Heine J, Leuwer M, Scheinichen D, Arseniev L, Jaeger K, Piepenbrock S
Department of Anaesthesiology, Hannover Medical School.
Br J Anaesth. 1996 Sep;77(3):387-92. doi: 10.1093/bja/77.3.387.
Exposure of neutrophils to anaesthetic agents may alter their functional characteristics and in patients undergoing long-term sedation this may be clinically relevant. We have investigated the in vitro influence of propofol, thiopentone, methohexitone and midazolam on phorbol 12-myristate 13-acetate (PMA)-induced respiratory burst of neutrophils by the intracellular oxidative transformation of dihydrorhodamine-123 to the fluorescent dye rhodamine-123 via flow cytometry. We tested in vitro concentrations similar to sedating, anaesthetic, 10-fold sedating and 10-fold anaesthetic plasma concentrations. All drugs showed similar inhibition of respiratory burst at sedating concentrations (1-6%). At anaesthetic concentrations, propofol produced significantly higher mean inhibition (7.3%) compared with thiopentone (4.5%) and methohexitone (0.9%). At 10-fold anaesthetic concentrations inhibition of respiratory burst by propofol was almost complete (90.8%) and significantly higher than that by thiopentone (29.2%) and methohexitone (1.8%). Methohexitone and midazolam had only minimal effects at all concentrations. The effect of the solvent of propofol (10% Intralipid) was similar to that of propofol. Thus suppression of respiratory burst of neutrophils by propofol may be caused by this lipid carrier.
中性粒细胞暴露于麻醉剂可能会改变其功能特性,对于接受长期镇静的患者而言,这可能具有临床相关性。我们通过流式细胞术,研究了丙泊酚、硫喷妥钠、美索比妥和咪达唑仑对佛波酯12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)诱导的中性粒细胞呼吸爆发的体外影响,该过程通过二氢罗丹明-123向荧光染料罗丹明-123的细胞内氧化转化来实现。我们测试了与镇静、麻醉、10倍镇静和10倍麻醉血浆浓度相似的体外浓度。所有药物在镇静浓度下均表现出相似的呼吸爆发抑制作用(1 - 6%)。在麻醉浓度下,与硫喷妥钠(4.5%)和美索比妥(0.9%)相比,丙泊酚产生的平均抑制作用显著更高(7.3%)。在10倍麻醉浓度下,丙泊酚对呼吸爆发的抑制几乎完全(90.8%),且显著高于硫喷妥钠(29.2%)和美索比妥(1.8%)。美索比妥和咪达唑仑在所有浓度下的影响都极小。丙泊酚的溶剂(10%英脱利匹特)的作用与丙泊酚相似。因此,丙泊酚对中性粒细胞呼吸爆发的抑制可能是由这种脂质载体引起的。