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Updated: Jun 22, 2025

Standardized Colon Ascendens Stent Peritonitis in Rats - a Simple, Feasible Animal Model to Induce Septic Acute Kidney Injury
Published on: February 15, 2022
Models of sepsis-induced acute kidney injury
Liang Dong1, Yi-Ling Xie1, Ren-Tao Zhang1
1Department of Critical Care Medicine, Taizhou Central Hospital (Taizhou University Hospital), School of Medicine, Taizhou University, Taizhou 318000, Zhejiang, China.
Abstract:
Sepsis-induced acute kidney injury (S-AKI) is one of the most serious life-threatening complications of sepsis. The pathogenesis of S-AKI is complex and there is no effective specific treatment. Therefore, it is crucial to choose suitable preclinical models that are highly similar to human S-AKI to study the pathogenesis and drug treatment. In this review, we summarized recent advances in the development models of S-AKI, providing reference for the reasonable selection of experimental models as basic research and drug development of S-AKI.
Insights
Sepsis-induced acute kidney injury (S-AKI) lacks effective treatments due to complex causes. This review examines preclinical S-AKI models to aid research and drug development for this critical condition.
Area of Science:
- Nephrology
- Critical Care Medicine
- Translational Medicine
Background:
- Sepsis-induced acute kidney injury (S-AKI) is a severe complication of sepsis.
- The complex pathogenesis of S-AKI currently lacks specific effective treatments.
- Developing reliable preclinical models is essential for understanding S-AKI and advancing therapies.
Purpose of the Study:
- To review recent advancements in the development of S-AKI preclinical models.
- To provide guidance for selecting appropriate experimental models for S-AKI research.
- To support basic research and drug development efforts for S-AKI.
Main Methods:
- Literature review of recent studies on S-AKI model development.
- Analysis and synthesis of findings related to various S-AKI models.
- Comparative assessment of model suitability for different research objectives.
Main Results:
- Identified diverse preclinical models for S-AKI, each with unique advantages and limitations.
- Highlighted the importance of model selection based on research questions (pathogenesis vs. drug efficacy).
- Summarized key features and applications of current S-AKI models.
Conclusions:
- Appropriate selection of preclinical models is critical for advancing S-AKI research and therapeutic development.
- Further refinement of S-AKI models is needed to better mimic human disease.
- This review serves as a reference for researchers in the field of S-AKI.
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