Norrby K, Andersson R G
Virchows Arch B Cell Pathol Incl Mol Pathol. 1984;46(1-2):83-91. doi: 10.1007/BF02890298.
We investigated whether the mitogenic response induced by local mast-cell secretion in the rat mesentery was affected by suppression of phospholipase A2, lipoxygenase, or cyclooxygenase in arachidonic acid metabolism. Enzyme inhibitor was given in a single intravenous dose 5 min before intraperitoneal injection of the mast-cell secretagogue 48/80. Mepacrine, a phospholipase A2 inhibitor, suppressed the generation of both leukotrienes (SRS) and prostaglandins (PG), whereas the lipoxygenase inhibitor BW 755C reduced the generation of SRS, and the cyclooxygenase inhibitor indomethacin significantly suppressed the generation of PG. None of the enzyme inhibitors affected the basal mesenteric histamine content or histamine release in the mesentery after exposure to 48/80, and none of them affected mast-cell-mediated mitogenesis in the mesentery as judged by specific DNA activity and mitosis counting. The stimulation of DNA synthesis and mitosis initiated by secreting mast cells is apparently not mediated or modulated by synthesis of leukotrienes, prostaglandins, or other known arachidonic acid metabolites.
我们研究了大鼠肠系膜中局部肥大细胞分泌所诱导的促有丝分裂反应是否会受到花生四烯酸代谢中磷脂酶A2、脂氧合酶或环氧化酶抑制的影响。在腹腔注射肥大细胞促分泌剂48/80前5分钟,静脉注射单剂量的酶抑制剂。磷脂酶A2抑制剂米帕林抑制了白三烯(SRS)和前列腺素(PG)的生成,而脂氧合酶抑制剂BW 755C减少了SRS的生成,环氧化酶抑制剂吲哚美辛显著抑制了PG的生成。在暴露于48/80后,这些酶抑制剂均未影响肠系膜中组胺的基础含量或组胺释放,并且根据特异性DNA活性和有丝分裂计数判断,它们均未影响肥大细胞介导的肠系膜有丝分裂。分泌性肥大细胞引发的DNA合成和有丝分裂刺激显然不是由白三烯、前列腺素或其他已知花生四烯酸代谢产物的合成介导或调节的。