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Age-dependent changes in vancomycin-induced nephrotoxicity in mice
Masaki Takigawa1,2, Hirofumi Masutomi1, Yoshitomo Shimazaki1,2
1Molecular Regulation of Aging, Tokyo Metropolitan Institute of Gerontology, 35-2 Sakae-cho, Itabashi-ku, Tokyo 173-0015, Japan.
Abstract:
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.
Insights
Vancomycin (VCM) causes kidney damage, particularly in older individuals. Aged mice showed increased susceptibility to VCM-induced nephrotoxicity, with proximal tubular cells undergoing apoptosis, highlighting a potential model for elderly kidney injury.
Area of Science:
- Nephrology
- Pharmacology
- Gerontology
Background:
- Vancomycin hydrochloride (VCM) is crucial for treating resistant gram-positive infections.
- VCM-induced nephrotoxicity is a significant concern, especially in the elderly.
- The exact mechanisms of VCM nephrotoxicity in aging populations remain unclear.
Purpose of the Study:
- To investigate the impact of VCM on kidney function and structure across different ages in a mouse model.
- To elucidate the age-dependent susceptibility to VCM-induced nephrotoxicity.
- To identify potential cellular mechanisms underlying VCM nephrotoxicity in aged individuals.
Main Methods:
- Intraperitoneal injection of VCM (400 mg/kg) into mice aged 1, 3, 6, 12, and 24 months for 3 or 14 days.
- Assessment of plasma creatinine levels post-VCM administration.
- Histopathological and immunohistochemical analysis of kidney tissues, including evaluation of tubular degeneration and apoptosis.
Main Results:
- VCM administration significantly elevated plasma creatinine levels, with a progressive increase observed with aging.
- Histological examination revealed age-dependent worsening of renal tubular damage, including brush-border atrophy, tubular cell apoptosis/necrosis, and desquamation.
- Immunohistochemistry confirmed increased proximal tubule damage and apoptosis in aged mice treated with VCM.
Conclusions:
- Aged mice exhibit heightened susceptibility to VCM-induced nephrotoxicity.
- Apoptosis of proximal tubular epithelial cells is a key mechanism in VCM-induced kidney damage.
- This study establishes a valuable mouse model for investigating VCM nephrotoxicity in the elderly.
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