Caveolin-2 in urine as a novel biomarker of renal recovery after cisplatin induced nephrotoxicity in rats

被引:4
作者
Bulacio, Romina P. [1 ]
Torres, Adriana M. [1 ]
机构
[1] Univ Nacl Rosario, CONICET, Fac Ciencias Bioquim & Farmaceut, Area Farmacol, Rosario, Santa Fe, Argentina
关键词
Cisplatin; Acute kidney injury; Caveolin-2; Urinary biomarker; ACUTE KIDNEY INJURY; ORGANIC ANION TRANSPORTER; EXPRESSION; EXCRETION; PROTEIN; SERUM; OAT5; CREATININE; PREDICTION; SEVERITY;
D O I
10.1016/j.toxlet.2019.07.010
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Acute kidney injury (AKI) is a heterogeneous clinical syndrome with diverse outcomes. The recovery from AKI has prognostic importance. Little research has been done in order to find biomarkers that can predict recovery from AKI. Cav-2 is one of the main constituents of caveolae and is expressed in kidney. This study analyzed the time course of Cav-2 urinary excretion and renal expression in rats treated with cisplatin. Male Wistar rats were injected with cisplatin (5 mg/kg b.w., i.p.), and the studies were performed after 2, 4 and 14 days. Cav-2 abundance was evaluated in urine, in renal homogenates and in apical membranes by Western blotting. Cav-2 in urine was increased only 14 days after treatment, in the recovery phase of cisplatin-induced AKI. These results show that Cav-2 in urine could be useful as a biomarker of renal recovery, but not as an early biomarker of cisplatin-induced AKI. Cav-2 expression in total renal homogenates was not modified with treatment, but a down-regulation of Cav-2 in apical membranes was observed in treated animals. We hypothesize that Cav-2 internalizes into renal cells from their apical membrane in response to cisplatin, and regulates in this manner different signaling proteins involved in the physiopathology of renal damage.
引用
收藏
页码:169 / 177
页数:9
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