Synthetic Colloids Attenuate Leukocyte-Endothelial Interactions by Inhibition of Integrin Function

Author:

Nohé Boris1,Johannes Tanja2,Reutershan Jörg3,Rothmund Albert4,Haeberle Helene A.1,Ploppa Annette1,Schroeder Torsten H.1,Dieterich Hans-Juergen5

Affiliation:

1. Staff Anesthesiologist.

2. Staff Anesthesiologist, Department of Anaesthesiology and Intensive Care Medicine, University Hospital, Eberhard-Karls University Tuebingen. Research Associate, Department of Physiology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

3. Staff Anesthesiologist, Department of Anaesthesiology and Intensive Care Medicine, University Hospital, Eberhard-Karls University Tuebingen. Research Associate, Cardiovascular Research Center, University of Virginia Health System, Charlottesville, Virginia.

4. Research Fellow, Department of Anesthesiology and Intensive Care Medicine, University Hospital, Eberhard-Karls University Tuebingen. Otolaryngologist, Deparment of Oto-Rhino-Laryngology, Städtisches Klinikum Karlsruhe, Germany.

5. Assistant Professor of Anesthesiology, Department of Anaesthesiology and Intensive Care Medicine, University Hospital, Eberhard-Karls University Tuebingen.

Abstract

Background It has been suspected that synthetic colloids may interfere with leukocyte adhesion by down-regulation of endothelial cell adhesion molecules. Although inhibition of endothelial inflammation might reduce leukocyte-related tissue injury, the same mechanism may be detrimental for host defense during severe infection. Regarding the widespread use of colloids, the authors performed a laboratory investigation to determine the mechanisms by which synthetic colloids interfere with leukocyte-endothelial interactions. Methods Adhesion molecule expression on native and cytokine-activated endothelium from umbilical veins was measured after pretreatment with gelatin and various preparations of dextran or hydroxyethyl starch. Inhibition of neutrophil adhesion to activated endothelium was examined in a flow chamber by perfusion of untreated and colloid-treated neutrophils over colloid-pretreated endothelium at 2 dyn/cm. Comparisons were made between untreated controls, colloid-pretreated endothelium, and colloid-cotreated neutrophils. Results Intercellular adhesion molecule 1, vascular cell adhesion molecule 1, E-selectin, and P-selectin were not attenuated by any colloid. Accordingly, colloid pretreatment of endothelium alone did not reduce neutrophil adhesion. In contrast, when neutrophils were cotreated by addition of colloids to the perfusate immediately before perfusion, adhesion decreased by 31-51% (P < 0.05) regardless of the colloid type. As indicated by the twofold increased rolling fractions, this reduction was due to an inhibition of neutrophil integrins. Conclusions This study shows that synthetic colloids inhibit neutrophil adhesion by a neutrophil-dependent mechanism rather than interfering with endothelial cell activation. This suggests that inhibition of leukocyte sequestration by volume support is a common and transient phenomenon depending on the colloid concentration in plasma.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine

Reference61 articles.

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