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Updated: Jul 1, 2026

Use of Ultra-high Field MRI in Small Rodent Models of Polycystic Kidney Disease for In Vivo Phenotyping and Drug Monitoring
Published on: June 23, 2015
Comparative ex vivo 7T MRI study of renal microstructural changes in cats with and without chronic kidney disease
Takumi Matsuura1, Hiroshi Satoh2, Masaaki Katayama3
1Toray Industries, Inc., Tokyo, Japan.
Background:
Seven-tesla magnetic resonance imaging (7T MRI) noninvasively detects microstructural changes associated with chronic kidney disease (CKD). Using animal-specific coils is often necessary to obtain high resolution and to minimize artifacts from breathing and heartbeat, even under anesthesia. However, in feline medicine, this ultra-high-field imaging has not been investigated either in vivo or even ex vivo using explanted organs.
Aim:
This study aimed to use a high-resolution ex vivo imaging approach to characterize microstructural changes in a kidney from a cat with CKD compared to a background-matched control, and to correlate the magnetic resonance imaging (MRI) findings with histopathology, focusing on the relationship between the apparent diffusion coefficient (ADC) and interstitial fibrosis.
Methods:
We imaged the postmortem kidneys of a cat with the International Renal Interest Society Stage 2 CKD and a background-matched control using a 7T MRI system. High-resolution T2-weighted imaging and diffusion-weighted imaging (DWI) sequences were acquired to generate ADC maps. We measured mean ADC values in the cortex and medulla and correlated these values with the degree of interstitial fibrosis, assessed by Masson's trichrome staining.
Results:
On T2-weighted images, the CKD kidney showed a loss of corticomedullary differentiation, whereas the control kidney maintained a clear definition. The mean ADC value in the renal cortex of the CKD cat (432 ± 8 μm²/sec) was lower than that in the non-chronic kidney disease cat (609 ± 15 μm²/sec). A lower ADC value was also found in the outer medulla of the CKD kidney. In contrast, the ADC value in the inner medulla was higher in the CKD kidney (1,088 ± 19 μm²/sec) compared to the control (962 ± 26 μm²/sec). Histopathology confirmed extensive interstitial fibrosis in the CKD kidney, but only minimal fibrosis in the control kidney.
Conclusion:
High-resolution ex vivo MRI can detect microstructural changes in the feline CKD kidney. In particular, we found that a decreased cortical ADC value is strongly associated with interstitial fibrosis. These findings suggest that DWI could be a promising noninvasive tool for assessing the pathology of feline CKD and provide a basis for future studies in living animals.
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