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European Journal of Cardio-Thoracic Surgery, Vol 11, 973-980, Copyright © 1997 by European Association for Cardio-thoracic Surgery
M Kamler, H Jakob, HA Lehr, MM Gebhard and S Hagl
OBJECTIVE: The clinical complications of extracorporeal circulation (ECC)
have been linked to a systemic activation of cellular and humoral
components and to a dysregulation of the microcirculatory compartment.
Since to date only in vitro methods exist for evaluation, we developed an
animal model to study the effects of ECC on the microcirculation. To
establish the model, we assessed whether these effects are dependent on the
duration of ECC. METHODS: Intravital fluorescence microscopy was used on
the dorsal skinfold chamber preparation in chronically instrumented, awake
Syrian golden hamsters. ECC was realized using a micro-rollerpump and a
silicon tube shunting blood between the carotid artery and the jugular
vein. ECC was performed in three groups for various times (2, 10 and 20
min) after application of heparin at 300 IU/kg body wt. In hamsters, the
application of high-dose heparin releases endothelial bound superoxide
dismutase (SOD), a natural scavenger of oxygen-derived free radicals.
Protocol II assigned two groups receiving heparin at different doses of 50
and 2000 IU/kg body wt. RESULTS: ECC for 2 min served as control to exclude
effects from hemodilution and resulted in a minimal induction of
leukocyte/endothelial cell interaction. Isovolemic ECC for 20 min resulted
in an increase in rolling (from 11 +/- 3 to 38 +/- 20%, mean +/- S.D., P
< 0.05) and adherent leukocytes (from 19 +/- 16 to 215 +/- 145
cells/mm2, mean +/- S.D., P < 0.05) in postcapillary venules.
Microhemodynamic parameters and functional capillary density were not
significantly affected. Arterial blood pressure and heart rate were stable.
Heparin at 2000 IU/kg inhibited post-ECC leukocyte adhesion following ECC,
whereas 50 IU/kg showed no protective effects. CONCLUSIONS:
Leukocyte/endothelial cell interaction, induced by blood contact with
synthetic surfaces, was directly visualized in vivo. The number of adherent
leukocytes was dependent on the duration of ECC. The application of
high-dose heparin followed by release of SOD almost prevented leukocyte
activation, suggesting a formation of oxygen free radicals during ECC. The
new application of the hamster model may allow to study the underlying
pathomechanisms and to develop therapeutic/prophylactic strategies to avert
problems associated with ECC.
ARTICLES
Direct visualization of leukocyte/endothelial cell interaction during extracorporeal circulation (ECC) in a new animal model
Department of Cardiac Surgery, University of Heidelberg, Chirurgische Klinik, Germany.
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