Palder S B, Huval W, Lelcuk S, Alexander F, Shepro D, Mannick J A, Hechtman H B
Surgery. 1986 Jan;99(1):72-81.
Thromboxane (Tx) inhibition prevents pulmonary leukostasis after acid aspiration. This observation prompted study of polymorphonuclear leukocyte (PMN) accumulations and products of cyclooxygenase. Experiments were conducted with a skin abrasion preparation. Five groups of six rabbits were pretreated intravenously with: (1) placebo, (2) ibuprofen, (3) imidazole and two other Tx syntase inhibitors, (4) OKY 1555, or (5) OKY 046. Zymosan-activated serum (ZAS) and leukotriene B4 were used as chemotaxins and balanced salt solution as control. After pretreatment with placebo, PMN accumulation in leukotriene B4 sites was 2130 +/- 874 PMN/mm3 (mean +/- SD). Pretreatment with ibuprofen, imidazole, or OKY 046 decreased (p less than 0.05) accumulations to 205 +/- 139 PMN/mm3, 485 +/- 387 PMN/mm3, and 504 +/- 260 PMN/mm3, respectively. In ZAS sites, placebo pretreatment led to 2006 +/- 866 PMN/mm3, while the ibuprofen, imidazole, and OKY 046 groups had decreased (p less than 0.05) responses of 295 +/- 218 PMN/mm3, 444 +/- 477 PMN/mm3, and 386 +/- 151 PMN/mm3, respectively. Pretreatment with OKY 1555 did not produce significant reductions in response. Six animals in each group received intradermal injections of the two chemotaxins or Hank's balanced salt solution. Reduction in PMN accumulations after cyclooxygenase and Tx inhibition were similar to those observed in the skin abrasion preparation. Pretreatment with either ibuprofen, imidazole, or OKY 046 resulted in a decreased concentration of Tx in abrasion fluid exudate in response to leukotriene B4, 275 +/- 164 pg/ml, 460 +/- 144 pg/ml, and 440 +/- 260 pg/ml, respectively, as compared with 1168 +/- 380 pg/ml in the placebo group. The reduced responses were not the result of a decrease in regional perfusion as measured by 133Xe washout. The in vitro chemotactic response of PMN to leukotriene B4 and ZAS was unchanged after incubation in either ibuprofen, imidazole, OKY 1555, or OKY 046. These data show that cyclooxygenase and Tx syntase are integrally associated with PMN accumulations.
血栓素(Tx)抑制可预防酸吸入后的肺白细胞淤滞。这一观察结果促使人们对多形核白细胞(PMN)的聚集以及环氧化酶产物进行研究。实验采用皮肤擦伤模型。将五组每组六只兔子静脉注射预处理药物:(1)安慰剂,(2)布洛芬,(3)咪唑和其他两种Tx合成酶抑制剂,(4)OKY 1555,或(5)OKY 046。酵母聚糖激活血清(ZAS)和白三烯B4用作趋化因子,平衡盐溶液用作对照。用安慰剂预处理后,白三烯B4部位的PMN聚集为2130±874个PMN/mm³(平均值±标准差)。用布洛芬、咪唑或OKY 046预处理后,聚集分别降至205±139个PMN/mm³、485±387个PMN/mm³和504±260个PMN/mm³(p<0.05)。在ZAS部位,安慰剂预处理导致2006±866个PMN/mm³,而布洛芬、咪唑和OKY 046组的反应分别降至295±218个PMN/mm³、444±477个PMN/mm³和386±151个PMN/mm³(p<0.05)。用OKY 1555预处理并未使反应显著降低。每组六只动物接受两种趋化因子或汉克平衡盐溶液的皮内注射。环氧化酶和Tx抑制后PMN聚集的减少与皮肤擦伤模型中观察到的相似。用布洛芬、咪唑或OKY 046预处理后,与安慰剂组的1168±380 pg/ml相比,对白三烯B4反应时擦伤液渗出物中Tx浓度分别降至275±164 pg/ml、460±144 pg/ml和440±260 pg/ml。反应降低并非由¹³³Xe洗脱测量的局部灌注减少所致。在布洛芬、咪唑、OKY 1555或OKY 046中孵育后,PMN对白三烯B4和ZAS的体外趋化反应未改变。这些数据表明环氧化酶和Tx合成酶与PMN聚集密切相关。