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Glutathione and its dependent enzymes’ modulatory responses to neonicotinoid insecticide sulfoxaflor induced oxidative damage in zebrafish in vivo

The use of neonicotinoid insecticides has progressively increased worldwide when compared with other insecticide groups. Due to this increase, non-target animal species such as fish are exposed to neonicotinoids from different sources, so they can be accumulated at trophic levels and cause various t...

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Autores principales: Piner Benli, Petek, Çelik, Mehmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454941/
https://www.ncbi.nlm.nih.gov/pubmed/34176341
http://dx.doi.org/10.1177/00368504211028361
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author Piner Benli, Petek
Çelik, Mehmet
author_facet Piner Benli, Petek
Çelik, Mehmet
author_sort Piner Benli, Petek
collection PubMed
description The use of neonicotinoid insecticides has progressively increased worldwide when compared with other insecticide groups. Due to this increase, non-target animal species such as fish are exposed to neonicotinoids from different sources, so they can be accumulated at trophic levels and cause various toxic effects by reaching humans. There are limited studies related to the toxic effects of neonicotinoid sulfoximine insecticides including sulfoxaflor on non-target species. The purpose of the present study was to evaluate the effects of sulfoxaflor on GSH-related antioxidants and to determine oxidative stress-producing effect of sulfoxaflor in the gill of zebrafish (Danio rerio). For this purpose, three sublethal concentrations of sulfoxaflor 0.87 mg/L (2.5% of 96 h LC(50)), 1.75 mg/L (5% of 96 h LC(50)), 3.51 mg/L (10% of 96 h LC(50)) of sulfoxaflor were exposed to zebrafish for 24, 48, and 96 h. GSH related antioxidants were evaluated by analyzing tGSH levels and GPx, GR, GST specific enzyme activities in the gill of zebrafish. The oxidative damage of sulfoxaflor on gill cells was determined by measuring TBARS levels. The results of this study demonstrated that sulfoxaflor activated GSH related antioxidants by increasing tGSH levels, GPx, GR enzyme activities and by diminishing GST enzyme activity in the gill of zebrafish. Sulfoxaflor also caused oxidative damage in the gill of zebrafish by increasing lipid peroxidation. In conclusion, this study indicated that sulfoxaflor led to oxidative stress and activation of GSH related antioxidants in the gill of zebrafish.
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spelling pubmed-104549412023-08-26 Glutathione and its dependent enzymes’ modulatory responses to neonicotinoid insecticide sulfoxaflor induced oxidative damage in zebrafish in vivo Piner Benli, Petek Çelik, Mehmet Sci Prog Article The use of neonicotinoid insecticides has progressively increased worldwide when compared with other insecticide groups. Due to this increase, non-target animal species such as fish are exposed to neonicotinoids from different sources, so they can be accumulated at trophic levels and cause various toxic effects by reaching humans. There are limited studies related to the toxic effects of neonicotinoid sulfoximine insecticides including sulfoxaflor on non-target species. The purpose of the present study was to evaluate the effects of sulfoxaflor on GSH-related antioxidants and to determine oxidative stress-producing effect of sulfoxaflor in the gill of zebrafish (Danio rerio). For this purpose, three sublethal concentrations of sulfoxaflor 0.87 mg/L (2.5% of 96 h LC(50)), 1.75 mg/L (5% of 96 h LC(50)), 3.51 mg/L (10% of 96 h LC(50)) of sulfoxaflor were exposed to zebrafish for 24, 48, and 96 h. GSH related antioxidants were evaluated by analyzing tGSH levels and GPx, GR, GST specific enzyme activities in the gill of zebrafish. The oxidative damage of sulfoxaflor on gill cells was determined by measuring TBARS levels. The results of this study demonstrated that sulfoxaflor activated GSH related antioxidants by increasing tGSH levels, GPx, GR enzyme activities and by diminishing GST enzyme activity in the gill of zebrafish. Sulfoxaflor also caused oxidative damage in the gill of zebrafish by increasing lipid peroxidation. In conclusion, this study indicated that sulfoxaflor led to oxidative stress and activation of GSH related antioxidants in the gill of zebrafish. SAGE Publications 2021-06-28 /pmc/articles/PMC10454941/ /pubmed/34176341 http://dx.doi.org/10.1177/00368504211028361 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Article
Piner Benli, Petek
Çelik, Mehmet
Glutathione and its dependent enzymes’ modulatory responses to neonicotinoid insecticide sulfoxaflor induced oxidative damage in zebrafish in vivo
title Glutathione and its dependent enzymes’ modulatory responses to neonicotinoid insecticide sulfoxaflor induced oxidative damage in zebrafish in vivo
title_full Glutathione and its dependent enzymes’ modulatory responses to neonicotinoid insecticide sulfoxaflor induced oxidative damage in zebrafish in vivo
title_fullStr Glutathione and its dependent enzymes’ modulatory responses to neonicotinoid insecticide sulfoxaflor induced oxidative damage in zebrafish in vivo
title_full_unstemmed Glutathione and its dependent enzymes’ modulatory responses to neonicotinoid insecticide sulfoxaflor induced oxidative damage in zebrafish in vivo
title_short Glutathione and its dependent enzymes’ modulatory responses to neonicotinoid insecticide sulfoxaflor induced oxidative damage in zebrafish in vivo
title_sort glutathione and its dependent enzymes’ modulatory responses to neonicotinoid insecticide sulfoxaflor induced oxidative damage in zebrafish in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454941/
https://www.ncbi.nlm.nih.gov/pubmed/34176341
http://dx.doi.org/10.1177/00368504211028361
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