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Falcaria vulgaris L. hydroalcoholic extract protects against harmful effects of mercuric chloride on the rat kidney

OBJECTIVE: Mercuric chloride (Merc; HgCl(2)) is toxic to humans and animals and contributes to environmental pollution, which usually results in nerve and systemic harm to different organs. Falcaria vulgaris (FV) is a medicinal plant rich in antioxidants. This research aimed to assess the FV hydroal...

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Autores principales: Ghanbari, Ali, Jalili, Cyrus, Abdolmaleki, Amir, Zhaleh, Mohsen, Zarinkhat, Armin, Akhshi, Nasim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474913/
https://www.ncbi.nlm.nih.gov/pubmed/37663383
http://dx.doi.org/10.22038/AJP.2023.21872
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author Ghanbari, Ali
Jalili, Cyrus
Abdolmaleki, Amir
Zhaleh, Mohsen
Zarinkhat, Armin
Akhshi, Nasim
author_facet Ghanbari, Ali
Jalili, Cyrus
Abdolmaleki, Amir
Zhaleh, Mohsen
Zarinkhat, Armin
Akhshi, Nasim
author_sort Ghanbari, Ali
collection PubMed
description OBJECTIVE: Mercuric chloride (Merc; HgCl(2)) is toxic to humans and animals and contributes to environmental pollution, which usually results in nerve and systemic harm to different organs. Falcaria vulgaris (FV) is a medicinal plant rich in antioxidants. This research aimed to assess the FV hydroalcoholic extract effects on kidney toxicity induced by Merc. MATERIALS AND METHODS: Forty-eight male rats were divided into eight groups: the control group: received saline; the Merc group: received 0.5 ml/day of 0.5 ppm aqueous Merc; FV1, 2, and 3 groups: received 50, 100, 150 mg/kg FV, respectively; and Merc + FV1, 2, and 3 groups: received Merc and FV at three doses. The administration period was 14-days. Subsequently, kidneys and sera were cumulated from each group for the analysis. Samples were analyzed via hematoxylin-eosin staining and biochemical tests. RESULTS: The rats that received Merc displayed significant decrement in the kidney index, the diameter of renal corpuscles, total antioxidant capacity levels, superoxide dismutase activity (all, p<0.01), and 150 mg/kg FV mitigated these outcomes (all, p<0.05). Urea, creatinine, nitric oxide, and the level of apoptosis revealed a significant increment in the kidney of the rats that received Merc (all, p<0.01), and 150 mg/kg FV decreased these results. Furthermore, FV ameliorated histological changes induced by Merc (all, p<0.05). CONCLUSION: The FV hydroalcoholic extract protects the kidneys against Merc-induced nephrotoxicity. Antioxidant and anti-apoptotic FV hydroalcoholic extract properties were involved in this healing effect.
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spelling pubmed-104749132023-09-03 Falcaria vulgaris L. hydroalcoholic extract protects against harmful effects of mercuric chloride on the rat kidney Ghanbari, Ali Jalili, Cyrus Abdolmaleki, Amir Zhaleh, Mohsen Zarinkhat, Armin Akhshi, Nasim Avicenna J Phytomed Original Research Article OBJECTIVE: Mercuric chloride (Merc; HgCl(2)) is toxic to humans and animals and contributes to environmental pollution, which usually results in nerve and systemic harm to different organs. Falcaria vulgaris (FV) is a medicinal plant rich in antioxidants. This research aimed to assess the FV hydroalcoholic extract effects on kidney toxicity induced by Merc. MATERIALS AND METHODS: Forty-eight male rats were divided into eight groups: the control group: received saline; the Merc group: received 0.5 ml/day of 0.5 ppm aqueous Merc; FV1, 2, and 3 groups: received 50, 100, 150 mg/kg FV, respectively; and Merc + FV1, 2, and 3 groups: received Merc and FV at three doses. The administration period was 14-days. Subsequently, kidneys and sera were cumulated from each group for the analysis. Samples were analyzed via hematoxylin-eosin staining and biochemical tests. RESULTS: The rats that received Merc displayed significant decrement in the kidney index, the diameter of renal corpuscles, total antioxidant capacity levels, superoxide dismutase activity (all, p<0.01), and 150 mg/kg FV mitigated these outcomes (all, p<0.05). Urea, creatinine, nitric oxide, and the level of apoptosis revealed a significant increment in the kidney of the rats that received Merc (all, p<0.01), and 150 mg/kg FV decreased these results. Furthermore, FV ameliorated histological changes induced by Merc (all, p<0.05). CONCLUSION: The FV hydroalcoholic extract protects the kidneys against Merc-induced nephrotoxicity. Antioxidant and anti-apoptotic FV hydroalcoholic extract properties were involved in this healing effect. Mashhad University of Medical Sciences 2023 /pmc/articles/PMC10474913/ /pubmed/37663383 http://dx.doi.org/10.22038/AJP.2023.21872 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Ghanbari, Ali
Jalili, Cyrus
Abdolmaleki, Amir
Zhaleh, Mohsen
Zarinkhat, Armin
Akhshi, Nasim
Falcaria vulgaris L. hydroalcoholic extract protects against harmful effects of mercuric chloride on the rat kidney
title Falcaria vulgaris L. hydroalcoholic extract protects against harmful effects of mercuric chloride on the rat kidney
title_full Falcaria vulgaris L. hydroalcoholic extract protects against harmful effects of mercuric chloride on the rat kidney
title_fullStr Falcaria vulgaris L. hydroalcoholic extract protects against harmful effects of mercuric chloride on the rat kidney
title_full_unstemmed Falcaria vulgaris L. hydroalcoholic extract protects against harmful effects of mercuric chloride on the rat kidney
title_short Falcaria vulgaris L. hydroalcoholic extract protects against harmful effects of mercuric chloride on the rat kidney
title_sort falcaria vulgaris l. hydroalcoholic extract protects against harmful effects of mercuric chloride on the rat kidney
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474913/
https://www.ncbi.nlm.nih.gov/pubmed/37663383
http://dx.doi.org/10.22038/AJP.2023.21872
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