Quantitative cerebrovascular reactivity MRI in mice using acetazolamide challenge
Zhiliang Wei1,2, Yuguo Li1,2, Xirui Hou3
1Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Magnetic Resonance in Medicine
|June 17, 2022
Summary
This study introduces a new quantitative MRI method to measure cerebrovascular reactivity (CVR) in mice using acetazolamide. The technique successfully mapped regional CVR differences, proving its feasibility for preclinical research.
Area of Science:
- Neuroimaging
- Cerebrovascular Research
- Preclinical MRI
Background:
- Cerebrovascular reactivity (CVR) assessment is crucial for understanding brain health.
- Current CVR methods in mice have limitations.
- Developing quantitative MRI techniques is essential for preclinical research.
Purpose of the Study:
- To develop and validate a quantitative MRI method for estimating cerebrovascular reactivity (CVR) in mice.
- To assess the cerebral vasodilatory response to acetazolamide (ACZ) using MRI.
- To establish a reliable method for regional CVR mapping in rodent models.
Main Methods:
- Utilized phase-contrast or pseudo-continuous arterial spin labeling MRI to measure cerebral blood flow (CBF).
- Determined vasodilatory input intensity via plasma ACZ levels measured by high-performance liquid chromatography.
- Investigated dose dependence and regional CVR variations, comparing ACZ injections to control experiments.
Main Results:
- CBF showed an exponential increase post-ACZ injection (time constant: 1.62 min).
- Plasma ACZ concentration increased linearly with dose (30-180 mg/kg), but CBF changes were not dose-dependent.
- Regional CVR analysis revealed higher reactivity in the isocortex compared to deep-brain regions.
Conclusions:
- Demonstrated the proof-of-principle for a novel quantitative CVR mapping technique in mice.
- The developed MRI method is feasible for preclinical cerebrovascular research.
- This technique allows for regional CVR assessment in rodent models.


