Localization of Klotho in cisplatin induced acute kidney failure.
10.14405/kjvr.2014.54.4.225
- Author:
So Ra PARK
1
;
Tae Won KIM
;
Young Jung KIM
;
Hyun Tae KIM
;
Si Yun RYU
;
Ju Young JUNG
Author Information
1. Department of Veterinary Medicine and Institute of Veterinary Science, Chungnam National University, Daejeon 305-764, Korea. jyjung@cnu.ac.kr
- Publication Type:Original Article
- Keywords:
acute kidney injury;
inflammatory cytokine;
Klotho;
localization
- MeSH:
Acute Kidney Injury*;
Animals;
Apoptosis;
Blotting, Western;
Cisplatin*;
Inflammation;
Injections, Intraperitoneal;
Kidney;
Necrosis;
NF-kappa B;
Rats;
Tumor Necrosis Factor-alpha
- From:Korean Journal of Veterinary Research
2014;54(4):225-231
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Klotho deficiency is an early event in acute kidney injury (AKI) that exacerbates acute kidney damage. The present study explored the expression of Klotho and inflammation related factors in cisplatin-induced AKI. Rats (n = 18) were treated with cisplatin intraperitoneal injection (5 mg/kg) or left untreated as controls (n = 6), then sacrificed at 5 (n = 6) and 10 days (n = 6) treatment. Five days after cisplatin injection, the serum kidney enzymes and kidney cell apoptosis were significantly increased. Moreover, the expression of Klotho was decreased when compared to the control group, especially in the cortex and outer medulla regions. In contrast, inflammation related signals including nuclear factor kappa B, tumor necrosis factor-alpha, and tumor necrosis factor-like weak inducer of apoptosis were enhanced. However, 10 days after cisplatin injection, Klotho expression was enhanced upon both IHC and Western blot analysis, with slightly recovered renal function and decreased apoptosis. Furthermore, inflammation related signals expression was decreased relative to the 5 days group. Overall, this study confirmed the opposite expression patterns between Klotho and inflammation related signals and their localization in cisplatin-induced AKI kidney.
