High Temporal Resolution Diffusion MRI of Global Cerebral Ischemia and Reperfusion

Author:

Pierpaoli Carlo1,Alger Jeffry R.12,Righini Andrea1,Mattiello James3,Dickerson Russell1,Pres Daryl Des4,Barnett Alan1,Chiro Giovanni Di1

Affiliation:

1. Neuroimaging Branch, National Institute of Neurological Diseases and Stroke

2. Department of Radiological Sciences, UCLA, Los Angeles, California, U.S.A.

3. Biomedical Engineering and Instrumentation Program, Bethesda, Maryland

4. In Vivo NMR Center, NCRR, National Institutes of Health, Bethesda, Maryland

Abstract

Although brain ischemia has been extensively studied using diffusion-weighted magnetic resonance imaging, most studies performed so far have not had adequate time resolution to follow the temporal changes in the water apparent diffusion coefficient (ADC) in hyperacute ischemia. Using diffusion echo planar imaging, we obtained ADC maps (calculated from measurements made with 8 b-values) with a time resolution of 43 s in a feline model of global brain ischemia and reperfusion. Different protocols were performed: 10-min hypoperfusion, 10- and 22-min ischemia followed by reperfusion, and cardiac arrest. ADC values were obtained from white matter of the internal capsule and from the thalamus. Cortical gray matter measurements were not deemed reliable due to the close proximity of CSF in the cortical sulci. Following occlusion, the ADC declined in the thalamus to <2 SD of its normal baseline value within 1.5–2.5 min. This decay was exponential with a time constant (τ ± SD) of 6.0 ± 2.6 min; no further decrease in the ADC was observed 10 min following ischemia. Following reperfusion, in animals that showed ADC recovery, the ADC began increasing immediately, returning to its preischemic value in ∼15 min. No significant ADC changes were observed during hypoperfusion. Following cardiac arrest, the decay of ADC was more rapid in the thalamus (τ = 2.6 ± 0.6 min) than in white matter (τ = 6.6 ± 1.8 min). We observed that the ADC at 40 min after cardiac arrest was similar to the ADC at 10 min after ischemia. Given that all animals subjected to 10-min ischemic episodes showed ADC recovery with reperfusion, doubt is cast on whether it is possible to define a threshold value of the ADC below which brain tissue is irreversibly damaged. Finally, despite variability in the time constants of the ADC decay induced by ischemia, the ADC values at 10 min were very similar in all the animals. This suggests that when blood flow is diminished sufficiently to induce an ADC reduction, differences in perfusion affect the rapidity of the decrease but not the final asymptotic value reached.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Clinical Neurology,Neurology

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