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Primary hippocampal neuronal cell death induction after acute and repeated paraquat exposures mediated by AChE variants alteration and cholinergic and glutamatergic transmission disruption

Authors :
Pino Sans, Javier Del
Moyano-Cires Ivanoff, Paula Viviana
Gómez Díaz, Gloria
Anadón Baselga, María José
Díaz Plaza, María Jesús
García Sánchez, José Manuel
Lobo Alonso, Margarita
Pelayo Alarcón, Adela
Sola Vendrell, Emma
Frejo Moya, María Teresa
Pino Sans, Javier Del
Moyano-Cires Ivanoff, Paula Viviana
Gómez Díaz, Gloria
Anadón Baselga, María José
Díaz Plaza, María Jesús
García Sánchez, José Manuel
Lobo Alonso, Margarita
Pelayo Alarcón, Adela
Sola Vendrell, Emma
Frejo Moya, María Teresa
Publication Year :
2024

Abstract

Paraquat (PQ) is a widely used non-selective contact herbicide shown to produce memory and learning deficits after acute and repeated exposure similar to those induced in Alzheimer's disease (AD). However, the complete mechanisms through which it induces these effects are unknown. On the other hand, cholinergic and glutamatergic systems, mainly in the hippocampus, are involved on learning, memory and cell viability regulation. An alteration of hippocampal cholinergic or glutamatergic transmissions or neuronal cell loss may induce these effects. In this regard, it has been suggested that PQ may induce cell death and affect cholinergic and glutamatergic transmission, which alteration could produce neuronal loss. According to these data, we hypothesized that PQ could induce hippocampal neuronal loss through cholinergic and glutamatergic transmissions alteration. To prove this hypothesis, we evaluated in hippocampal primary cell culture, the PQ toxic effects after 24h and 14 consecutive days exposure on neuronal viability and the cholinergic and glutamatergic mechanisms related to it. This study shows that PQ impaired acetylcholine levels and induced AChE inhibition and increased CHT expression only after 14days exposure, which suggests that acetylcholine levels alteration could be mediated by these actions. PQ also disrupted glutamate levels through induction of glutaminase activity. In addition, PQ induced, after 24h and 14days exposure, cell death on hippocampal neurons that was partially mediated by AChE variants alteration and cholinergic and gultamatergic transmissions disruption. Our present results provide new view of the mechanisms contributing to PQ neurotoxicity and may explain cognitive dysfunctions observed after PQ exposure.<br />Banco Santander<br />Universidad Complutense de Madrid<br />Depto. de Farmacología y Toxicología<br />Fac. de Veterinaria<br />TRUE<br />pub

Details

Database :
OAIster
Notes :
application/pdf, 0300-483X, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1429623589
Document Type :
Electronic Resource