Difenoconazole disrupts the blood-brain barrier and results in neurotoxicity in carp by inhibiting the Nrf2 pathway mediated ROS accumulation

• Published in: Ecotoxicology and environmental safety Vol. 244; p. 114081
• Main Authors: Liu, Feixue, Wang, Yan, Chen, Li, Bello, Babatunde Kazeem, Zhang, Tianmeng, Yang, Haitao, Li, Xueqing, Pan, Enzhuang, Feng, Huimiao, Dong, Jingquan
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 01-10-2022; Elsevier
• Subjects: Blood-brain barrier; Difenoconazole; Neurotoxicity; Nrf2; ROS; Neurotoxicity; Difenoconazole; Blood-brain barrier; Nrf2; ROS
• ISSN: 0147-6513; 1090-2414
• DOI: 10.1016/j.ecoenv.2022.114081

Excessive use of hard-to-degrade pesticides threatens the ecological health of aquatic systems. This study aimed to investigate difenoconazole (DFZ) residues in the environment induced neurotoxicity in carp and the underlying mechanisms. A total of thirty-six carps were divided into three groups and exposed to 0, 0.5, and 2.0 mg/L DFZ for 96 h, respectively. The alterations in behavior and blood-brain barrier (BBB) were examined, and potential mechanisms were explored using immunological assays and biochemical methods. The results showed that DFZ exposure caused behavioral freezing, reduced feeding, and neuronal necrosis in carp. Mechanistically, DFZ triggered ROS accumulation and destroyed the balance between oxidation and antioxidation with increased lipid peroxidation product MDA contents and reduced antioxidant enzymes SOD and CAT activities in the carp brain by inhibiting the NF-E2-related factor 2 (Nrf2) pathway. The activation of oxidative stress further reduced tight junction proteins and MMP levels, thereby destroying BBB and leading to DFZ leakage into the brain. Increased BBB permeability additionally led to DFZ activation of nuclear factor kappa-B signaling-mediated inflammatory cytokine storm, exacerbating neuroinflammation. Meanwhile, DFZ exposure activated mitochondria-associated apoptosis in the carp’s brain by up-regulating Bcl-2 associated X protein, cleaved-caspase3, and cytochrome C and decreasing B-cell lymphoma-2 levels. Interestingly, the carp’s brain initiated a protective autophagic response via the PI3K/AKT/TOR pathway intending to counteract the neurotoxicity of DFZ. Overall, we concluded that accumulation of DFZ at high concentrations in the aquatic systems disrupted the BBB and resulted in neurotoxicity in carp through inhibition of Nrf2 pathway-mediated ROS accumulation. This study provides a reference for monitoring DFZ residues in the environment and a new target for the treatment of DFZ-induced neurotoxicity in carp.
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•Difenoconazole (DFZ) resulted in altered behavior and brain tissue damage in carp.•Acute DFZ exposure inhibited Nrf2/Keap1 pathway and caused oxidative stress.•DFZ exposure caused ROS accumulation, BBB disruption, and DFZ leakage into the brain.•Disruption of BBB led to DFZ activation of inflammation via the NF-κB pathway.•Disruption of BBB led to DFZ activation of apoptosis via the mitochondrial pathway.