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3 min read

Acute Kidney Injury: Insights From In Vivo Biomarker Assessments

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In vivo Acute Kidney Injury (AKI) models are commonly used to study renal damage and evaluating potential therapeutic interventions. Various models are used to simulate AKI, including bilateral occlusion, unilateral occlusion, and nephrectomy combined with unilateral occlusion. In these models, blood is analyzed for biomarkers such as creatinine, BUN, KIM-1, and NGAL, which indicate kidney function and injury severity. Urine is tested for total protein and albumin to assess renal filtration and damage. While rodent models are commonly used, we have also developed a pig model, leveraging the physiological similarities between pigs and humans in organ function and drug response. The comparable kidney size and function of pigs enhance the model’s relevance for studying renal dysfunction and testing potential therapies.

 

Rodent Models of AKI

 

Bilateral Ischemia/Reperfusion Induced AKI in Mice

Blood Creatinine Level 
10 
Naive NO 
swge,• 
Sham 
ocdusim 
(24h) 
(48h) 
Bilateral 
ocdusim 
(48h)

Figure 1. Blood creatinine levels in bilateral ischemia/reperfusion induced AKI in mice indicate a significant increase in blood creatinine levels following bilateral occlusion, demonstrating impaired kidney function.

 

Nephrectomy Followed by Unilateral Occlusion AKI in Rats

Figure 2: Serum biomarkers following nephrectomy and unilateral occlusion model shows a marked increase in serum urea post-occlusion, highlighting progressive kidney impairment.

 

Bilateral Occlusion-Induced AKI in Rats

Figure 3: Serum biomarkers in bilateral occlusion in rats in 25-minute versus 45-minute occlusion show a sharp increase in KIM-1 levels, with more pronounced effects observed in the 45-minute occlusion group, indicating more severe kidney injury.

 

Nephrectomy and Unilateral Occlusion Induced AKI in Pigs

Blood Creatinine (mg/dL) 
•E 08 
02 
Study hours Blood Urea (mg/dL) 
40 
Study hours

Figures 4-5:  Blood creatinine and urea concentrations following AKI increase over time indicating declining kidney function post-injury.

 

The use of various in vivo AKI models, including rodent and pig models, provides valuable insights into the mechanisms of kidney injury and allows for the evaluation of potential therapeutic interventions. Blood biomarkers along with urine analysis are critical tools in assessing renal function and injury severity. While rodent models remain widely used due to their ease of handling and lower cost, the pig model offers an enhanced level of relevance due to its physiological similarities with humans.

 

Learn more about our acute kidney injury models by downloading our datasheet here.

 


 

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