Renalase contributes to protection against renal fibrosis via inhibiting oxidative stress in rats

• Published in: International urology and nephrology Vol. 50; no. 7; pp. 1347 - 1354
• Main Authors: Wu, Yiru, Wang, Liyan, Wang, Xiaoqi, Wang, Yahui, Zhang, Qidong, Liu, Wenhu
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Netherlands 01.07.2018; Springer Nature B.V
• Subjects: Animals; Biomarkers - blood; Cells, Cultured; Disease Models, Animal; End-stage renal disease; Fibrosis; Fibrosis - prevention & control; Humans; Kidney diseases; Kidney Tubules, Proximal - metabolism; Male; Medicine; Medicine & Public Health; Mesenchyme; Monoamine Oxidase - metabolism; Nephrology; Nephrology - Original Paper; Oxidation; Oxidative stress; Oxidative Stress - drug effects; Random Allocation; Rats; Rats, Sprague-Dawley; Renal Insufficiency, Chronic - metabolism; Renal Insufficiency, Chronic - pathology; Renal Insufficiency, Chronic - physiopathology; Rodents; Role; Sensitivity and Specificity; Supplements; Urology; Oxidative stress; Renalase; Renal interstitial fibrosis; Epithelial–mesenchymal transition; Chronic kidney disease
• ISSN: 0301-1623; 1573-2584
• DOI: 10.1007/s11255-018-1820-2

Background Renal interstitial fibrosis (RIF) is a common pathway for progression of chronic kidney disease (CKD) to end-stage renal disease. In our previous study, it has been provided that renalase can ameliorate renal interstitial fibrosis in unilateral ureteral obstruction (UUO) rats. The other mechanism of renalase to alleviate renal fibrosis should be explored. Materials and methods In this study, we evaluated the role of oxidative stress in UUO rats and epithelial–mesenchymal transition (EMT) in human proximal renal tubular epithelial (HK-2) cells and examined the association of renalase. Results Oxidative stress could induce EMT and fibrosis in HK-2 cells. In the UUO model, oxidative stress occurred and maintained at a high level leading to RIF. Administration of renalase by adenovirus significantly attenuated oxidative stress and further in vitro study showed that renalase can exert anti-fibrosis by inhibiting oxidative stress. Conclusion Our results prompt another mechanism of anti-fibrotic renal protection of renalase, which may be partly associated with inhibiting oxidative stress. These data provided another theoretical basis that supplementation with exogenous renalase may be a promising strategy for slowing or halting the progression of CKD.