1. Academic Validation
  2. Autophagy and PPARs/NF-κB-associated inflammation are involved in hepatotoxicity induced by the synthetic phenolic antioxidant 2,4-di-tert-butylphenol in common carp (Cyprinus carpio)

Autophagy and PPARs/NF-κB-associated inflammation are involved in hepatotoxicity induced by the synthetic phenolic antioxidant 2,4-di-tert-butylphenol in common carp (Cyprinus carpio)

  • Ecotoxicol Environ Saf. 2024 Oct 1:284:116937. doi: 10.1016/j.ecoenv.2024.116937.
Jiaqi Xie 1 Yuxiang Yin 2 Bixiao Lin 3 Xinlian Li 4 Qiuyue Li 4 Xiaoqing Tang 4 Lingai Pan 5 Xuan Xiong 6
Affiliations

Affiliations

  • 1 Hunan Food and Drug Vocational College, Changsha, Hunan Province 410208, China.
  • 2 College of Wildlife and Protected Area, Northeast Forestry University, Harbin, Heilongjiang 150040, China.
  • 3 Department of Health Toxicology, Xiangya School of Public Health, Central South University, Changsha 410013, China.
  • 4 Department of Physiology, College of Basic Medical Sciences, Southwest Medical University, Luzhou, Sichuan Province 646000,, China.
  • 5 Department of Critical Care Medicine, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610072, China. Electronic address: panlingai@med.uestc.edu.cn.
  • 6 Department of Pharmacy, Personalized Drug Therapy Key Laboratory of Sichuan Province, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610072, China. Electronic address: xiongxuan@med.uestc.edu.cn.
Abstract

The synthetic phenolic antioxidant 2,4-di-tert-butylphenol (2,4-DTBP) is an emergent contaminant and can disrupt the delicate balance of aquatic ecosystems. This study aimed to investigate 2,4-DTBP-induced hepatotoxicity in common carp and the underlying mechanisms involved. Sixty common carp were divided into four groups and exposed to 0 mg/L, 0.01 mg/L, 0.1 mg/L or 1 mg/L 2,4-DTBP for 30 days. Here, we first demonstrated that 2,4-DTBP exposure caused liver damage, manifested as hepatocyte nuclear pyknosis, inflammatory cell infiltration and Apoptosis. Moreover, 2,4-DTBP exposure induced hepatic Reactive Oxygen Species (ROS) overload and disrupted antioxidant capacity, as indicated by the reduced activity of the antioxidant Enzymes superoxide dismutase (SOD), catalase (CAT) and Glutathione Peroxidase (GSH-Px). In addition, transmission electron microscopy revealed that 2,4-DTBP exposure induced autophagosome accumulation in the liver of common carp. Western blot analysis further revealed that 2,4-DTBP exposure significantly decreased the protein levels of mTOR and increased the LC3II/LC3I ratio. Furthermore, 2,4-DTBP exposure inhibited lysozyme (LZM) and Alkaline Phosphatase (AKP) activity; decreased immunoglobulin M (IgM), complement 3 (C3), and complement 4 (C4) levels in the serum; increased the mRNA levels of proinflammatory cytokines (NF-κB, TNF-α, IL-1β and IL-6); and increased the mRNA levels of three types of proliferator-activated receptors (PPARs) (α, β/δ and γ). Molecular docking revealed that 2,4-DTBP directly binds to the internal active pocket of PPARs. Overall, we concluded that 2,4-DTBP exposure in aquatic systems could induce hepatotoxicity in common carp by regulating Autophagy and controlling inflammatory responses. The present study provides new insights into the hepatotoxicity mechanism induced by 2,4-DTBP in aquatic organisms and furthers our understanding of the effects of 2,4-DTBP on public health and ecotoxicology.

Keywords

2,4-di-tert-butylphenol (2,4-DTBP); Common carp; Ecotoxicology; Hepatotoxicity; Proliferator-activated receptors (PPARs).

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