Androgenic activation, impairment of the monoaminergic system and altered behavior in zebrafish larvae exposed to environmental concentrations of fenitrothion
Autor/a
Faria, Melissa
Prats, Eva
Rosas Ramírez, Jonathan Ricardo
Bellot, Marina
Bedrossiantz, Juliette
Pagano, Maria
Valls, Arnau
Gómez Canela, Cristian
Mestres, Jordi
Garcia-Reyero, Natàlia
Faggio, Caterina
Raldúa, Demetrio
Otros/as autores/as
Universitat Ramon Llull. IQS
Fecha de publicación
2021-06-25ISSN
1879-1026
Resumen
Fenitrothion is an organophosphorus insecticide usually found in aquatic ecosystems at concentrations in the range of low ng/L. In this manuscript we show that 24 h exposure to environmental concentrations of fenitrothion, from ng/L to low μg/L, altered basal locomotor activity, visual-motor response and acoustic/vibrational escape response of zebrafish larvae. Furthermore, fenitrothion and expression of gap43a, gfap, atp2b1a, and mbp exhibited a significant non-monotonic concentration-response relationship. Once determined that environmental concentrations of fenitrothion were neurotoxic for zebrafish larvae, a computational analysis identified potential protein targets of this compound. Some of the predictions, including interactions with acetylcholinesterase, monoamine-oxidases and androgen receptor (AR), were experimentally validated. Binding to AR was the most suitable candidate for molecular initiating event, as indicated by both the up-regulation of cyp19a1b and sult2st3 and the non-monotonic relationship found between fenitrothion and the observed responses. Finally, when the integrity of the monoaminergic system was evaluated, altered levels of L-DOPA, DOPAC, HVA and 5-HIAA were found, as well as a significant up-regulation of slc18a2 expression at the lowest concentrations of fenitrothion. These data strongly suggest that concentrations of fenitrothion commonly found in aquatic ecosystems present a significant environmental risk for fish communities.
Tipo de documento
Artículo
Versión del documento
Versión publicada
Lengua
English
Materias (CDU)
615 - Farmacología. Terapéutica. Toxicología. Radiología
Palabras clave
Acetilcolinesterasa
Neurotoxicity
Predicted target profile
Acetylcholinesterase inhibitor
Páginas
13 p.
Publicado por
Elsevier
Publicado en
Science of the Total Environment
Número del acuerdo de la subvención
info:eu-repo/grantAgreement/MICINN i FEDER/PN I+D/CTM2017-83242-R
info:eu-repo/grantAgreement/DEC/SGR/2017 SGR_902
info:eu-repo/grantAgreement/SUR del DEC/Beatriu de Pinós Programme/Grant No. 2016 BP 00233
info:eu-repo/grantAgreement/MICINN i FSE/FI/PRE2018-083513
info:eu-repo/grantAgreement/Sicily region i FSE/FI/Avviso 24/2018
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