Sevoflurane modulates the release of reactive oxygen species, myeloperoxidase, and elastase in human whole blood: Effects of different stimuli on neutrophil response to volatile anesthetic in vitro

被引:5
|
作者
Minguet, Gregory [1 ]
Franck, Thierry [2 ,3 ]
Joris, Jean [1 ]
Serteyn, Didier [2 ,3 ]
机构
[1] Ctr Hosp Univ Liege, Dept Anesthesia & Intens Care Med, Domaine Univ Sart Tilman,Batiment B35, B-4000 Liege, Belgium
[2] Univ Liege, Ctr Oxygen Res & Dev, Inst Chem B6a, Liege, Belgium
[3] Univ Liege, Fac Vet Med, Dept Clin Sci Anesthesiol & Equine Surg, Liege, Belgium
关键词
elastase; halogenated anesthetics; inflammatory response; myeloperoxidase; polymorphonuclear neutrophils; reactive oxygen species; sevoflurane; TUMOR-NECROSIS-FACTOR; ISCHEMIA-REPERFUSION INJURY; ONE-LUNG VENTILATION; INFLAMMATORY RESPONSE; RESPIRATORY BURST; ACTIVATION; ISOFLURANE; SURGERY; DYSFUNCTION; MECHANISMS;
D O I
10.1177/0394632017739530
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Volatile anesthetics have been shown to modulate polymorphonuclear neutrophil (PMN) functions. The aim of this study was to examine the impact of clinically relevant concentrations of sevoflurane (SEVO), a volatile anesthetic, on the release of reactive oxygen species (ROS), myeloperoxidase (MPO), and elastase (EL) from human activated PMNs. For this purpose, samples of whole blood were collected from healthy volunteers and exposed in vitro to 2.3% or 4.6% SEVO in air. To assess for a stimulus-dependent effect of the volatile anesthetic, PMNs were activated using different validated protocols. Artificial stimulation of neutrophils involved either a combination of cytochalasin B (CB) and N-formyl-methionyl-leucyl-phenylalanine (fMLP) or phorbol 12-myristate 13-acetate (PMA). In addition, a combination of lipopolysaccharide (LPS) and tumor necrosis factor alpha (TNF-) was also tested as a natural activation mean of PMNs. The production of ROS by PMNs was assessed by L-012 chemiluminescence. Total MPO and EL released in supernatant were measured by enzyme-linked immunosorbent assay (ELISA). Furthermore, degranulation of the active fraction of MPO was also measured by specific immunological extraction followed by enzymatic detection (SIEFED). Overall, SEVO enhanced the release of ROS, MPO, and EL following artificial stimulation of PMNs but the volatile anesthetic inhibited the degranulation of active MPO and EL after neutrophil exposure to LPS and TNF-. This study highlighted that the effect of SEVO on activated PMNs is dependent on the conditions of cell stimulation. These properties should be taken into consideration in future studies investigating immunomodulatory effects of volatile anesthetics.
引用
收藏
页码:362 / 370
页数:9
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