Summary: Recently, diffusion-weighted magnetic reso nance imaging (DWI) has been shown to visualize acute ischemic lesions in the brain before changes are observ able with conventional magnetic resonance imaging. However, the underlying mechanisms of these acute DWI changes are unclear and may include both reversible and irreversible damage. In this study, we demonstrate that acute DWI lesions may be reversed with MK801 therapy postischemia. Sprague-Dawley rats (n = 12) were sub jected to middle cerebral artery occlusion and DWI scans were obtained beginning 60 min postocclusion. Distinct regions of hyperintensity wgre observed in the basal gan glia and cortex, corresponding with the expected distri bution of ischemia in this model. After the first scan, animals were treated with MK801 (0.5 mg/kg i.v.) or nor-
Magnetic resonance imaging (MRI) has beenshown to be a sensitive method for detecting stroke noninvasively (Matthews et aI. , 1992 Abbreviations used: ANOV A, analysis of variance; DWI, dif fusion-weighted magnetic resonance imaging; MABP, mean ar terial blood pressure; MCAO, middle cerebral artery occlusion; MRI, magnetic resonance imaging; ROI, region of interest; SIR, signal intensity ratio; TlW, Tl-weighted; T2W, T2-weighted.
597mal saline and subsequently scanned again 30 and 60 min after treatment. In the control group, the area of hyper intense lesions continued to increase, by 55% in the cor tex and 57% in the basal ganglia. MK801 therapy signif icantly (p < 0.01) reduced the area of damage by the third DWI scan at 60 min posttreatment ( -50% cortex, -22% basal ganglia, -41% total hemisphere) compared to pre treatment scans. Tetrazolium (TTC) stains at 24 h con firmed that MK801 significantly reduced the volumes of infarction (p < 0.05). These results demonstrate that sig nificant portions of the acute ischemic lesion on DWI are reversible with pharmacologic intervention.