Nilsson E, Andersson T, Fällman M, Rosendahl K, Palmblad J
Department of Medicine, Karolinska Institute, Sweden.
J Infect Dis. 1992 Oct;166(4):854-60. doi: 10.1093/infdis/166.4.854.
The generation of oxygen radicals by polymorphonuclear leukocytes (PMNL) plays a pivotal role for host defense. Since ethanol reduced FMLP- but not PMA-induced superoxide ion (O2-) formation by PMNL, the effects of ethanol on second messenger systems in PMNL were studied. FMLP induced a biphasic rise in cytosolic calcium concentrations, [Ca2+]i. Ethanol treatment abolished the second phase (believed to reflect Ca2+ influx), an effect also observed in PMNL treated with La3+ or suspended in Ca(2+)-free buffer. The FMLP-induced inositol trisphosphate generation was unaffected by ethanol, whereas diacylglycerol formation was, as expected, markedly reduced. Propranolol, an inhibitor of diacylglycerol formation from phosphatidic acid, caused a prolonged transmembrane influx of Ca2+ and partially reversed the inhibitory effect of ethanol on FMLP-induced O2- production. Thus, the ability of ethanol to inhibit FMLP-induced O2- generation in neutrophils seems to be due to both impaired influx of Ca2+ across the plasma membrane and reduced phospholipase D-mediated generation of phosphatidic acid.
多形核白细胞(PMNL)产生氧自由基对宿主防御起着关键作用。由于乙醇可降低PMNL由N-甲酰甲硫氨酰-亮氨酰-苯丙氨酸(FMLP)诱导而非佛波酯(PMA)诱导的超氧阴离子(O2-)形成,因此研究了乙醇对PMNL中第二信使系统的影响。FMLP可诱导细胞溶质钙浓度([Ca2+]i)出现双相升高。乙醇处理消除了第二阶段(认为反映Ca2+内流),在用La3+处理或悬浮于无Ca2+缓冲液中的PMNL中也观察到这种效应。FMLP诱导的肌醇三磷酸生成不受乙醇影响,而二酰基甘油形成如预期的那样明显减少。普萘洛尔是一种从磷脂酸生成二酰基甘油的抑制剂,它可导致Ca2+跨膜内流延长,并部分逆转乙醇对FMLP诱导的O2-产生的抑制作用。因此,乙醇抑制中性粒细胞中FMLP诱导的O2-生成的能力似乎是由于跨质膜的Ca2+内流受损以及磷脂酶D介导的磷脂酸生成减少。