroused widespread interest among researchers. However, research on the toxic damage mechanism of EHDPHP on the kidneys of poultry is still relatively limited. This study predicted the target sites of EHDPHP through network toxicology and molecular docking. Subsequently, chickens were administered varying concentrations of EHDPHP by oral gavage, and kidney tissues were collected on days 14, 28 and 42 to elucidate its potential nephrotoxic mechanism. Network biology analysis indicates that the predicted targets of EHDPHP and its critical metabolite 5-OH-EHDPHP are significantly enriched in MAPK and apoptotic pathways. The results of molecular docking showed that both EHDPHP and 5-OH-EHDPHP had good binding ability with JNK1/2, suggesting that JNK1/2 was a potential target for EHDPHP. Experimentally, EHDPHP exposure was found to induce oxidative stress, mitochondrial damage and apoptosis in chicken kidneys. These results suggest that kidney injury may be mediated through the activation of the ROS/JNK signaling pathway and the subsequent triggering of apoptosis. In conclusion, our study offers a foundation for further toxicological evaluation and mechanistic investigation of contaminant EHDPHP.

Fields of Study & Subjects

Toxic Organic Pollutants Impact Carcinogens and Genotoxicity Assessment Pesticide Exposure and Toxicity

Publication details

Journal / source
Poultry Science
Publisher
Elsevier BV
Volume
105
Issue
7
Pages
106890–106890
Publication date
1 April 2026
Language
EN