Spectacular shrinking deficit: insights from multimodal magnetic resonance imaging after embolic middle cerebral artery occlusion in Sprague-Dawley rats

被引:9
作者
Henninger, Nils
Sicard, Kenneth M.
Fisher, Marc
机构
[1] Univ Massachusetts, Sch Med, Dept Psychiat, Ctr Comparat NeuroImaging, Worcester, MA 01604 USA
[2] Univ Massachusetts, Sch Med, Dept Neurol, Worcester, MA 01604 USA
关键词
diffusion weighted imaging; focal cerebral ischemia; functional magnetic resonance imaging; ischemic penumbra; perfusion weighted imaging; transient ischemic attack;
D O I
10.1038/sj.jcbfm.9600477
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Almost no data is available on the serial changes in the brain after spectacular shrinking deficit (SSD) that may help understand this relatively rare clinical phenomenon. Quantitative diffusion(DWI),perfusion-(PWI), T1-(T1WI), T-2-weighted ( T2WI), and functional magnetic resonance imaging ( fMRI) were performed before, during, and up to 7 days after embolic middle cerebral artery occlusion ( eMCAO) in male Sprague-Dawley rats ( n = 9). Region of interest (ROI) analysis was used to evaluate structural and functional MR signal changes within three ROIs defined by the apparent diffusion coefficient ( ADC), cerebral blood flow ( CBF) signatures, and final tissue viability. DWI, PWI, and T2WI lesion volumes were calculated using previously established viability thresholds and final infarct volumes ascertained with 2,3,5-triphenyltetrazolium chloride (TTC) staining. Serial MRI demonstrated spontaneous reperfusion of initially hypoperfused MCA regions accompanied by substantial reduction of initial ADC and CBF lesions and gradual recovery of neurological outcome. Recovery rates of CBF/ADC abnormalities differed among ROIs. Functional magnetic resonance imaging showed persistent tissue dysfunction after the recovery of the CBF/ADC lesions. This study may facilitate our understanding of the pathophysiological mechanisms by which early, spontaneous reperfusion affects tissue fate and neurological function.
引用
收藏
页码:1756 / 1763
页数:8
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