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Polystyrene nanoplastics disrupt glucose metabolism and cortisol levels with a possible link to behavioural changes in larval zebrafish

Plastic nanoparticles originating from weathering plastic waste are emerging contaminants in aquatic environments, with unknown modes of action in aquatic organisms. Recent studies suggest that internalised nanoplastics may disrupt processes related to energy metabolism. Such disruption can be cruci...

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Autores principales: Brun, Nadja R., van Hage, Patrick, Hunting, Ellard R., Haramis, Anna-Pavlina G., Vink, Suzanne C., Vijver, Martina G., Schaaf, Marcel J. M., Tudorache, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802380/
https://www.ncbi.nlm.nih.gov/pubmed/31646185
http://dx.doi.org/10.1038/s42003-019-0629-6
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author Brun, Nadja R.
van Hage, Patrick
Hunting, Ellard R.
Haramis, Anna-Pavlina G.
Vink, Suzanne C.
Vijver, Martina G.
Schaaf, Marcel J. M.
Tudorache, Christian
author_facet Brun, Nadja R.
van Hage, Patrick
Hunting, Ellard R.
Haramis, Anna-Pavlina G.
Vink, Suzanne C.
Vijver, Martina G.
Schaaf, Marcel J. M.
Tudorache, Christian
author_sort Brun, Nadja R.
collection PubMed
description Plastic nanoparticles originating from weathering plastic waste are emerging contaminants in aquatic environments, with unknown modes of action in aquatic organisms. Recent studies suggest that internalised nanoplastics may disrupt processes related to energy metabolism. Such disruption can be crucial for organisms during development and may ultimately lead to changes in behaviour. Here, we investigated the link between polystyrene nanoplastic (PSNP)-induced signalling events and behavioural changes. Larval zebrafish exhibited PSNP accumulation in the pancreas, which coincided with a decreased glucose level. By using hyperglycemic and glucocorticoid receptor (Gr) mutant larvae, we demonstrate that the PSNP-induced disruption in glucose homoeostasis coincided with increased cortisol secretion and hyperactivity in challenge phases. Our work sheds new light on a potential mechanism underlying nanoplastics toxicity in fish, suggesting that the adverse effect of PSNPs are at least in part mediated by Gr activation in response to disrupted glucose homeostasis, ultimately leading to aberrant locomotor activity.
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spelling pubmed-68023802019-10-23 Polystyrene nanoplastics disrupt glucose metabolism and cortisol levels with a possible link to behavioural changes in larval zebrafish Brun, Nadja R. van Hage, Patrick Hunting, Ellard R. Haramis, Anna-Pavlina G. Vink, Suzanne C. Vijver, Martina G. Schaaf, Marcel J. M. Tudorache, Christian Commun Biol Article Plastic nanoparticles originating from weathering plastic waste are emerging contaminants in aquatic environments, with unknown modes of action in aquatic organisms. Recent studies suggest that internalised nanoplastics may disrupt processes related to energy metabolism. Such disruption can be crucial for organisms during development and may ultimately lead to changes in behaviour. Here, we investigated the link between polystyrene nanoplastic (PSNP)-induced signalling events and behavioural changes. Larval zebrafish exhibited PSNP accumulation in the pancreas, which coincided with a decreased glucose level. By using hyperglycemic and glucocorticoid receptor (Gr) mutant larvae, we demonstrate that the PSNP-induced disruption in glucose homoeostasis coincided with increased cortisol secretion and hyperactivity in challenge phases. Our work sheds new light on a potential mechanism underlying nanoplastics toxicity in fish, suggesting that the adverse effect of PSNPs are at least in part mediated by Gr activation in response to disrupted glucose homeostasis, ultimately leading to aberrant locomotor activity. Nature Publishing Group UK 2019-10-18 /pmc/articles/PMC6802380/ /pubmed/31646185 http://dx.doi.org/10.1038/s42003-019-0629-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Brun, Nadja R.
van Hage, Patrick
Hunting, Ellard R.
Haramis, Anna-Pavlina G.
Vink, Suzanne C.
Vijver, Martina G.
Schaaf, Marcel J. M.
Tudorache, Christian
Polystyrene nanoplastics disrupt glucose metabolism and cortisol levels with a possible link to behavioural changes in larval zebrafish
title Polystyrene nanoplastics disrupt glucose metabolism and cortisol levels with a possible link to behavioural changes in larval zebrafish
title_full Polystyrene nanoplastics disrupt glucose metabolism and cortisol levels with a possible link to behavioural changes in larval zebrafish
title_fullStr Polystyrene nanoplastics disrupt glucose metabolism and cortisol levels with a possible link to behavioural changes in larval zebrafish
title_full_unstemmed Polystyrene nanoplastics disrupt glucose metabolism and cortisol levels with a possible link to behavioural changes in larval zebrafish
title_short Polystyrene nanoplastics disrupt glucose metabolism and cortisol levels with a possible link to behavioural changes in larval zebrafish
title_sort polystyrene nanoplastics disrupt glucose metabolism and cortisol levels with a possible link to behavioural changes in larval zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6802380/
https://www.ncbi.nlm.nih.gov/pubmed/31646185
http://dx.doi.org/10.1038/s42003-019-0629-6
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