Lafuze J E, Weisman S J, Ingraham L M, Butterick C J, Alpert L A, Baehner R L
Ciba Found Symp. 1983;101:130-46. doi: 10.1002/9780470720820.ch9.
Chemoattractants such as N-formylmethionyl leucyl phenylalanine (FMLP) cause neutropenia in vivo. The sequestered neutrophils may block the microvasculature and contribute to respiratory distress. Neutrophils from humans receiving 1600 units vitamin E per day have reduced oxidative activity. To test whether vitamin E attenuates the responses of neutrophils to FMLP in vivo we gave rabbits four daily intramuscular injections of 100 mg vitamin E. Serum levels of the vitamin were 2.34 +/- 0.15 mg% compared to 0.19 +/- 0.04 mg% in control rabbits receiving placebo injections. On the fifth day testing was done before and after injecting FMLP. Variables monitored were the absolute granulocyte count (AGC), systolic, diastolic and mean blood pressures (MBP), heart rate, PO2, PCO2, pH and respiratory rate. When 0.5 microgram FMLP was injected intravenously the AGC decreased (at 2.5 min the percentage change was -89.7 +/- 8.0 with vitamin E and -97.0 +/- 2.7 without vitamin E; P = 0.2). MBP decreased also (% change, -29.0 +/- 13.0 with vitamin E and -36.3 +/- 16.0, without vitamin E). By 15 min recovery was seen (AGC % change, -26.0 +/- 17 with vitamin E and -78.7 +/- 10.5, without vitamin E; P = 0.01; MBP % change, -9.3 +/- 3.8 with vitamin E and -52.3 +/- 10.1 without vitamin E). Chromatographic analysis of serum extracts revealed increases in 6-keto-PGF1 alpha after stimulation. Studies with [3h]thymidine-labelled neutrophils showed that the sequestered cells return to the circulation. Vitamin E might facilitate this return by altering the adherence of neutrophils to endothelium. This possibility was tested by measuring the adherence to cultivated rabbit aorta endothelial monolayers of FMLP-stimulated neutrophils from vitamin E-treated rabbits. The percentage of neutrophils adhering was 32.5 +/- 3.5 with vitamin E and 60.0 +/- 7.1, without vitamin E. Thus vitamin E promotes the return of neutrophils to the circulation after chemotactic challenge and may do so by reducing their adherence to endothelium.
诸如N-甲酰甲硫氨酰亮氨酰苯丙氨酸(FMLP)等趋化因子可在体内导致中性粒细胞减少。被隔离的中性粒细胞可能会阻塞微血管并导致呼吸窘迫。每天摄入1600单位维生素E的人的中性粒细胞氧化活性降低。为了测试维生素E是否能在体内减弱中性粒细胞对FMLP的反应,我们给兔子每日进行4次100毫克维生素E的肌肉注射。维生素的血清水平为2.34±0.15毫克%,而接受安慰剂注射的对照兔子为0.19±0.04毫克%。在第五天,在注射FMLP之前和之后进行测试。监测的变量包括绝对粒细胞计数(AGC)、收缩压、舒张压和平均血压(MBP)、心率、PO2、PCO2、pH值和呼吸频率。静脉注射0.5微克FMLP后,AGC下降(2.5分钟时,维生素E组的百分比变化为-89.7±8.0,无维生素E组为-97.0±2.7;P = 0.2)。MBP也下降(百分比变化,维生素E组为-29.0±13.0,无维生素E组为-36.3±16.0)。到15分钟时可见恢复(AGC百分比变化,维生素E组为-26.0±17,无维生素E组为-78.7±10.5;P = 0.01;MBP百分比变化,维生素E组为-9.3±3.8,无维生素E组为-52.3±10.1)。血清提取物的色谱分析显示刺激后6-酮-PGF1α增加。用[3H]胸腺嘧啶标记的中性粒细胞进行的研究表明,被隔离的细胞会回到循环中。维生素E可能通过改变中性粒细胞与内皮的黏附来促进这种回归。通过测量来自维生素E处理兔子的FMLP刺激的中性粒细胞对培养的兔主动脉内皮单层的黏附来测试这种可能性。维生素E组中性粒细胞黏附的百分比为32.5±3.5,无维生素E组为60.0±7.1。因此,维生素E在趋化刺激后促进中性粒细胞回到循环中,并且可能通过减少它们与内皮的黏附来实现。