Post-ischemic reperfusion impairment, ("no-reflow phenomenon"), was st
udied in rats subjected to 8-30 minutes of global brain ischemia. Duri
ng ischemia, rapid and complete loss of cerebral blood flow, EEG and P
-31-high energy phosphates (ATP/PCr) was observed. Brain intravascular
perfusion defects were examined by injecting carbon black intravenous
ly in a group of rats with stable cardiopulmonary function and in anot
her group subjected to rapid thoracotomy and intraarterial infusion of
the carbon marker. Results indicate that global brain ischemic or non
-ischemic control rats given intraarterial carbon black after thoracot
omy had varying degrees of vessel filling defects in brain resulting i
n "pale tissue areas" suggestive of impaired perfusion (no-reflow). Al
l rats given carbon black intravenously whether global brain ischemic
or not, showed normal cerebrovascular filling of the carbon black and
absence of "pale tissue areas". In addition, post-ischemic cerebral re
perfusion following 8-30 minutes global brain ischemia can reverse neu
roelectric, energy metabolite and cerebral blood flow loss in rats who
se cardiopulmonary function is not compromised. These findings indicat
e that the "no-reflow phenomenon" is an agonal or post-mortem artifact
observed in the presence of cardiopulmonary failure.