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|Title:||Imaging the ischemic penumbra with 18F-fluoromisonidazole in a rat model of ischemic stroke.||Austin Authors:||Saita, Kazuko;Chen, Michelle;Spratt, Neil J;Porritt, Michelle J;Liberatore, Gabriel T;Read, Stephen J;Levi, Christopher R;Donnan, Geoffrey A ;Ackermann, Uwe ;Tochon-Danguy, Henri J ;Sachinidis, John I;Howells, David William||Affiliation:||Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia toria, Australia||Issue Date:||11-Mar-2004||Publication information:||Stroke; A Journal of Cerebral Circulation 2004; 35(4): 975-80||Abstract:||The ischemic penumbra is a major focus of stroke research. 18F-fluoromisonidazole (18F-FMISO), a positron emission tomography (PET) marker of hypoxic cells, has shown promise as a technique to image the penumbra in humans. Our aim was to delineate the pattern of 18F-FMISO binding in a rat middle cerebral artery transient thread-occlusion model, and correlate this with tissue outcome at 24 hours. We hypothesized that the pattern of 18F-FMISO binding would mimic that seen in humans.Thirty-eight rats underwent 2 hours transient middle cerebral artery (MCA) occlusion, and then received 18F-FMISO at time points from 0.5 to 22 hours post-MCA occlusion and were killed 2 hours later. Autoradiographic assessment of 18F-FMISO binding and assessment (triphenyltetrazolium chloride) of the area of infarction were performed on tissue slices.Until 1 hour after MCA occlusion, 18F-FMISO binding was increased in the entire MCA territory, with little or no infarction visible. Over the next 5 hours, the pattern of binding evolved to a small rim of intensely binding tissue surrounding the infarct core, which itself showed reduced binding compared with the contralateral hemisphere. By 24 hours, there was minimal accumulation of 18F-FMISO binding and a large area of infarction.The pattern of 18F-FMISO binding rats reproduced the pattern seen in humans, consistent with this tracer being a marker of the ischemic penumbra in both species. This technique may have application in studying the ischemic penumbra in animal models, and correlating this with similar studies in humans.||Gov't Doc #:||15017016||URI:||http://ahro.austin.org.au/austinjspui/handle/1/9711||DOI:||10.1161/01.STR.0000121647.01941.ba||URL:||https://pubmed.ncbi.nlm.nih.gov/15017016||Type:||Journal Article||Subjects:||Animals
Brain Ischemia.pathology.radionuclide imaging
Infarction, Middle Cerebral Artery.pathology.radionuclide imaging
Misonidazole.analogs & derivatives.analysis
|Appears in Collections:||Journal articles|
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