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In vivo cerebrovascular reactivity in Wistar and Fischer 344 rat strains during aging
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1993
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AgingBiogerontologyFischer 344Oxidative StressCerebral Vascular RegulationLongevityIntracranial PressureBrain InjuryNeurologyAtherosclerosisHealth SciencesHypoxia (Medicine)Vascular BiologyCerebral Blood FlowVivo Cerebrovascular ReactivityCbf RegulationNeurophysiologyNeuroanatomyPhysiologyRat StrainsBasal CbfCellular SenescenceNeuroscienceCentral Nervous SystemMedicineVascular Aging
Basal cerebral blood flow (CBF) and CBF regulation after hypercapnia and hypotensive hemorrhage were investigated using H2 clearance in the frontal cortex of awake 2-, 14-, or 23-mo-old Wistar or Fischer 344 rats. Basal CBF decreased in old Wistar but not in mature Wistar (old 64.4 +/- 2.8, mature 87.6 +/- 2.6, young 79.6 +/- 2.2 ml.min-1 x 100 g-1) or in old Fischer 344 (old 71.9 +/- 2.9, young 73.3 +/- 1.6 ml.min-1 x 100 g-1) rats. Cerebrovascular reactivity to hypercapnia decreased in mature and old Wistar (old 2.1 +/- 0.3, mature 3.1 +/- 0.7, young 7.0 +/- 2.1 ml.min-1 x 100 g-1 x mmHg-1) but not in old Fischer 344 rats (old 4.6 +/- 1.4, young 4.9 +/- 0.9 ml.min-1 x 100 g-1 x mmHg-1). The lower limit of CBF autoregulation increased by 20 mmHg during maturation and/or aging in the two strains. Because blood gases and pH evolved similarly in both strains, we postulate that differences in cerebrovascular structure and/or function explain the differences in CBF regulation in the older representatives of the two strains.