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Age-dependent changes in vancomycin-induced nephrotoxicity in mice

Vancomycin hydrochloride (VCM) is a glycopeptide antibiotic that is commonly used to eradicate methicillin-resistant gram-positive cocci, despite its nephrotoxic side effects. Elderly people are particularly susceptible to developing VCM-induced nephrotoxicity. However, the precise mechanism by whic...

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Autores principales: Takigawa, Masaki, Masutomi, Hirofumi, Shimazaki, Yoshitomo, Arai, Tomio, Lee, Jaewon, Ishii, Toshihiro, Mori, Yoshiko, Ishigami, Akihito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society of Toxicologic Pathology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361666/
https://www.ncbi.nlm.nih.gov/pubmed/30739996
http://dx.doi.org/10.1293/tox.2018-0036
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author Takigawa, Masaki
Masutomi, Hirofumi
Shimazaki, Yoshitomo
Arai, Tomio
Lee, Jaewon
Ishii, Toshihiro
Mori, Yoshiko
Ishigami, Akihito
author_facet Takigawa, Masaki
Masutomi, Hirofumi
Shimazaki, Yoshitomo
Arai, Tomio
Lee, Jaewon
Ishii, Toshihiro
Mori, Yoshiko
Ishigami, Akihito
author_sort Takigawa, Masaki
collection PubMed
description Vancomycin hydrochloride (VCM) is a glycopeptide antibiotic that is commonly used to eradicate methicillin-resistant gram-positive cocci, despite its nephrotoxic side effects. Elderly people are particularly susceptible to developing VCM-induced nephrotoxicity. However, the precise mechanism by which VCM induces nephrotoxicity in elderly people is not completely understood. Therefore, we investigated VCM-induced nephrotoxicity in mice of different ages. VCM was injected intraperitoneally into mice at 1, 3, 6, 12, and 24 months of age at a dosage of 400 mg/kg body weight for 3 and 14 days. Twenty-four hours after the last injection, we examined plasma creatinine levels and histopathological alterations in the kidneys. VCM administration increased plasma creatinine levels, and these values gradually increased to higher levels with aging. The histological examination revealed renal tubular degeneration, such as brush-border atrophy, apoptosis/necrosis of the tubular epithelium, and epithelial desquamation, that gradually became more severe with aging. Furthermore, immunohistochemical staining with anti-CD10 and anti-single-stranded DNA antibodies revealed damaged renal proximal tubules with marked dilatation, as well as numerous apoptotic cells, and these features increased in severity in 12- and 24-month-old mice receiving VCM. Based on these results, aged mice were highly susceptible to kidney damage induced by VCM administration. In addition, proximal tubular epithelial cells likely underwent apoptosis after the administration of VCM. This report is the first to document VCM-induced nephrotoxicity in mice of different ages. Thus, this mouse model could be useful for understanding the mechanisms of VCM-induced nephrotoxicity in the elderly.
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spelling pubmed-63616662019-02-08 Age-dependent changes in vancomycin-induced nephrotoxicity in mice Takigawa, Masaki Masutomi, Hirofumi Shimazaki, Yoshitomo Arai, Tomio Lee, Jaewon Ishii, Toshihiro Mori, Yoshiko Ishigami, Akihito J Toxicol Pathol Original Article Vancomycin hydrochloride (VCM) is a glycopeptide antibiotic that is commonly used to eradicate methicillin-resistant gram-positive cocci, despite its nephrotoxic side effects. Elderly people are particularly susceptible to developing VCM-induced nephrotoxicity. However, the precise mechanism by which VCM induces nephrotoxicity in elderly people is not completely understood. Therefore, we investigated VCM-induced nephrotoxicity in mice of different ages. VCM was injected intraperitoneally into mice at 1, 3, 6, 12, and 24 months of age at a dosage of 400 mg/kg body weight for 3 and 14 days. Twenty-four hours after the last injection, we examined plasma creatinine levels and histopathological alterations in the kidneys. VCM administration increased plasma creatinine levels, and these values gradually increased to higher levels with aging. The histological examination revealed renal tubular degeneration, such as brush-border atrophy, apoptosis/necrosis of the tubular epithelium, and epithelial desquamation, that gradually became more severe with aging. Furthermore, immunohistochemical staining with anti-CD10 and anti-single-stranded DNA antibodies revealed damaged renal proximal tubules with marked dilatation, as well as numerous apoptotic cells, and these features increased in severity in 12- and 24-month-old mice receiving VCM. Based on these results, aged mice were highly susceptible to kidney damage induced by VCM administration. In addition, proximal tubular epithelial cells likely underwent apoptosis after the administration of VCM. This report is the first to document VCM-induced nephrotoxicity in mice of different ages. Thus, this mouse model could be useful for understanding the mechanisms of VCM-induced nephrotoxicity in the elderly. Japanese Society of Toxicologic Pathology 2018-12-10 2019-01 /pmc/articles/PMC6361666/ /pubmed/30739996 http://dx.doi.org/10.1293/tox.2018-0036 Text en ©2019 The Japanese Society of Toxicologic Pathology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Takigawa, Masaki
Masutomi, Hirofumi
Shimazaki, Yoshitomo
Arai, Tomio
Lee, Jaewon
Ishii, Toshihiro
Mori, Yoshiko
Ishigami, Akihito
Age-dependent changes in vancomycin-induced nephrotoxicity in mice
title Age-dependent changes in vancomycin-induced nephrotoxicity in mice
title_full Age-dependent changes in vancomycin-induced nephrotoxicity in mice
title_fullStr Age-dependent changes in vancomycin-induced nephrotoxicity in mice
title_full_unstemmed Age-dependent changes in vancomycin-induced nephrotoxicity in mice
title_short Age-dependent changes in vancomycin-induced nephrotoxicity in mice
title_sort age-dependent changes in vancomycin-induced nephrotoxicity in mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361666/
https://www.ncbi.nlm.nih.gov/pubmed/30739996
http://dx.doi.org/10.1293/tox.2018-0036
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