Spectacular shrinking deficit: insights from multimodal magnetic resonance imaging after embolic middle cerebral artery occlusion in Sprague-Dawley rats
Document Type
Journal ArticlePublication Date
2007-10-01Keywords
AnimalsDiffusion
Infarction, Middle Cerebral
Artery
Magnetic Resonance Imaging
Male
Rats
Rats, Sprague-Dawley
Regional Blood Flow
Software
Neurology
Metadata
Show full item recordAbstract
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), T(1)-(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.Source
J Cereb Blood Flow Metab. 2007 Oct;27(10):1756-63. Epub 2007 Mar 21. Link to article on publisher's siteDOI
10.1038/sj.jcbfm.9600477Permanent Link to this Item
http://hdl.handle.net/20.500.14038/37577PubMed ID
17377514Related Resources
Link to article in PubMedae974a485f413a2113503eed53cd6c53
10.1038/sj.jcbfm.9600477