YM872, a highly water-soluble AMPA receptor antagonist, preserves the hemodynamic penumbra and reduces brain injury after permanent focal ischemia in rats.

BACKGROUND AND PURPOSE We recently described an image analysis technique based on the temporal correlation mapping (TCM) of injected contrast agents that can be used to distinguish the hemodynamic core and hemodynamic penumbra after focal ischemia. In this study we used this technique for the first time to investigate the effects of the water-soluble AMPA receptor antagonist YM872 in permanent focal ischemia. METHODS Fischer 344 rats were subjected to permanent occlusion of the middle cerebral artery. Approximately 30 minutes after ischemia, functional CT images were collected with the use of a dynamic scanning protocol with bolus injections of nonionic contrast agent iohexol (1 mL/kg). TCM analysis defined the distributions of hemodynamic core and hemodynamic penumbra. Cerebral perfusion indices were calculated on the basis of the area under the first-pass transit curves. One hour after ischemia, animals were randomly treated with YM872 (n=8, 20 mg/kg per hour over 4 hours) or normal saline (n=10). Twenty-four hours later, neurological deficits were evaluated, and conventional CT and triphenyltetrazolium chloride staining were used to define volumes of ischemic damage. RESULTS At 24 hours after ischemia, hypodense lesions were visible on conventional CT scans that were highly correlated with triphenyltetrazolium chloride lesion volumes. YM872 improved neurological deficits and reduced volumes of ischemic damage in cortex (90+/-14 versus 170+/-16 mm3 in controls) but not striatum (57+/-14 versus 79+/-6 mm3 in controls). Comparison of early TCM images with conventional CT scans of ischemic injury showed that the hemodynamic core was always damaged in all rats. In controls, 54% of the tissue within the hemodynamic penumbra evolved into ischemic damage compared with 24% in YM872-treated rats. Furthermore, the perfusion index corresponding to the ischemic damage threshold was significantly reduced by YM872 (28+/-2% versus 37+/-2% in controls). CONCLUSIONS These results indicate that YM872 is a neuroprotective compound that ameliorates the deterioration of the hemodynamic penumbra after focal ischemia.

[1]  H. Kamiya,et al.  Glutamate receptors in the mammalian central nervous system , 1998, Progress in Neurobiology.

[2]  B. Siesjö,et al.  Calcium in ischemic cell death. , 1998, Stroke.

[3]  M D Ginsberg,et al.  Transient Middle Cerebral Artery Occlusion by Intraluminal Suture: II. Neurological Deficits, and Pixel-Based Correlation of Histopathology with Local Blood Flow and Glucose Utilization , 1997, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[4]  J. Connor,et al.  Global Ischemia Induces Downregulation of Glur2 mRNA and Increases AMPA Receptor-Mediated Ca2+ Influx in Hippocampal CA1 Neurons of Gerbil , 1997, The Journal of Neuroscience.

[5]  R. Storb,et al.  Glucocorticoids fail to enhance the effect of FK506 and methotrexate in prevention of graft-versus-host disease after DLA-nonidentical, unrelated marrow transplantation , 1997, Bone Marrow Transplantation.

[6]  J. Mandeville,et al.  Neuroprotection with NBQX in rat focal cerebral ischemia. Effects on ADC probability distribution functions and diffusion-perfusion relationships. , 1997, Stroke.

[7]  R. Gonzalez,et al.  MRI Measurements of Water Diffusion and Cerebral Perfusion: Their Relationship in a Rat Model of Focal Cerebral Ischemia , 1997, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[8]  B. Rosen,et al.  High resolution measurement of cerebral blood flow using intravascular tracer bolus passages. Part II: Experimental comparison and preliminary results , 1996, Magnetic resonance in medicine.

[9]  G L Wolf,et al.  Measurement of cerebral blood volume with subtraction three-dimensional functional CT. , 1996, AJNR. American journal of neuroradiology.

[10]  B. Rosen,et al.  High resolution measurement of cerebral blood flow using intravascular tracer bolus passages. Part I: Mathematical approach and statistical analysis , 1996, Magnetic resonance in medicine.

[11]  M. Moskowitz,et al.  Temporal correlation mapping analysis of the hemodynamic penumbra in mutant mice deficient in endothelial nitric oxide synthase gene expression. , 1996, Stroke.

[12]  E. Lo,et al.  Hemodynamic alterations in focal cerebral ischemia: temporal correlation analysis for functional imaging. , 1996, Neurological research.

[13]  G. Gazelle,et al.  Quantitative high-resolution measurement of cerebrovascular physiology with slip-ring CT. , 1996, AJNR. American journal of neuroradiology.

[14]  K.,et al.  Temporal Correlation Analysis of Penumbral Dynamics in Focal Cerebral Ischemia , 2010 .

[15]  Kiyoshi Takagi,et al.  Local hemodynamic changes during transient middle cerebral artery occlusion and recirculation in the rat: a [14C]iodoantipyrine autoradiographic study , 1995, Brain Research.

[16]  J. LaManna,et al.  Local Cerebral Glucose Utilization and Cytoskeletal Proteolysis as Indices of Evolving Focal Ischemic Injury in Core and Penumbra , 1995, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[17]  T. Ng,et al.  Sensitivity of magnetic resonance diffusion-weighted imaging and regional relationship between the apparent diffusion coefficient and cerebral blood flow in rat focal cerebral ischemia. , 1995, Stroke.

[18]  J. Garcìa,et al.  Neuronal necrosis after middle cerebral artery occlusion in Wistar rats progresses at different time intervals in the caudoputamen and the cortex. , 1995, Stroke.

[19]  F. Godtliebsen,et al.  Combined perfusion and diffusion-weighted magnetic resonance imaging in a rat model of reversible middle cerebral artery occlusion. , 1995, Stroke.

[20]  W. J. Lorenz,et al.  Quantification of regional cerebral blood flow and volume with dynamic susceptibility contrast-enhanced MR imaging. , 1994, Radiology.

[21]  D. Graham,et al.  Neuroprotective Effect of the AMPA Receptor Antagonist LY-293558 in Focal Cerebral Ischemia in the Cat , 1994, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[22]  M. Moskowitz,et al.  Nitric Oxide Synthase Inhibition and Cerebrovascular Regulation , 1994, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[23]  A. Buchan,et al.  Delayed Treatment with AMPA, but Not NMDA, Antagonists Reduces Neocortical Infarction , 1994, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[24]  M E Moseley,et al.  High-Speed MR Imaging of Ischemic Brain Injury following Stenosis of the Middle Cerebral Artery , 1993, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[25]  B. Rosen,et al.  Pitfalls in MR measurement of tissue blood flow with intravascular tracers: Which mean transit time? , 1993, Magnetic resonance in medicine.

[26]  A. Hakim,et al.  Time Course of Cerebral Blood Flow and Histological Outcome After Focal Cerebral Ischemia in Rats , 1992, Stroke.

[27]  D. Lodge,et al.  The neuroprotective actions of 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo(F)quinoxaline (NBQX) in a rat focal ischaemia model , 1992, Brain Research.

[28]  B. Siesjö,et al.  Penumbral Tissues Salvaged by Reperfusion Following Middle Cerebral Artery Occlusion in Rats , 1992, Stroke.

[29]  D. J. Cole,et al.  Time- and Pressure-Dependent Changes in Blood–Brain Barrier Permeability After Temporary Middle Cerebral Artery Occlusion in Rats , 1990 .

[30]  E. Nielsen,et al.  2,3-Dihydroxy-6-nitro-7-sulfamoyl-benzo(F)quinoxaline: a neuroprotectant for cerebral ischemia. , 1990, Science.

[31]  L. Pitts,et al.  Rat middle cerebral artery occlusion: evaluation of the model and development of a neurologic examination. , 1986, Stroke.

[32]  D. Graham,et al.  Focal Cerebral Ischaemia in the Rat: 2. Regional Cerebral Blood Flow Determined by [14C]Iodoantipyrine Autoradiography following Middle Cerebral Artery Occlusion , 1981, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[33]  D. Graham,et al.  Focal Cerebral Ischaemia in the Rat: 1. Description of Technique and Early Neuropathological Consequences following Middle Cerebral Artery Occlusion , 1981, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[34]  D. Choi The Excitotoxic Concept , 1997 .

[35]  K. Welch Primer on cerebrovascular diseases , 1997 .

[36]  Joakim Bjorkdahl Very delayed infarction after mild focal cerebral ischemia: A role for apoptosis? , 1996 .

[37]  S. Usuda,et al.  YM90K: pharmacological characterization as a selective and potent alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate/kainate receptor antagonist. , 1996, The Journal of pharmacology and experimental therapeutics.

[38]  Kendall Preston,et al.  Applications of similarity mapping in dynamic MRI , 1995, IEEE Trans. Medical Imaging.

[39]  E. Lo,et al.  Blood-brain barrier disruption in experimental focal ischemia: comparison between in vivo MRI and immunocytochemistry. , 1994, Magnetic resonance imaging.

[40]  Dawson Da Nitric oxide and focal cerebral ischemia: multiplicity of actions and diverse outcome. , 1994 .

[41]  R. Gill The pharmacology of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA)/kainate antagonists and their role in cerebral ischaemia. , 1994, Cerebrovascular and brain metabolism reviews.

[42]  K. Takakura,et al.  Ischemic brain edema following occlusion of the middle cerebral artery in the rat. I: The time courses of the brain water, sodium and potassium contents and blood-brain barrier permeability to 125I-albumin. , 1985, Stroke.