Renoprotective approaches and strategies in acute kidney injury

被引:96
作者
Yang, Yuan [1 ]
Song, Meifang [1 ]
Liu, Yu [1 ]
Liu, Hong [1 ]
Sun, Lin [1 ]
Peng, Youming [1 ]
Liu, Fuyou [1 ]
Venkatachalam, Manjeri A. [2 ]
Dong, Zheng [1 ,3 ,4 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Nephrol, Changsha, Hunan, Peoples R China
[2] Univ Texas Hlth Sci Ctr San Antonio, Dept Pathol, San Antonio, TX 78229 USA
[3] Augusta Univ, Dept Cellular Biol & Anat, Med Coll Georgia, Augusta, GA USA
[4] Charlie Norwood VA Med Ctr, 1459 Laney Walker Blvd, Augusta, GA 30912 USA
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
Acute kidney injury; Kidney protection; Kidney repair; Renoprotection; Ischemia-reperfusion; Nephrotoxicity; ISCHEMIA-REPERFUSION INJURY; RENAL ISCHEMIA/REPERFUSION INJURY; MESENCHYMAL STEM-CELLS; MELANOCYTE-STIMULATING HORMONE; ENDOTHELIAL PROGENITOR CELLS; REGULATORY T-CELLS; GROWTH-FACTOR RECEPTOR; MITOCHONDRIAL PERMEABILITY TRANSITION; CISPLATIN-INDUCED NEPHROTOXICITY; NA+/CA2+ EXCHANGE INHIBITOR;
D O I
10.1016/j.pharmthera.2016.03.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Acute kidney injury (AKI) is a major renal disease associated with high mortality rate and increasing prevalence. Decades of research have suggested numerous chemical and biological agents with beneficial effects in AKI. In addition, cell therapy and molecular targeting have been explored for reducing kidney tissue damage and promoting kidney repair or recovery from AKI. Mechanistically, these approaches may mitigate oxidative stress, inflammation, cell death, and mitochondrial and other organellar damage, or activate cytoprotective mechanisms such as autophagy and pro-survival factors. However, none of these findings has been successfully translated into clinical treatment of AKI. In this review, we analyze these findings and propose experimental strategies for the identification of renoprotective agents or methods with clinical potential. Moreover, we propose the consideration of combination therapy by targeting multiple targets in AKI. (C) 2016 Elsevier Inc All rights reserved.
引用
收藏
页码:58 / 73
页数:16
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