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The Impact of Preexisting Chronic Kidney Disease on the Severity and Recovery of Acute Kidney Injury

Authors
Lim, Sung YoonKo, Yoon SookLee, Hee YoungYang, Ji HyunKim, Myung GyuJo, Sang KyungCho, Won Yong
Issue Date
2018
Publisher
KARGER
Keywords
Acute kidney injury; Cell cycle arrest; Chronic kidney disease; Insulin-like growth factor-binding protein 7; Tissue inhibitor of metalloproteinase-2
Citation
NEPHRON, v.139, no.3, pp.254 - 268
Indexed
SCIE
SCOPUS
Journal Title
NEPHRON
Volume
139
Number
3
Start Page
254
End Page
268
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/80992
DOI
10.1159/000487492
ISSN
1660-8151
Abstract
Background: Recent observational studies have shown that in chronic kidney disease (CKD) patients, a significantly smaller percentage of patients with an episode of acute kidney injury (AKI) have full recovery of renal function compared to those without CKD. However, precise mechanisms involved in the incomplete repair after AKI with preexisting CKD have not been completely ascertained. Here, we assessed the impact of preexisting CKD on the severity and recovery of AKI in a mouse model of 5/6 nephrectomy. Methods: Male CD-1 mice underwent 5/6 nephrectomy (Nx). Six weeks post surgery, ischemia reperfusion injury (IRI) or a sham operation was performed and functional, histological, and various molecular parameters were compared between them. Results: Serum creatinine level on day 1 after IRI was comparable between control and Nx mice. However, serum creatinine remained significantly higher throughout the recovery phase in Nx mice compared to control mice. mRNA and protein expression of the cell cycle regulatory proteins were persistently elevated in Nx mice and this was associated with significantly increased levels of the G1 cell cycle arrest markers. Treatment with a p53 inhibitor following IRI resulted in not only decreased expression of G1 arrest markers but also decreased fibrosis, suggesting that prolonged epithelial G1 cell cycle arrest might be partially responsible for impaired recovery from superimposed AKI on CKD. Conclusion: Taken together, reduced nephron mass have a negative effect on the repair process that is partially mediated by the disruption of the cell cycle regulation. (C) 2018 S. Karger AG, Basel
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