Stroke, Vol 19, 245-250, Copyright © 1988 by American Heart Association
RC Vannucci, DT Lyons and F Vasta
Immature rats subjected to a combination of unilateral common carotid
artery ligation and hypoxia sustain brain damage confined largely to the
ipsilateral cerebral hemisphere. To ascertain the extent and distribution
of ischemic alterations in the brains of these small animals, we modified
the Sakurada technique to measure regional cerebral blood flow using
carbon-14 autoradiography. Seven-day-old rats underwent right common
carotid artery ligation following which they were rendered hypoxic with 8%
O2 at 37 degrees C. Before and during hypoxia, the rat pups received an
injection of iodo[14C]antipyrine for determination of regional cerebral
blood flow. Blood flows to individual structures of the ipsilateral
cerebral hemisphere were not influenced by arterial occlusion alone; flows
to the contralateral hemisphere and to the brainstem and cerebellum
actually increased by 25- 50%. Hypoxia-ischemia was associated with
decreases in regional cerebral blood flow of the ipsilateral hemisphere
such that by 2 hours, flows to subcortical white matter, neocortex,
striatum, and thalamus were 15, 17, 34, and 41% of control, respectively.
The hierarchy of the blood flow reductions correlated closely with the
distribution and extent of ischemic neuronal necrosis. However, unlike the
pathologic pattern of this model, the degree of ischemia appeared
homogeneous within each brain region. Blood flows to contralateral cerebral
hemispheric structures were relatively unchanged from prehypoxic values,
whereas flows to the brainstem and cerebellum nearly doubled and tripled,
respectively. Thus, ischemia is the predominant factor that determines the
topography of tissue injury to major regions of immature rat brain, whereas
metabolic factors (intrinsic vulnerability) may influence the heterogeneous
pattern of damage seen within individual structures.
ARTICLES
Regional cerebral blood flow during hypoxia-ischemia in immature rats
Department of Pediatrics, Milton S. Hershey Medical Center, Pennsylvania State University College of Medicine, Hershey 17033.
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