Stroke penumbra defined by an MRI-based oxygen challenge technique: 1. Validation using 14C2-deoxyglucose autoradiography

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Abstract

Accurate identification of ischemic penumbra will improve stroke patient selection for reperfusion therapies and clinical trials. Current magnetic resonance imaging (MRI) techniques have limitations and lack validation. Oxygen challenge T*2 MRI (T*2 OC) uses oxygen as a biotracer to detect tissue metabolism, with penumbra displaying the greatest T*2 signal change during OC. 14 C2-deoxyglucose (2-DG) autoradiography was combined with T *2 OC to determine metabolic status of T *2-defined penumbra. Permanent middle cerebral artery occlusion was induced in anesthetized male Sprague-Dawley rats (n6). Ischemic injury and perfusion deficit were determined by diffusion-and perfusion-weighted imaging, respectively. At 14732 minutes after stroke, T *2 signal change was measured during a 5-minute 100% OC, immediately followed by 125 Ci/kg2-DG, intravenously. Magnetic resonance images were coregistered with the corresponding autoradiograms. Regions of interest were located within ischemic core, T*2-defined penumbra, equivalent contralateral structures, and a region of hyperglycolysis. A T*2 signal increase of 9.22%3.9% (means.d.) was recorded in presumed penumbra, which displayed local cerebral glucose utilization values equivalent to contralateral cortex. T *2 signal change was negligible in ischemic core, 3.2%0.78% in contralateral regions, and 1.41%0.62% in hyperglycolytic tissue, located outside OC-defined penumbra and within the diffusion abnormality. The results support the utility of OC-MRI to detect viable penumbral tissue following stroke. © 2011 ISCBFM All rights reserved.

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Robertson, C. A., McCabe, C., Gallagher, L., Lopez-Gonzalez, M. D. R., Holmes, W. M., Condon, B., … MacRae, I. M. (2011). Stroke penumbra defined by an MRI-based oxygen challenge technique: 1. Validation using 14C2-deoxyglucose autoradiography. Journal of Cerebral Blood Flow and Metabolism, 31(8), 1778–1787. https://doi.org/10.1038/jcbfm.2011.66

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