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Technical Refinement of a Bilateral Renal Ischemia-Reperfusion Mouse Model for Acute Kidney Injury Research
Published on: November 3, 2023
Renoprotective approaches and strategies in acute kidney injury
Yuan Yang1, Meifang Song1, Yu Liu1
1Department of Nephrology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
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.
Insights
Acute kidney injury (AKI) treatments show promise in preclinical studies by targeting inflammation and cell damage. However, clinical translation remains a challenge, necessitating novel strategies like combination therapy for effective AKI management.
Area of Science:
- Nephrology
- Renal Medicine
- Translational Medicine
Background:
- Acute kidney injury (AKI) is a prevalent renal disease with high mortality rates.
- Numerous chemical, biological, and cell-based therapies have demonstrated potential benefits in preclinical AKI models.
- Current therapeutic strategies aim to mitigate kidney damage by addressing oxidative stress, inflammation, and cell death.
Purpose of the Study:
- To review existing findings on renoprotective agents and therapies for AKI.
- To propose experimental strategies for identifying clinically viable renoprotective methods.
- To advocate for combination therapy approaches targeting multiple pathways in AKI.
Main Methods:
- Comprehensive literature review of preclinical and clinical studies on AKI treatments.
- Analysis of mechanistic pathways targeted by potential renoprotective agents (e.g., oxidative stress, autophagy).
- Evaluation of strategies for translating research findings into clinical practice.
Main Results:
- Despite extensive research, no AKI treatments have been successfully translated into widespread clinical use.
- Various agents and therapies show promise in reducing kidney damage and promoting recovery.
- Mechanisms include mitigating inflammation, oxidative stress, and organellar damage, and activating cytoprotective pathways.
Conclusions:
- There is a critical need for improved strategies to translate promising AKI research into effective clinical treatments.
- Combination therapy, targeting multiple pathways simultaneously, represents a promising avenue for AKI management.
- Further experimental strategies are required to identify and validate renoprotective agents with clinical potential.
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