Stroke, Vol 20, 1377-1382, Copyright © 1989 by American Heart Association
J de Boer, HC Klein, F Postema, KG Go and J Korf
We investigated the earliest time at which irreversible damage takes place
after hypoxia-ischemia in the Levine preparation of rats. In 60 rats
anesthetized with chloral hydrate and maintained at one of three body
temperatures, we unilaterally ligated the left common carotid artery and
placed electrodes in the striatum to measure impedance (reflecting the
extracellular space) during hypoxia, recovery, and/or cardiac arrest. We
measured blood gases and pH at regular intervals during hypoxia in 47 rats
and assessed blood-brain barrier function with Evans blue and tissue damage
using Na+:K+ ratios. Shortly after hypoxia, impedance normalized in 24 rats
without brain damage (normal Na+:K+ ratios, 4 hours of recovery). Sustained
elevation of striatal impedance during recovery in six rats was related to
an elevated Na+:K+ ratio and a disrupted blood-brain barrier. Damage was
not obviously related to blood gases, pH, or the net reduction of the
extracellular space during hypoxia. Hypothermia in 17 rats prevented
impedance changes, and no striatal damage was found. Thus, irreversible
brain damage very likely occurs during or very shortly after hypoxia.
Persistent reduction of the extracellular space indicates tissue damage and
can be used to monitor potential in vivo therapeutic measures.
ARTICLES
Rat striatal cation shifts reflecting hypoxic-ischemic damage can be predicted by on-line impedance measurements
Department of Biological Psychiatry, University Hospital, Groningen, The Netherlands.
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