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The Neurotoxic Effect of Environmental Temperature Variation in Adult Zebrafish (Danio rerio)

Neurotoxicity consists of the altered functionality of the nervous system caused by exposure to chemical agents or altered chemical–physical parameters. The neurotoxic effect can be evaluated from the molecular to the behavioural level. The zebrafish Danio rerio is a model organism used in many rese...

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Autores principales: Maffioli, Elisa, Nonnis, Simona, Grassi Scalvini, Francesca, Negri, Armando, Tedeschi, Gabriella, Toni, Mattia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10648238/
https://www.ncbi.nlm.nih.gov/pubmed/37958719
http://dx.doi.org/10.3390/ijms242115735
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author Maffioli, Elisa
Nonnis, Simona
Grassi Scalvini, Francesca
Negri, Armando
Tedeschi, Gabriella
Toni, Mattia
author_facet Maffioli, Elisa
Nonnis, Simona
Grassi Scalvini, Francesca
Negri, Armando
Tedeschi, Gabriella
Toni, Mattia
author_sort Maffioli, Elisa
collection PubMed
description Neurotoxicity consists of the altered functionality of the nervous system caused by exposure to chemical agents or altered chemical–physical parameters. The neurotoxic effect can be evaluated from the molecular to the behavioural level. The zebrafish Danio rerio is a model organism used in many research fields, including ecotoxicology and neurotoxicology. Recent studies by our research group have demonstrated that the exposure of adult zebrafish to low (18 °C) or high (34 °C) temperatures alters their brain proteome and fish behaviour compared to control (26 °C). These results showed that thermal variation alters the functionality of the nervous system, suggesting a temperature-induced neurotoxic effect. To demonstrate that temperature variation can be counted among the factors that generate neurotoxicity, eight different protein datasets, previously published by our research group, were subjected to new analyses using an integrated proteomic approach by means of the Ingenuity Pathway Analysis (IPA) software (Release December 2022). The datasets consist of brain proteome analyses of wild type adult zebrafish kept at three different temperatures (18 °C, 26 °C, and 34 °C) for 4 days (acute) or 21 days (chronic treatment), and of BDNF(+/−) and BDNF(−/−) zebrafish kept at 26 °C or 34 °C for 21 days. The results (a) demonstrate that thermal alterations generate an effect that can be defined as neurotoxic (p value ≤ 0.05, activation Z score ≤ −2 or ≥2), (b) identify 16 proteins that can be used as hallmarks of the neurotoxic processes common to all the treatments applied and (c) provide three protein panels (p value ≤ 0.05) related to 18 °C, 34 °C, and BDNF depletion that can be linked to anxiety-like or boldness behaviour upon these treatments.
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spelling pubmed-106482382023-10-29 The Neurotoxic Effect of Environmental Temperature Variation in Adult Zebrafish (Danio rerio) Maffioli, Elisa Nonnis, Simona Grassi Scalvini, Francesca Negri, Armando Tedeschi, Gabriella Toni, Mattia Int J Mol Sci Article Neurotoxicity consists of the altered functionality of the nervous system caused by exposure to chemical agents or altered chemical–physical parameters. The neurotoxic effect can be evaluated from the molecular to the behavioural level. The zebrafish Danio rerio is a model organism used in many research fields, including ecotoxicology and neurotoxicology. Recent studies by our research group have demonstrated that the exposure of adult zebrafish to low (18 °C) or high (34 °C) temperatures alters their brain proteome and fish behaviour compared to control (26 °C). These results showed that thermal variation alters the functionality of the nervous system, suggesting a temperature-induced neurotoxic effect. To demonstrate that temperature variation can be counted among the factors that generate neurotoxicity, eight different protein datasets, previously published by our research group, were subjected to new analyses using an integrated proteomic approach by means of the Ingenuity Pathway Analysis (IPA) software (Release December 2022). The datasets consist of brain proteome analyses of wild type adult zebrafish kept at three different temperatures (18 °C, 26 °C, and 34 °C) for 4 days (acute) or 21 days (chronic treatment), and of BDNF(+/−) and BDNF(−/−) zebrafish kept at 26 °C or 34 °C for 21 days. The results (a) demonstrate that thermal alterations generate an effect that can be defined as neurotoxic (p value ≤ 0.05, activation Z score ≤ −2 or ≥2), (b) identify 16 proteins that can be used as hallmarks of the neurotoxic processes common to all the treatments applied and (c) provide three protein panels (p value ≤ 0.05) related to 18 °C, 34 °C, and BDNF depletion that can be linked to anxiety-like or boldness behaviour upon these treatments. MDPI 2023-10-29 /pmc/articles/PMC10648238/ /pubmed/37958719 http://dx.doi.org/10.3390/ijms242115735 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Maffioli, Elisa
Nonnis, Simona
Grassi Scalvini, Francesca
Negri, Armando
Tedeschi, Gabriella
Toni, Mattia
The Neurotoxic Effect of Environmental Temperature Variation in Adult Zebrafish (Danio rerio)
title The Neurotoxic Effect of Environmental Temperature Variation in Adult Zebrafish (Danio rerio)
title_full The Neurotoxic Effect of Environmental Temperature Variation in Adult Zebrafish (Danio rerio)
title_fullStr The Neurotoxic Effect of Environmental Temperature Variation in Adult Zebrafish (Danio rerio)
title_full_unstemmed The Neurotoxic Effect of Environmental Temperature Variation in Adult Zebrafish (Danio rerio)
title_short The Neurotoxic Effect of Environmental Temperature Variation in Adult Zebrafish (Danio rerio)
title_sort neurotoxic effect of environmental temperature variation in adult zebrafish (danio rerio)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10648238/
https://www.ncbi.nlm.nih.gov/pubmed/37958719
http://dx.doi.org/10.3390/ijms242115735
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