Abstract
Summary: We have studied the influence of clinical concentrations of propofol (2,6-diisopropylphenol), emulsified propofol (Diprivan) and the emulsifier of propofol (Intralipid 10%) on random and chemotactic locomotion of human polymorphonuclear leucocytes in an agarose assay. Random locomotion was decreased (P < 0.001) to a similar extent by the three drugs. Concentrations of propofol 2.5 μg ml-1 and greater, and of Diprivan 3.33 μg ml-1 and greater, also reduced chemotaxis (P < 0.05) against both zymosan-activated human serum (C5a) and N-formyl-methionyl-leucylphenylalanine (FMLP), used as chemoattractants. Intralipid reduced chemotaxis towards C5a but not towards FMLP. We conclude that propofol in clinically relevant concentrations may adversely affect leucocyte locomotion in vitro. © 1993 British Journal of Anaesthesia.
Author supplied keywords
Cite
CITATION STYLE
Jensen, A. G., Dahlgren, C., & Eintrei, C. (1993). Propofol decreases random and chemotactic stimulated locomotion of human neutrophils In vitro. British Journal of Anaesthesia, 70(1), 99–100. https://doi.org/10.1093/bja/70.1.99
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.