Traykov T, Hadjimitova V, Goliysky P, Ribarov S
Department of Biophysics, Sofia University School of Medicine, Bulgaria.
Gen Physiol Biophys. 1997 Mar;16(1):3-14.
The inhibitory effect of some phenothiazine neuroleptics (chlorpromazine, levomepromazine, thioridazine, promethazine and trifluoperazine) on the ability of rat peritoneal macrophages to produce O2- during phagocytosis was investigated. The superoxide radical release was estimated by measuring the luminol-dependent chemiluminescence (CL). The effect of drugs was studied in the concentration range of 0.1-100 mumol/l. Additional experiments to determine the ability of the drugs to scavenge O2- were carried out. They included measuring the effect of phenothiazines on the luminol-dependent CL in systems with enzymatically (xanthine-xanthine oxidase) and non-enzymatically (KO2) generated O2-. The ability of phenothiazines to scavenge O2- was additionally tested by a "non-luminescence" method in which the superoxide concentration was determined spectrophotometrically by the reduction of nitro blue tetrazolium to formazan. All drugs tested decreased significantly CL of stimulated macrophages at concentrations greater than 1 mumol/l. The C50 values were between 0.45 and 1.74 mumol/l. Also phenothiazines were found to act as scavengers of O2-. However, this effect occurred at significantly higher drug concentrations. The C50 values for 50% scavenging of O2- in systems with different sources of O2- were in the concentration range of 5-160 mumol/l. These results suggested that phenothiazines predominantly affected the ability of macrophages to produce O2- during phagocytosis. The findings may provide some insight into the untoward effects of the drugs tested.
研究了某些吩噻嗪类抗精神病药物(氯丙嗪、左美丙嗪、硫利达嗪、异丙嗪和三氟拉嗪)对大鼠腹腔巨噬细胞吞噬作用过程中产生超氧阴离子(O2-)能力的抑制作用。通过测量鲁米诺依赖性化学发光(CL)来估计超氧阴离子自由基的释放。在0.1 - 100 μmol/L的浓度范围内研究了药物的作用。还进行了额外的实验以确定药物清除O2-的能力。这些实验包括测量吩噻嗪类药物对酶促(黄嘌呤 - 黄嘌呤氧化酶)和非酶促(超氧化钾)产生O2-的体系中鲁米诺依赖性CL的影响。通过“非发光”方法额外测试了吩噻嗪类药物清除O2-的能力,在该方法中,通过将硝基蓝四唑还原为甲臜,用分光光度法测定超氧阴离子浓度。所有测试药物在浓度大于1 μmol/L时均显著降低了刺激巨噬细胞的CL。半数有效浓度(C50)值在0.45至1.74 μmol/L之间。还发现吩噻嗪类药物可作为O2-的清除剂。然而,这种作用在显著更高的药物浓度下才会出现。在具有不同O2-来源的体系中,50%清除O2-的C50值在5 - 160 μmol/L的浓度范围内。这些结果表明,吩噻嗪类药物主要影响巨噬细胞在吞噬作用过程中产生O2-的能力。这些发现可能为所测试药物的不良反应提供一些见解。