The interaction of intra-ischemic and postischemic events in the pathogenesis of ischemic brain injury will be studied in a model of diffuse, high-grade, reversible cerebral hemispheral ischemia in the awake rat. Ischemia will be produced in rats with prior occlusions of the vertebral arteries by bilateral common carotid artery occlusions. This insult produces coma and an isoelectric electroencephalogram in most animals. Removal of the carotid ligatures permits cerebral recirculation. Autoradiographic methods of local cerebral blood flow (14C-iodoantipyrine) and local cerebral glucose utilization (14C-2-deoxyglucose) will be employed. These data will be correlated with regional patterns of ATP and pH alterations and with regional NADH fluorescence, using topographic, pictorial methods. Regional assessments of glycolytic and energy metabolites, indices of free radical reactions, brain water and ion homeostasis, blood-brain barrier function, and histopathological alterations will be performed. The effects of preischemic glucose administration and of postischemic hypertension and hyperoxygenation on the severity of ischemic injury will be assessed. These studies will define regionally heterogeneous patterns of ischemic brain injury and will serve to clarify the contributions of events during ischemia and of postischemic factors in producing these lesions. The results will provide data on the basis of which future studies of the efficacy of therapeutic agents in ameliorating brain ischemia may be carried out.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS005820-24
Application #
3099245
Study Section
(SRC)
Project Start
1976-08-01
Project End
1990-07-31
Budget Start
1989-08-01
Budget End
1990-07-31
Support Year
24
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Miami School of Medicine
Department
Type
Schools of Medicine
DUNS #
City
Miami
State
FL
Country
United States
Zip Code
33101
Dave, Kunjan R; Della-Morte, David; Saul, Isabel et al. (2013) Ventricular fibrillation-induced cardiac arrest in the rat as a model of global cerebral ischemia. Transl Stroke Res 4:571-8
Della-Morte, D; Raval, A P; Dave, K R et al. (2011) Post-ischemic activation of protein kinase C ? protects the hippocampus from cerebral ischemic injury via alterations in cerebral blood flow. Neurosci Lett 487:158-62
Dave, Kunjan R; Anthony Defazio, Richard; Raval, Ami P et al. (2009) Protein kinase C epsilon activation delays neuronal depolarization during cardiac arrest in the euthermic arctic ground squirrel. J Neurochem 110:1170-9
DeFazio, R Anthony; Raval, Ami P; Lin, Hung W et al. (2009) GABA synapses mediate neuroprotection after ischemic and epsilonPKC preconditioning in rat hippocampal slice cultures. J Cereb Blood Flow Metab 29:375-84
Della-Morte, D; Dave, K R; DeFazio, R A et al. (2009) Resveratrol pretreatment protects rat brain from cerebral ischemic damage via a sirtuin 1-uncoupling protein 2 pathway. Neuroscience 159:993-1002
Park, Hee-Pyoung; Nimmagadda, Anitha; DeFazio, Richard A et al. (2008) Albumin therapy augments the effect of thrombolysis on local vascular dynamics in a rat model of arteriolar thrombosis: a two-photon laser-scanning microscopy study. Stroke 39:1556-62
Dave, Kunjan R; DeFazio, R Anthony; Raval, Ami P et al. (2008) Ischemic preconditioning targets the respiration of synaptic mitochondria via protein kinase C epsilon. J Neurosci 28:4172-82
Kim, Eun J; Raval, Ami P; Perez-Pinzon, Miguel A (2008) Preconditioning mediated by sublethal oxygen-glucose deprivation-induced cyclooxygenase-2 expression via the signal transducers and activators of transcription 3 phosphorylation. J Cereb Blood Flow Metab 28:1329-40
Nimmagadda, Anitha; Park, Hee-Pyoung; Prado, Ricardo et al. (2008) Albumin therapy improves local vascular dynamics in a rat model of primary microvascular thrombosis: a two-photon laser-scanning microscopy study. Stroke 39:198-204
Kim, E; Raval, A P; Defazio, R A et al. (2007) Ischemic preconditioning via epsilon protein kinase C activation requires cyclooxygenase-2 activation in vitro. Neuroscience 145:931-41

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