Epoxiconazole profoundly alters rat brain and properties of neural stem cells.


Journal

Chemosphere
ISSN: 1879-1298
Titre abrégé: Chemosphere
Pays: England
ID NLM: 0320657

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 28 05 2021
revised: 09 10 2021
accepted: 19 10 2021
pubmed: 26 10 2021
medline: 18 12 2021
entrez: 25 10 2021
Statut: ppublish

Résumé

Epoxiconazole (EPX), a widely used fungicide for domestic, medical, and industrial applications, could cause neurodegenerative diseases. However, the underling mechanism of neurotoxicity is not well understood. This study aimed to investigate the possible toxic outcomes of Epoxiconzole, a triazole fungicide, on the brain of adult rats in vivo, and in vitro on neural stem cells derived from the subventricular zone of newborn Wistar rats. Our results revealed that oral exposure to EPX at these concentrations (8, 24, 40, 56 mg/kg bw representing respectively NOEL (no observed effect level), NOEL × 3, NOEL × 5, and NOEL × 7) for 28 days caused a considerable generation of oxidative stress in adult rat brain tissue. Furthermore, a significant augmentation in lipid peroxidation and protein oxidation has been found. Moreover, it induced an elevation of DNA fragmentation as assessed by the Comet assay. Indeed, EPX administration impaired activities of antioxidant enzymes and inhibited AChE activity. Concomitantly, this pesticide produced histological alterations in the brain of adult rats. Regarding the embryonic neural stem cells, we demonstrated that the treatment by EPX reduced the viability of cells with an IC50 of 10 μM. It also provoked the reduction of cell proliferation, and EPX triggered arrest in G1/S phase. The neurosphere formation and self-renewal capacity was reduced and associated with decreased differentiation. Moreover, EPX induced cytoskeleton disruption as evidenced by immunocytochemical analysis. Our findings also showed that EPX induced apoptosis as evidenced by a loss of mitochondrial transmembrane potential (ΔΨm) and an activation of caspase-3. In addition, EPX promoted ROS production in neural stem cells. Interestingly, the pretreatment of neural stem cells with the N-acetylcysteine (ROS scavenger) attenuated EPX-induced cell death, disruption of neural stem cells properties, ROS generation and apoptosis. Thus, the use of this hazardous material should be restricted and carefully regulated.

Identifiants

pubmed: 34695486
pii: S0045-6535(21)03112-X
doi: 10.1016/j.chemosphere.2021.132640
pii:
doi:

Substances chimiques

Epoxy Compounds 0
Reactive Oxygen Species 0
Triazoles 0
epoxiconazole U80T84L776

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

132640

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Auteurs

Hiba Hamdi (H)

Laboratory for Research on Biologically Compatible Compounds, Faculty of Dental Medicine, University of Monastir, Avicenne Street, 5019, Monastir, Tunisia; Higher Institute of Biotechnology, University of Monastir, Tunisia.

Imen Graiet (I)

Laboratory for Research on Biologically Compatible Compounds, Faculty of Dental Medicine, University of Monastir, Avicenne Street, 5019, Monastir, Tunisia.

Salwa Abid-Essefi (S)

Laboratory for Research on Biologically Compatible Compounds, Faculty of Dental Medicine, University of Monastir, Avicenne Street, 5019, Monastir, Tunisia.

Joel Eyer (J)

Laboratoire Micro et Nanomédecines Translationnelles (MINT), Inserm 1066, CNRS 6021, Institut de Biologie de La Santé, Centre Hospitalier Universitaire, 49033, Angers, France. Electronic address: joel.eyer@univ-angers.fr.

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Classifications MeSH