TY - JOUR
T1 - Renoprotective approaches and strategies in acute kidney injury
AU - Yang, Yuan
AU - Song, Meifang
AU - Liu, Yu
AU - Liu, Hong
AU - Sun, Lin
AU - Peng, Youming
AU - Liu, Fuyou
AU - Venkatachalam, Manjeri A.
AU - Dong, Zheng
N1 - Funding Information:
This study was supported in part by grants from the National Natural Science Foundation of China ( 81430017 ), the Hunan Province Natural Science Foundation, China ( no.2009TP-1066-2 ), the National Basic Research Program of China 973 , program no. 2012CB517601 , the scientific research project of the Hunan Province Education Department ( 14C0911 ), and the National Institutes of Health and Department of Veterans Administration of USA .
Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/7/1
Y1 - 2016/7/1
N2 - 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.
AB - 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.
KW - Acute kidney injury
KW - Ischemia-reperfusion
KW - Kidney protection
KW - Kidney repair
KW - Nephrotoxicity
KW - Renoprotection
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U2 - 10.1016/j.pharmthera.2016.03.015
DO - 10.1016/j.pharmthera.2016.03.015
M3 - Review article
C2 - 27108948
AN - SCOPUS:84971273422
SN - 0163-7258
VL - 163
SP - 58
EP - 73
JO - Pharmacology and Therapeutics, Part A: Chemotherapy, Toxicology and
JF - Pharmacology and Therapeutics, Part A: Chemotherapy, Toxicology and
ER -