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Ameliorative effect of virgin olive oil against nephrotoxicity following sub-chronic administration of ethephon in male rats
BACKGROUND: Ethephon (EP) is the most famous plant growth regulator with different adverse effects on kidney function. Virgin Olive Oil (VOO) is considered as a natural source of antioxidant with beneficial effects. Thus, this study was conducted to investigate the effects of VOO on nephrotoxicity i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484965/ https://www.ncbi.nlm.nih.gov/pubmed/32953565 http://dx.doi.org/10.1016/j.jtcme.2019.08.005 |
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author | Mokhtari, Tahmineh Hussein Osman, Hosam-Eldin El-Meghawry El-Kenawy, Ayman Dashti, Nasrin |
author_facet | Mokhtari, Tahmineh Hussein Osman, Hosam-Eldin El-Meghawry El-Kenawy, Ayman Dashti, Nasrin |
author_sort | Mokhtari, Tahmineh |
collection | PubMed |
description | BACKGROUND: Ethephon (EP) is the most famous plant growth regulator with different adverse effects on kidney function. Virgin Olive Oil (VOO) is considered as a natural source of antioxidant with beneficial effects. Thus, this study was conducted to investigate the effects of VOO on nephrotoxicity induced by EP in rats. METHODS AND MATERIALS: In this study, 80 male rats (weighing 200–250 g) were divided into four groups including I: control group received normal saline as vehicle, II: received VOO, III: received EP (150 mg/kg/day) for 2 months, IV: received EP (150 mg/kg/day for 2 months, after 2-month pretreatment with VOO. VOO (2 mL/kg/day) and vehicle were administered by gastric gavage for 2 months. At the end, the animals were sacrificed, and their blood and kidneys were used for examinations. Isolated kidneys were used for histopathological and oxidative stress studies. RESULTS: Significant increases were recorded in blood (neutrophils, monocytes) and urinary parameters as well as malondialdehyde (MDA) content in the group III compared to groups II and I (P˂0.05). Antioxidant enzymes significantly declined and histopathological alterations increased in the group III. In the group IV, significant decreases were recorded in blood and urinary parameters, MDA, and histopathological alterations and a significant increase were found in antioxidant enzymes compared to group III (P˂0.05). CONCLUSIONS: Findings of the present study demonstrated protective effects of VOO in prevention of kidneys against EP -induced toxicity in albino rats. |
format | Online Article Text |
id | pubmed-7484965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-74849652020-09-17 Ameliorative effect of virgin olive oil against nephrotoxicity following sub-chronic administration of ethephon in male rats Mokhtari, Tahmineh Hussein Osman, Hosam-Eldin El-Meghawry El-Kenawy, Ayman Dashti, Nasrin J Tradit Complement Med Original Article BACKGROUND: Ethephon (EP) is the most famous plant growth regulator with different adverse effects on kidney function. Virgin Olive Oil (VOO) is considered as a natural source of antioxidant with beneficial effects. Thus, this study was conducted to investigate the effects of VOO on nephrotoxicity induced by EP in rats. METHODS AND MATERIALS: In this study, 80 male rats (weighing 200–250 g) were divided into four groups including I: control group received normal saline as vehicle, II: received VOO, III: received EP (150 mg/kg/day) for 2 months, IV: received EP (150 mg/kg/day for 2 months, after 2-month pretreatment with VOO. VOO (2 mL/kg/day) and vehicle were administered by gastric gavage for 2 months. At the end, the animals were sacrificed, and their blood and kidneys were used for examinations. Isolated kidneys were used for histopathological and oxidative stress studies. RESULTS: Significant increases were recorded in blood (neutrophils, monocytes) and urinary parameters as well as malondialdehyde (MDA) content in the group III compared to groups II and I (P˂0.05). Antioxidant enzymes significantly declined and histopathological alterations increased in the group III. In the group IV, significant decreases were recorded in blood and urinary parameters, MDA, and histopathological alterations and a significant increase were found in antioxidant enzymes compared to group III (P˂0.05). CONCLUSIONS: Findings of the present study demonstrated protective effects of VOO in prevention of kidneys against EP -induced toxicity in albino rats. Elsevier 2019-08-28 /pmc/articles/PMC7484965/ /pubmed/32953565 http://dx.doi.org/10.1016/j.jtcme.2019.08.005 Text en © 2019 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Mokhtari, Tahmineh Hussein Osman, Hosam-Eldin El-Meghawry El-Kenawy, Ayman Dashti, Nasrin Ameliorative effect of virgin olive oil against nephrotoxicity following sub-chronic administration of ethephon in male rats |
title | Ameliorative effect of virgin olive oil against nephrotoxicity following sub-chronic administration of ethephon in male rats |
title_full | Ameliorative effect of virgin olive oil against nephrotoxicity following sub-chronic administration of ethephon in male rats |
title_fullStr | Ameliorative effect of virgin olive oil against nephrotoxicity following sub-chronic administration of ethephon in male rats |
title_full_unstemmed | Ameliorative effect of virgin olive oil against nephrotoxicity following sub-chronic administration of ethephon in male rats |
title_short | Ameliorative effect of virgin olive oil against nephrotoxicity following sub-chronic administration of ethephon in male rats |
title_sort | ameliorative effect of virgin olive oil against nephrotoxicity following sub-chronic administration of ethephon in male rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484965/ https://www.ncbi.nlm.nih.gov/pubmed/32953565 http://dx.doi.org/10.1016/j.jtcme.2019.08.005 |
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