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(Stroke. 2002;33:606.)
© 2002 American Heart Association, Inc.

Original Contributions

Penumbral Microcirculatory Changes Associated With Peri-infarct Depolarizations in the Rat

Elisabeth Pinard, PhD; Hélène Nallet, PhD; Eric T. MacKenzie, PhD; Jacques Seylaz, PhD Simon Roussel, PhD

From Laboratoire de Recherches Cérébrovasculaires, CNRS UPR 646, Université Paris 7, IFR 6 (E.P., J.S.), and CNRS UMR 6551, Université de Caen, IFR 47 (H.N., E.T.M., S.R.), Paris, France.

Correspondence to Dr Elisabeth Pinard, Laboratoire de Recherches Cérébrovasculaires, 10 Avenue de Verdun, 75010 Paris, France. E-mail pinard{at}ext.jussieu.fr

Background and Purpose— This study was designed to investigate the influence of peri-infarct depolarization elicited by occlusion of the middle cerebral artery on the dynamics of the microcirculation.

Methods— The microcirculation in the frontoparietal cortex of 9 rats was visualized in real time through a closed cranial window with the use of laser-scanning confocal fluorescence microscopy combined with intravenous fluorescein isothiocyanate (FITC)–dextran and FITC-labeled erythrocytes. The direct current potential/electrocorticogram was continuously monitored. Intraluminal focal ischemia was induced for 2 hours in 6 rats anesthetized with halothane and mechanically ventilated. Reperfusion was monitored for 1 hour. Three rats underwent sham operation. Brains were removed 24 hours after occlusion and processed for histology.

Results— In control conditions, the velocity of fluorescent erythrocytes through capillaries was 0.51±0.19 mm/s (mean±SD), and the diameter of the arterioles studied was 33±12 µm. Under ischemia, erythrocyte velocity through capillaries was significantly decreased to 0.33±0.14 mm/s, while arteriole diameter did not change significantly. During spontaneous peri-infarct depolarizations, arteriole diameter was significantly increased (119±23% of baseline), while capillary erythrocyte velocity was further decreased by 14±34%. The direction of arteriolar blood flow episodically and transiently reversed during approximately half of the peri-infarct depolarizations. The decrease in capillary erythrocyte velocity was more pronounced (23±37%) in these cases. After reperfusion, the microcirculatory variables rapidly returned to baseline. All rats in the ischemic group had infarcts 24 hours after occlusion.

Conclusions— Peri-infarct depolarization has an adverse influence on penumbral microcirculation, reducing capillary perfusion by erythrocytes, despite dilatation of arterioles. These findings suggest that a steal phenomenon contributes to the deleterious effect of these depolarizations.

Key Words: cerebral ischemia, focal • microcirculation • microscopy, fluorescence • penumbra • rats

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