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Resveratrol attenuates malathion-induced liver damage by reducing oxidative stress
BACKGROUND: Malathion is an organophosphate insecticide which disrupts the antioxidant system of the body. Resveratrol is a phytoestrogen and antioxidant of the red grape. AIM AND OBJECTIVE: This study was designed to evaluate the effects of resveratrol against toxic effects of malathion to the live...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771320/ https://www.ncbi.nlm.nih.gov/pubmed/31579256 http://dx.doi.org/10.4103/JLP.JLP_43_19 |
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author | Jalili, Cyrus Farzaei, Mohammad Hosein Roshankhah, Shiva Salahshoor, Mohammad Reza |
author_facet | Jalili, Cyrus Farzaei, Mohammad Hosein Roshankhah, Shiva Salahshoor, Mohammad Reza |
author_sort | Jalili, Cyrus |
collection | PubMed |
description | BACKGROUND: Malathion is an organophosphate insecticide which disrupts the antioxidant system of the body. Resveratrol is a phytoestrogen and antioxidant of the red grape. AIM AND OBJECTIVE: This study was designed to evaluate the effects of resveratrol against toxic effects of malathion to the liver of rats. MATERIALS AND METHODS: In this study, 48 male rats were randomly assigned to 8 groups: control normal (saline) and malathion control-treated groups (50 mg/kg), resveratrol groups (2, 8, and 20 mg/kg), and malathion + resveratrol-treated groups (2, 8, and 20 mg/kg). Treatments were administered intraperitoneally daily for 14 days. Griess technique was assessed for determined serum nitrite oxide level. Aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase concentrations were determined for liver functional disturbances. In addition, thiobarbituric acid reactive species, antioxidant capacity, the diameter of hepatocytes, and the central hepatic vein (CHV) were investigated. RESULTS: Malathion administration significantly improved liver malondialdehyde (MDA) and nitrite oxide level, the mean diameter of CHV and hepatocyte, and liver enzymes and decreased tissue ferric-reducing ability of plasma (FRAP) level compared to the normal control group (P < 0.01). The resveratrol and resveratrol + malathion treatments at all doses significantly reduced the mean diameter of hepatocyte and CHV, liver enzymes, kidney MDA, and nitrite oxide levels and increased tissue FRAP level compared to the malathion control group (P < 0.01). CONCLUSION: It seems that resveratrol administration improved liver injury induced by malathion in rats. |
format | Online Article Text |
id | pubmed-6771320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-67713202019-10-02 Resveratrol attenuates malathion-induced liver damage by reducing oxidative stress Jalili, Cyrus Farzaei, Mohammad Hosein Roshankhah, Shiva Salahshoor, Mohammad Reza J Lab Physicians Original Article BACKGROUND: Malathion is an organophosphate insecticide which disrupts the antioxidant system of the body. Resveratrol is a phytoestrogen and antioxidant of the red grape. AIM AND OBJECTIVE: This study was designed to evaluate the effects of resveratrol against toxic effects of malathion to the liver of rats. MATERIALS AND METHODS: In this study, 48 male rats were randomly assigned to 8 groups: control normal (saline) and malathion control-treated groups (50 mg/kg), resveratrol groups (2, 8, and 20 mg/kg), and malathion + resveratrol-treated groups (2, 8, and 20 mg/kg). Treatments were administered intraperitoneally daily for 14 days. Griess technique was assessed for determined serum nitrite oxide level. Aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase concentrations were determined for liver functional disturbances. In addition, thiobarbituric acid reactive species, antioxidant capacity, the diameter of hepatocytes, and the central hepatic vein (CHV) were investigated. RESULTS: Malathion administration significantly improved liver malondialdehyde (MDA) and nitrite oxide level, the mean diameter of CHV and hepatocyte, and liver enzymes and decreased tissue ferric-reducing ability of plasma (FRAP) level compared to the normal control group (P < 0.01). The resveratrol and resveratrol + malathion treatments at all doses significantly reduced the mean diameter of hepatocyte and CHV, liver enzymes, kidney MDA, and nitrite oxide levels and increased tissue FRAP level compared to the malathion control group (P < 0.01). CONCLUSION: It seems that resveratrol administration improved liver injury induced by malathion in rats. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6771320/ /pubmed/31579256 http://dx.doi.org/10.4103/JLP.JLP_43_19 Text en Copyright: © 2019 Journal of Laboratory Physicians http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Jalili, Cyrus Farzaei, Mohammad Hosein Roshankhah, Shiva Salahshoor, Mohammad Reza Resveratrol attenuates malathion-induced liver damage by reducing oxidative stress |
title | Resveratrol attenuates malathion-induced liver damage by reducing oxidative stress |
title_full | Resveratrol attenuates malathion-induced liver damage by reducing oxidative stress |
title_fullStr | Resveratrol attenuates malathion-induced liver damage by reducing oxidative stress |
title_full_unstemmed | Resveratrol attenuates malathion-induced liver damage by reducing oxidative stress |
title_short | Resveratrol attenuates malathion-induced liver damage by reducing oxidative stress |
title_sort | resveratrol attenuates malathion-induced liver damage by reducing oxidative stress |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771320/ https://www.ncbi.nlm.nih.gov/pubmed/31579256 http://dx.doi.org/10.4103/JLP.JLP_43_19 |
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