| Literature DB >> 27108948 |
Yuan Yang1, Meifang Song1, Yu Liu1, Hong Liu1, Lin Sun1, Youming Peng1, Fuyou Liu2, Manjeri A Venkatachalam3, Zheng Dong4.
Abstract
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.Entities:
Keywords: Acute kidney injury; Ischemia–reperfusion; Kidney protection; Kidney repair; Nephrotoxicity; Renoprotection
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Year: 2016 PMID: 27108948 PMCID: PMC5123830 DOI: 10.1016/j.pharmthera.2016.03.015
Source DB: PubMed Journal: Pharmacol Ther ISSN: 0163-7258 Impact factor: 12.310