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The Combined Administration of Vitamin C and Copper Induces a Systemic Oxidative Stress and Kidney Injury

Vitamin C (ascorbic acid; AA) and copper (Cu(2+)) are well used supplements with many health-promoting actions. However, when they are used in combination, the Fenton reaction occurs, leading to the formation of highly reactive hydroxyl radicals. Given that kidney is vulnerable to many toxicants inc...

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Autores principales: Jiang, Rui, Sui, Yang, Hong, Jingru, Niimi, Manabu, Yan, Qiaojing, Shi, Zhuheng, Yao, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9856059/
https://www.ncbi.nlm.nih.gov/pubmed/36671529
http://dx.doi.org/10.3390/biom13010143
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author Jiang, Rui
Sui, Yang
Hong, Jingru
Niimi, Manabu
Yan, Qiaojing
Shi, Zhuheng
Yao, Jian
author_facet Jiang, Rui
Sui, Yang
Hong, Jingru
Niimi, Manabu
Yan, Qiaojing
Shi, Zhuheng
Yao, Jian
author_sort Jiang, Rui
collection PubMed
description Vitamin C (ascorbic acid; AA) and copper (Cu(2+)) are well used supplements with many health-promoting actions. However, when they are used in combination, the Fenton reaction occurs, leading to the formation of highly reactive hydroxyl radicals. Given that kidney is vulnerable to many toxicants including free radicals, we speculated that the in vivo administration of AA plus Cu(2+) may cause oxidative kidney injury. The purpose of this study was to address this possibility. Mice were administered with AA and Cu(2+), alone or in combination, via oral gavage once a day for various periods. Changes in the systemic oxidative status, as well renal structure and functions, were examined. The administration of AA plus Cu(2+) elevated protein oxidation in serum, intestine, bladder, and kidney, as evidenced by the increased sulfenic acid formation and decreased level of free sulfhydryl groups (-SH). The systemic oxidative stress induced by AA plus Cu(2+) was associated with a significant loss of renal function and structure, as indicated by the increased blood urea nitrogen (BUN), creatinine and urinary proteins, as well as glomerular and tubular cell injury. These effects of AA and Cu(2+) were only observed when used in combination, and could be entirely prevented by thiol antioxidant NAC. Further analysis using cultured renal tubular epithelial cells revealed that AA plus Cu(2+) caused cellular protein oxidation and cell death, which could be abolished by NAC and catalase. Moreover, coincubation of AA and Cu(2+) led to H(2)O(2) production. Collectively, our study revealed that a combined administration of AA and Cu(2+) resulted in systemic oxidative stress and renal cell injury. As health-promoting supplements, AA and Cu(2+) should not be used together.
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spelling pubmed-98560592023-01-21 The Combined Administration of Vitamin C and Copper Induces a Systemic Oxidative Stress and Kidney Injury Jiang, Rui Sui, Yang Hong, Jingru Niimi, Manabu Yan, Qiaojing Shi, Zhuheng Yao, Jian Biomolecules Article Vitamin C (ascorbic acid; AA) and copper (Cu(2+)) are well used supplements with many health-promoting actions. However, when they are used in combination, the Fenton reaction occurs, leading to the formation of highly reactive hydroxyl radicals. Given that kidney is vulnerable to many toxicants including free radicals, we speculated that the in vivo administration of AA plus Cu(2+) may cause oxidative kidney injury. The purpose of this study was to address this possibility. Mice were administered with AA and Cu(2+), alone or in combination, via oral gavage once a day for various periods. Changes in the systemic oxidative status, as well renal structure and functions, were examined. The administration of AA plus Cu(2+) elevated protein oxidation in serum, intestine, bladder, and kidney, as evidenced by the increased sulfenic acid formation and decreased level of free sulfhydryl groups (-SH). The systemic oxidative stress induced by AA plus Cu(2+) was associated with a significant loss of renal function and structure, as indicated by the increased blood urea nitrogen (BUN), creatinine and urinary proteins, as well as glomerular and tubular cell injury. These effects of AA and Cu(2+) were only observed when used in combination, and could be entirely prevented by thiol antioxidant NAC. Further analysis using cultured renal tubular epithelial cells revealed that AA plus Cu(2+) caused cellular protein oxidation and cell death, which could be abolished by NAC and catalase. Moreover, coincubation of AA and Cu(2+) led to H(2)O(2) production. Collectively, our study revealed that a combined administration of AA and Cu(2+) resulted in systemic oxidative stress and renal cell injury. As health-promoting supplements, AA and Cu(2+) should not be used together. MDPI 2023-01-10 /pmc/articles/PMC9856059/ /pubmed/36671529 http://dx.doi.org/10.3390/biom13010143 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jiang, Rui
Sui, Yang
Hong, Jingru
Niimi, Manabu
Yan, Qiaojing
Shi, Zhuheng
Yao, Jian
The Combined Administration of Vitamin C and Copper Induces a Systemic Oxidative Stress and Kidney Injury
title The Combined Administration of Vitamin C and Copper Induces a Systemic Oxidative Stress and Kidney Injury
title_full The Combined Administration of Vitamin C and Copper Induces a Systemic Oxidative Stress and Kidney Injury
title_fullStr The Combined Administration of Vitamin C and Copper Induces a Systemic Oxidative Stress and Kidney Injury
title_full_unstemmed The Combined Administration of Vitamin C and Copper Induces a Systemic Oxidative Stress and Kidney Injury
title_short The Combined Administration of Vitamin C and Copper Induces a Systemic Oxidative Stress and Kidney Injury
title_sort combined administration of vitamin c and copper induces a systemic oxidative stress and kidney injury
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9856059/
https://www.ncbi.nlm.nih.gov/pubmed/36671529
http://dx.doi.org/10.3390/biom13010143
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