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The influence of propofol on P‐selectin expression and nitric oxide production in re‐oxygenated human umbilical vein endothelial cells
Author(s) -
Corcoran T. B.,
O'Shea A.,
Engel A.,
Shorten G. D.
Publication year - 2006
Publication title -
acta anaesthesiologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.738
H-Index - 107
eISSN - 1399-6576
pISSN - 0001-5172
DOI - 10.1111/j.1399-6576.2006.00955.x
Subject(s) - nitric oxide , umbilical vein , medicine , propofol , e selectin , inflammation , endothelial stem cell , endothelium , pharmacology , p selectin , hypoxia (environmental) , lipopolysaccharide , oxygenation , anesthesia , immunology , in vitro , biochemistry , cell adhesion , platelet , biology , chemistry , cell , platelet activation , oxygen , organic chemistry
Background: Reperfusion injury is characterized by free radical production and endothelial inflammation. Neutrophils mediate much of the end‐organ injury that occurs, requiring P‐selectin‐mediated neutrophil–endothelial adhesion, and this is associated with decreased endothelial nitric oxide production. Propofol has antioxidant properties in vitro which might abrogate this inflammation. Methods: Cultured human umbilical vein endothelial cells were exposed to 20 h of hypoxia and then returned to normoxic conditions. Cells were treated with saline, Diprivan 5 µg/l or propofol 5 µg/l for 4 h after re‐oxygenation and were then examined for P‐selectin expression and supernatant nitric oxide concentrations for 24 h. P‐selectin was determined by flow cytometry, and culture supernatant nitric oxide was measured as nitrite. Results: In saline‐treated cells, a biphasic increase in P‐selectin expression was demonstrated at 30 min ( P = 0.01) and 4 h ( P = 0.023) after re‐oxygenation. Propofol and Diprivan prevented these increases in P‐selectin expression ( P < 0.05). Four hours after re‐oxygenation, propofol decreased endothelial nitric oxide production ( P = 0.035). Conclusion: This is the first study to demonstrate an effect of propofol upon endothelial P‐selectin expression. Such an effect may be important in situations of reperfusion injury such as cardiac transplantation and coronary artery bypass surgery. We conclude that propofol attenuates re‐oxygenation‐induced endothelial inflammation in vitro .