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Protective effects of vitamin D(3) (cholecalciferol) on vancomycin-induced oxidative nephrotoxic damage in rats

CONTEXT: Vancomycin (VCM), an important antibiotic against refractory infections, has been used to treat secondary infections in severe COVID-19 patients. Regrettably, VCM treatment has been associated with nephrotoxicity. Vitamin D(3) can prevent nephrotoxicity through its antioxidant effect. OBJEC...

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Autores principales: Al-Sroji, Rouba Yasser, Al-Laham, Shaza, Almandili, Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161947/
https://www.ncbi.nlm.nih.gov/pubmed/37139624
http://dx.doi.org/10.1080/13880209.2023.2204916
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author Al-Sroji, Rouba Yasser
Al-Laham, Shaza
Almandili, Ahmad
author_facet Al-Sroji, Rouba Yasser
Al-Laham, Shaza
Almandili, Ahmad
author_sort Al-Sroji, Rouba Yasser
collection PubMed
description CONTEXT: Vancomycin (VCM), an important antibiotic against refractory infections, has been used to treat secondary infections in severe COVID-19 patients. Regrettably, VCM treatment has been associated with nephrotoxicity. Vitamin D(3) can prevent nephrotoxicity through its antioxidant effect. OBJECTIVE: This study tests the antioxidant effect of vitamin D(3) in the prevention of VCM-induced nephrotoxicity. MATERIALS AND METHODS: Wistar Albino rats (21) were randomly divided into 3 groups: (A) control; (B) VCM 300 mg/kg daily for 1 week; and (C) VCM plus vitamin D(3) 500 IU/kg daily for 2 weeks. All the rats were sacrificed and serum was separated to determine kidney function parameters. Their kidneys were also dissected for histological examination and for oxidative stress markers. RESULTS: Lipid peroxidation, creatinine, and urea levels decreased significantly (p < 0.0001) in the vitamin D(3)-treated group (14.46, 84.11, 36.17%, respectively) compared to the VCM group that was given VCM (MIC<2 μg/mL) only. A significant increase was observed in superoxide dismutase levels in the vitamin D(3)-treated group (p < 0.05) compared to rats without treatment. Furthermore, kidney histopathology of the rats treated with vitamin D(3) showed that dilatation, vacuolization and necrosis tubules decreased significantly (p < 0.05) compared with those in the VCM group. Glomerular injury, hyaline dystrophy, and inflammation improved significantly in the vitamin D(3) group (p < 0.001, p < 0.05, p < 0.05, respectively) compared with the VCM group. DISCUSSION AND CONCLUSIONS: Vitamin D(3) can prevent VCM nephrotoxicity. Therefore, the appropriate dose of this vitamin must be determined, especially for those infected with COVID-19 and receiving VCM, to manage their secondary infections.
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spelling pubmed-101619472023-05-06 Protective effects of vitamin D(3) (cholecalciferol) on vancomycin-induced oxidative nephrotoxic damage in rats Al-Sroji, Rouba Yasser Al-Laham, Shaza Almandili, Ahmad Pharm Biol Research Article CONTEXT: Vancomycin (VCM), an important antibiotic against refractory infections, has been used to treat secondary infections in severe COVID-19 patients. Regrettably, VCM treatment has been associated with nephrotoxicity. Vitamin D(3) can prevent nephrotoxicity through its antioxidant effect. OBJECTIVE: This study tests the antioxidant effect of vitamin D(3) in the prevention of VCM-induced nephrotoxicity. MATERIALS AND METHODS: Wistar Albino rats (21) were randomly divided into 3 groups: (A) control; (B) VCM 300 mg/kg daily for 1 week; and (C) VCM plus vitamin D(3) 500 IU/kg daily for 2 weeks. All the rats were sacrificed and serum was separated to determine kidney function parameters. Their kidneys were also dissected for histological examination and for oxidative stress markers. RESULTS: Lipid peroxidation, creatinine, and urea levels decreased significantly (p < 0.0001) in the vitamin D(3)-treated group (14.46, 84.11, 36.17%, respectively) compared to the VCM group that was given VCM (MIC<2 μg/mL) only. A significant increase was observed in superoxide dismutase levels in the vitamin D(3)-treated group (p < 0.05) compared to rats without treatment. Furthermore, kidney histopathology of the rats treated with vitamin D(3) showed that dilatation, vacuolization and necrosis tubules decreased significantly (p < 0.05) compared with those in the VCM group. Glomerular injury, hyaline dystrophy, and inflammation improved significantly in the vitamin D(3) group (p < 0.001, p < 0.05, p < 0.05, respectively) compared with the VCM group. DISCUSSION AND CONCLUSIONS: Vitamin D(3) can prevent VCM nephrotoxicity. Therefore, the appropriate dose of this vitamin must be determined, especially for those infected with COVID-19 and receiving VCM, to manage their secondary infections. Taylor & Francis 2023-05-04 /pmc/articles/PMC10161947/ /pubmed/37139624 http://dx.doi.org/10.1080/13880209.2023.2204916 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Article
Al-Sroji, Rouba Yasser
Al-Laham, Shaza
Almandili, Ahmad
Protective effects of vitamin D(3) (cholecalciferol) on vancomycin-induced oxidative nephrotoxic damage in rats
title Protective effects of vitamin D(3) (cholecalciferol) on vancomycin-induced oxidative nephrotoxic damage in rats
title_full Protective effects of vitamin D(3) (cholecalciferol) on vancomycin-induced oxidative nephrotoxic damage in rats
title_fullStr Protective effects of vitamin D(3) (cholecalciferol) on vancomycin-induced oxidative nephrotoxic damage in rats
title_full_unstemmed Protective effects of vitamin D(3) (cholecalciferol) on vancomycin-induced oxidative nephrotoxic damage in rats
title_short Protective effects of vitamin D(3) (cholecalciferol) on vancomycin-induced oxidative nephrotoxic damage in rats
title_sort protective effects of vitamin d(3) (cholecalciferol) on vancomycin-induced oxidative nephrotoxic damage in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161947/
https://www.ncbi.nlm.nih.gov/pubmed/37139624
http://dx.doi.org/10.1080/13880209.2023.2204916
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