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Liver δ-Aminolevulinate Dehydratase Activity is Inhibited by Neonicotinoids and Restored by Antioxidant Agents
Neonicotinoids represent the most used class of insecticides worldwide, and their precursor, imidacloprid, is the most widely marketed. The aim of this study was to evaluate the effect of imidacloprid on the activity of hepatic δ-aminolevulinate dehydratase (δ-ALA-D), protective effect of potential...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245637/ https://www.ncbi.nlm.nih.gov/pubmed/25402564 http://dx.doi.org/10.3390/ijerph111111676 |
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author | Sauer, Elisa Moro, Angela M. Brucker, Natália Nascimento, Sabrina Gauer, Bruna Fracasso, Rafael Gioda, Adriana Beck, Ruy Moreira, José C. F. Eifler-Lima, Vera Lucia Garcia, Solange Cristina |
author_facet | Sauer, Elisa Moro, Angela M. Brucker, Natália Nascimento, Sabrina Gauer, Bruna Fracasso, Rafael Gioda, Adriana Beck, Ruy Moreira, José C. F. Eifler-Lima, Vera Lucia Garcia, Solange Cristina |
author_sort | Sauer, Elisa |
collection | PubMed |
description | Neonicotinoids represent the most used class of insecticides worldwide, and their precursor, imidacloprid, is the most widely marketed. The aim of this study was to evaluate the effect of imidacloprid on the activity of hepatic δ-aminolevulinate dehydratase (δ-ALA-D), protective effect of potential antioxidants against this potential effect and presence of chemical elements in the constitution of this pesticide. We observed that δ-ALA-D activity was significantly inhibited by imidacloprid at all concentrations tested in a dose-dependent manner. The IC(50) value was obtained and used to evaluate the restoration of the enzymatic activity. δ-ALA-D inhibition was completely restored by addition of dithiotreitol (DTT) and partly by ZnCl(2,) demonstrating that the inhibition occurs by oxidation of thiol groups and by displacement of the Zn (II), which can be explained by the presence of chemical elements found in the constitution of pesticides. Reduced glutathione (GSH) had the best antioxidant effect against to δ-ALA-D inhibition caused by imidacloprid, followed by curcumin and resveratrol. It is well known that inhibition of the enzyme δ-ALA-D may result in accumulation of its neurotoxic substrate (δ-ALA), in this line, our results suggest that further studies are needed to investigate the possible neurotoxicity induced by neonicotinoids and the involvement of antioxidants in cases of poisoning by neonicotinoids. |
format | Online Article Text |
id | pubmed-4245637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-42456372014-12-02 Liver δ-Aminolevulinate Dehydratase Activity is Inhibited by Neonicotinoids and Restored by Antioxidant Agents Sauer, Elisa Moro, Angela M. Brucker, Natália Nascimento, Sabrina Gauer, Bruna Fracasso, Rafael Gioda, Adriana Beck, Ruy Moreira, José C. F. Eifler-Lima, Vera Lucia Garcia, Solange Cristina Int J Environ Res Public Health Article Neonicotinoids represent the most used class of insecticides worldwide, and their precursor, imidacloprid, is the most widely marketed. The aim of this study was to evaluate the effect of imidacloprid on the activity of hepatic δ-aminolevulinate dehydratase (δ-ALA-D), protective effect of potential antioxidants against this potential effect and presence of chemical elements in the constitution of this pesticide. We observed that δ-ALA-D activity was significantly inhibited by imidacloprid at all concentrations tested in a dose-dependent manner. The IC(50) value was obtained and used to evaluate the restoration of the enzymatic activity. δ-ALA-D inhibition was completely restored by addition of dithiotreitol (DTT) and partly by ZnCl(2,) demonstrating that the inhibition occurs by oxidation of thiol groups and by displacement of the Zn (II), which can be explained by the presence of chemical elements found in the constitution of pesticides. Reduced glutathione (GSH) had the best antioxidant effect against to δ-ALA-D inhibition caused by imidacloprid, followed by curcumin and resveratrol. It is well known that inhibition of the enzyme δ-ALA-D may result in accumulation of its neurotoxic substrate (δ-ALA), in this line, our results suggest that further studies are needed to investigate the possible neurotoxicity induced by neonicotinoids and the involvement of antioxidants in cases of poisoning by neonicotinoids. MDPI 2014-11-13 2014-11 /pmc/articles/PMC4245637/ /pubmed/25402564 http://dx.doi.org/10.3390/ijerph111111676 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sauer, Elisa Moro, Angela M. Brucker, Natália Nascimento, Sabrina Gauer, Bruna Fracasso, Rafael Gioda, Adriana Beck, Ruy Moreira, José C. F. Eifler-Lima, Vera Lucia Garcia, Solange Cristina Liver δ-Aminolevulinate Dehydratase Activity is Inhibited by Neonicotinoids and Restored by Antioxidant Agents |
title | Liver δ-Aminolevulinate Dehydratase Activity is Inhibited by Neonicotinoids and Restored by Antioxidant Agents |
title_full | Liver δ-Aminolevulinate Dehydratase Activity is Inhibited by Neonicotinoids and Restored by Antioxidant Agents |
title_fullStr | Liver δ-Aminolevulinate Dehydratase Activity is Inhibited by Neonicotinoids and Restored by Antioxidant Agents |
title_full_unstemmed | Liver δ-Aminolevulinate Dehydratase Activity is Inhibited by Neonicotinoids and Restored by Antioxidant Agents |
title_short | Liver δ-Aminolevulinate Dehydratase Activity is Inhibited by Neonicotinoids and Restored by Antioxidant Agents |
title_sort | liver δ-aminolevulinate dehydratase activity is inhibited by neonicotinoids and restored by antioxidant agents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4245637/ https://www.ncbi.nlm.nih.gov/pubmed/25402564 http://dx.doi.org/10.3390/ijerph111111676 |
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