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Long‐term measurement of cerebral blood flow and metabolism in a rat chronic hypoperfusion model
148
Citations
31
References
2003
Year
White MatterSocial SciencesCerebral Vascular RegulationNeurovascular DiseaseBlood FlowAppropriate ModelStrokeOccipital CortexBrain InjuryNeurologyLong‐term MeasurementNeuropathologyBlood Flow MeasurementIschemic SyndromeChronic Cerebral HypoperfusionVascular BiologyCerebral Blood FlowNervous SystemReperfusion InjuryNeurophysiologyNeuroanatomyPhysiologyTissue OxygenationNeuroscienceMetabolismMedicine
1. Rat bilateral common carotid artery occlusion (BCAO) was used as a chronic cerebral hypoperfusion model. We observed autoradiographically the long-term changes in regional cerebral blood flow (rCBF) and regional cerebral glucose utilization (rCGU) after 2 days and 1, 4 and 8 weeks of BCAO and in controls. Regions evaluated included the cerebral cortex, white matter and basal ganglia. Pathological changes were also observed with Klüver-Barrera and haematoxylin-eosin staining. 2. After 2 days, rCBF was significantly reduced to 33-58% in the cortex, white matter and amygdala and similar reductions were observed after 1 week. 3. After 4 weeks, rCBF recovered; however, rCBF remained significantly reduced in the occipital cortex, white matter, globus pallidus and substantia nigra. 4. After 2 days, rCGU was mostly maintained but, after 1 week, rCGU was reduced significantly to 40-70% in the cortex, white matter, basal ganglia and thalamus. Four weeks later, these reductions were no longer seen. 5. Rarefaction of the white matter was observed from 1 week. 6. These results showed that the BCAO in rats is an appropriate model for chronic cerebral hypoperfusion and that uncoupling of rCBF and rCGU was observed from 2 days until 4 weeks in the white matter.
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