Stroke, Vol 15, 46-50, Copyright © 1984 by American Heart Association
JI Sage, RL Van Uitert and TE Duffy
Brain unidirectional extraction and flux of leucine were measured
simultaneously with cerebral blood flow (CBF) at various times after
transient global cerebral ischemia in the rat. The results permit an
evaluation of blood-brain barrier permeability in the postischemic period
independent of alterations in CBF at the time of measurement. Leucine
extraction was higher (p less than 0.001) than that of CBF- matched
controls at 15 min and 6 hr after 30 min of global cerebral ischemia, but
was not different from control at 30 min and 1 h after ischemia. Leucine
flux into brain was increased only at 15 min after reperfusion of the
brain. Cerebral edema occurs 15-30 min after reperfusion in this ischemia
model, but the permeability of the blood- brain barrier to large molecules
is unaltered during this period (Petito et al: J Neuropath Exp Neurol
41:423-436, 1982). Increased barrier permeability to small molecules such
as leucine may contribute to the production of this early postischemic
edema.
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Early changes in blood brain barrier permeability to small molecules after transient cerebral ischemia
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