Zipser R D, Nast C C, Lee M, Kao H W, Duke R
Gastroenterology. 1987 Jan;92(1):33-9. doi: 10.1016/0016-5085(87)90836-5.
Leukotriene B4, a proinflammatory compound, recently has been identified as the major metabolite of arachidonic acid in tissue incubations of human and animal colitis. To determine the relationship of inflammation to the in vivo production of leukotrienes, rabbit colitis was induced by formalin enema followed by intravenous infusion of immune complexes, and serial samples were collected by rectal dialysis. Leukotrienes B4 and C4 were measured by radioimmunoassay after high-pressure liquid chromatography. Prostaglandin E2 was assayed after Sephadex chromatography. Leukotrienes were not detected in control animals. Eicosanoid production progressively increased during development of inflammation and correlated with severity of inflammatory cell infiltration (p less than 0.01). Methylprednisolone decreased prostaglandin E2 but did not significantly reduce leukotrienes or inflammation. These data demonstrate that in vivo production of leukotrienes B4 and C4 correlates with indices of inflammation, consistent with the concept that these eicosanoids contribute to the inflammation of colitis.
白三烯B4是一种促炎化合物,最近已被确定为人类和动物结肠炎组织培养中花生四烯酸的主要代谢产物。为了确定炎症与白三烯体内产生之间的关系,通过福尔马林灌肠诱导兔结肠炎,随后静脉输注免疫复合物,并通过直肠透析收集系列样本。高压液相色谱后通过放射免疫测定法测量白三烯B4和C4。葡聚糖凝胶色谱后测定前列腺素E2。对照动物中未检测到白三烯。在炎症发展过程中类花生酸的产生逐渐增加,并与炎症细胞浸润的严重程度相关(p<0.01)。甲基泼尼松龙降低了前列腺素E2,但并未显著降低白三烯或炎症。这些数据表明,白三烯B4和C4的体内产生与炎症指标相关,这与这些类花生酸促成结肠炎炎症的概念一致。