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Updated: May 12, 2026

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Quantitative mouse renal perfusion using arterial spin labeling.

Reshmi Rajendran1, Si Kang Lew, Cai Xian Yong

  • 1Magnetic Resonance Imaging Group, Singapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.

NMR in Biomedicine
|April 18, 2013
PubMed
Summary
This summary is machine-generated.

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Arterial spin labeling MRI successfully quantified mouse renal perfusion, overcoming previous challenges. This noninvasive technique shows promise for studying kidney function and disease models.

Area of Science:

  • Biomedical Imaging
  • Renal Physiology
  • Magnetic Resonance Imaging

Background:

  • Accurate renal perfusion information is crucial for diagnosing and prognosing kidney function.
  • Gadolinium-based contrast agents have limitations for renal perfusion quantification due to glomerular filtration and safety concerns in patients with kidney dysfunction.
  • Arterial spin labeling (ASL) MRI offers a noninvasive method for perfusion quantification but faces challenges in mouse models due to low sensitivity and artifacts.

Purpose of the Study:

  • To investigate the feasibility and application of ASL MRI for quantifying renal perfusion in mice.
  • To optimize ASL MRI parameters for high-quality mouse renal perfusion imaging.
  • To assess the impact of oxygen and carbogen breathing on mouse renal perfusion and T1 values.

Main Methods:

Keywords:
MRIarterial spin labelingcarbogenflow-sensitive alternating inversion recovery (FAIR)kidney perfusiontranslational

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The Mouse Isolated Perfused Kidney Technique
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  • Mouse renal perfusion was studied using flow-sensitive alternating inversion recovery (FAIR) ASL MRI at 7 Tesla.
  • Respiratory, susceptibility, and fat artifacts were controlled using triggering, high-order shimming, and water excitation, respectively, with spin-echo echo-planar imaging.
  • Perfusion measurements were compared between 100% oxygen and carbogen (95% O2/5% CO2) breathing conditions.

Main Results:

  • High-quality renal perfusion images were obtained in mice.
  • Renal cortical perfusion was significantly higher than medullary perfusion.
  • Cortical perfusion increased from 397 ± 36 to 476 ± 73 mL/100g/min under carbogen.
  • Medullary perfusion increased from 166 ± 41 to 203 ± 40 mL/100g/min under carbogen.
  • T1 relaxation times decreased in both cortex and medulla under carbogen compared to 100% oxygen.

Conclusions:

  • ASL MRI, particularly with FAIR technique at 7T, is a viable noninvasive method for quantifying mouse renal perfusion.
  • The study demonstrated significant differences in cortical and medullary perfusion and their responses to gas challenges.
  • This technique holds potential for advancing research in mouse models of renal diseases.