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Virgin olive oil ameliorates deltamethrin-induced nephrotoxicity in mice: A biochemical and immunohistochemical assessment

OBJECTIVE: A major class of synthetic pyrethroid insecticide, deltamethrin (DM), can elicit pathophysiological effects through oxidative stress in non-targeted organisms such as mammals. There is accumulating evidence that virgin olive oil (VOO), a rich source of polyphenolic components, have anti-o...

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Autores principales: khalatbary, Ali Reza, Ahmadvand, Hassan, Ghabaee, Davood Nasiry Zarrin, Malekshah, Abbasali Karimpour, Navazesh, Azam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5616020/
https://www.ncbi.nlm.nih.gov/pubmed/28959581
http://dx.doi.org/10.1016/j.toxrep.2016.07.004
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author khalatbary, Ali Reza
Ahmadvand, Hassan
Ghabaee, Davood Nasiry Zarrin
Malekshah, Abbasali Karimpour
Navazesh, Azam
author_facet khalatbary, Ali Reza
Ahmadvand, Hassan
Ghabaee, Davood Nasiry Zarrin
Malekshah, Abbasali Karimpour
Navazesh, Azam
author_sort khalatbary, Ali Reza
collection PubMed
description OBJECTIVE: A major class of synthetic pyrethroid insecticide, deltamethrin (DM), can elicit pathophysiological effects through oxidative stress in non-targeted organisms such as mammals. There is accumulating evidence that virgin olive oil (VOO), a rich source of polyphenolic components, have anti-oxidant, anti-inflammatory, and anti-apoptotic properties. This study aimed to determine the protective and ameliorative effects of VOO against DM-induced nephrotoxicity. METHODS & MATERIALS: Mice were randomly divided into four equal groups: DM group, DM plus VOO group, VOO group, and vehicle group. Five weeks after gavaging, kidney samples were taken for biochemical assessment of malondialdehyde (MDA), glutathione (GSH) and catalase (CAT), and for immunohistochemical assessment of caspase-3, cyclooxygenase-2 (cox-2) and poly (ADP-ribose) polymerase (PARP). RESULTS: The MDA level in kidney was increased in the DM group, which was significantly decreased after VOO administration in the DM plus VOO group. The GSH level and CAT activiy in kidney were decreased in the DM group, which were significantly increased after VOO administration in the DM plus VOO group. Greater expression of caspase-3, cox-2, and PARP could be detected in the DM group, which was significantly attenuated in the DM plus VOO group. Also, the histopathological changes which were detected in the DM group attenuated after VOO consumption. CONCLUSION: Virgin olive oil exerted protective effects against deltamethrin-induced nephrotoxicity, which might be associated with its anti-apoptotic, anti-inflammatory, and anti-oxidative properties.
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spelling pubmed-56160202017-09-28 Virgin olive oil ameliorates deltamethrin-induced nephrotoxicity in mice: A biochemical and immunohistochemical assessment khalatbary, Ali Reza Ahmadvand, Hassan Ghabaee, Davood Nasiry Zarrin Malekshah, Abbasali Karimpour Navazesh, Azam Toxicol Rep Article OBJECTIVE: A major class of synthetic pyrethroid insecticide, deltamethrin (DM), can elicit pathophysiological effects through oxidative stress in non-targeted organisms such as mammals. There is accumulating evidence that virgin olive oil (VOO), a rich source of polyphenolic components, have anti-oxidant, anti-inflammatory, and anti-apoptotic properties. This study aimed to determine the protective and ameliorative effects of VOO against DM-induced nephrotoxicity. METHODS & MATERIALS: Mice were randomly divided into four equal groups: DM group, DM plus VOO group, VOO group, and vehicle group. Five weeks after gavaging, kidney samples were taken for biochemical assessment of malondialdehyde (MDA), glutathione (GSH) and catalase (CAT), and for immunohistochemical assessment of caspase-3, cyclooxygenase-2 (cox-2) and poly (ADP-ribose) polymerase (PARP). RESULTS: The MDA level in kidney was increased in the DM group, which was significantly decreased after VOO administration in the DM plus VOO group. The GSH level and CAT activiy in kidney were decreased in the DM group, which were significantly increased after VOO administration in the DM plus VOO group. Greater expression of caspase-3, cox-2, and PARP could be detected in the DM group, which was significantly attenuated in the DM plus VOO group. Also, the histopathological changes which were detected in the DM group attenuated after VOO consumption. CONCLUSION: Virgin olive oil exerted protective effects against deltamethrin-induced nephrotoxicity, which might be associated with its anti-apoptotic, anti-inflammatory, and anti-oxidative properties. Elsevier 2016-07-30 /pmc/articles/PMC5616020/ /pubmed/28959581 http://dx.doi.org/10.1016/j.toxrep.2016.07.004 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
khalatbary, Ali Reza
Ahmadvand, Hassan
Ghabaee, Davood Nasiry Zarrin
Malekshah, Abbasali Karimpour
Navazesh, Azam
Virgin olive oil ameliorates deltamethrin-induced nephrotoxicity in mice: A biochemical and immunohistochemical assessment
title Virgin olive oil ameliorates deltamethrin-induced nephrotoxicity in mice: A biochemical and immunohistochemical assessment
title_full Virgin olive oil ameliorates deltamethrin-induced nephrotoxicity in mice: A biochemical and immunohistochemical assessment
title_fullStr Virgin olive oil ameliorates deltamethrin-induced nephrotoxicity in mice: A biochemical and immunohistochemical assessment
title_full_unstemmed Virgin olive oil ameliorates deltamethrin-induced nephrotoxicity in mice: A biochemical and immunohistochemical assessment
title_short Virgin olive oil ameliorates deltamethrin-induced nephrotoxicity in mice: A biochemical and immunohistochemical assessment
title_sort virgin olive oil ameliorates deltamethrin-induced nephrotoxicity in mice: a biochemical and immunohistochemical assessment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5616020/
https://www.ncbi.nlm.nih.gov/pubmed/28959581
http://dx.doi.org/10.1016/j.toxrep.2016.07.004
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