Fungicide Residues Exposure and [Formula: see text] Aggregation in a Mouse Model of Alzheimer’s Disease

BACKGROUND: Pesticide residues have contaminated our environment and nutrition over the last century. Although these compounds are present at very low concentrations, their long-term effects on human health is of concern. The link between pesticide residues and Alzheimer’s disease is not clear and difficult to establish. To date, no in vivo experiments have yet modeled the impact of this chronic contamination on neurodegenerative disorders. OBJECTIVES: We investigated the impact of fungicide residues on the pathological markers of Alzheimer’s disease in a transgenic mouse model. METHODS: Transgenic (J20, [Formula: see text]) mice were chronically exposed to a cocktail of residues of cyprodinil, mepanipyrim, and pyrimethanil at [Formula: see text] in their drinking water for 9 months. We assessed the effects of fungicide residues on the pathological markers of the disease including [Formula: see text] aggregates, neuroinflammation, and neuronal loss. Then, we studied the dynamics of [Formula: see text] aggregation in vivo via a longitudinal study using two-photon microscopy. Finally, we investigated the molecular mechanisms involved in the production and clearance of [Formula: see text] peptides. RESULTS: We found that a chronic exposure to three fungicide residues exacerbated aggregation, microgliosis, and neuronal loss. These fungicides also increased vascular amyloid aggregates reminiscent of cerebral amyloid angiopathy between 6 and 9 months of treatment. The mechanism of action revealed that fungicides promoted [Formula: see text] peptide fibril formation in vitro and involved an in vivo overexpression of the levels of the [Formula: see text] –cleaving enzyme (BACE1) combined with impairment of [Formula: see text] clearance through neprylisin (NEP). CONCLUSIONS: Chronic exposure of the J20 mouse model of Alzheimer’s disease to a cocktail of fungicides, at the regulatory concentration allowed in tap water ([Formula: see text]), strengthened the preexisting pathological markers: neuroinflammation, [Formula: see text] aggregation, and APP [Formula: see text]. We hypothesize prevention strategies toward pesticide long-term exposure may be an alternative to counterbalance the lack of treatment and to slow down the worldwide Alzheimer’s epidemic. https://doi.org/10.1289/EHP5550