Hoffer E, Shenker L, Baum Y, Tabak A
Israel Poison Information Center, Rambam Medical Center, Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Free Radic Biol Med. 1997;22(3):567-72. doi: 10.1016/s0891-5849(96)00385-1.
The present work is focused on the formation of the inflammatory mediator leukotriene B4 (LTB4) in the lungs of paraquat (PQ)-intoxicated rats. The levels of LTB4 and the number of neutrophils in lung lavages of PQ-intoxicated rats, measured 12 h after 30 mg/kg PQ, increased significantly compared with those of control animals; administration of 50 mg/kg IP N-acetylcysteine (NAC), 8 h after PQ, inhibited this effect. The release of LTB4 from alveolar macrophages (AM) or alveolar epithelial type II cells from healthy animals incubated with PQ and/or NAC did not offer' an explanation for the effect of these chemicals on LTB4 in the bronchoalveolar lavage fluid (BALF). The PQ-enhanced, NAC-inhibited release of arachidonic acid (AA) by alveolar epithelial type II cells did, however, explain our in vivo results, when one assumes that the AM synthesize their 5-lipoxygenase products from alveolar epithelial cell-derived AA, an hypothesis demonstrated already by other researchers.
目前的工作聚焦于百草枯(PQ)中毒大鼠肺中炎症介质白三烯B4(LTB4)的形成。在给予30mg/kg PQ 12小时后,PQ中毒大鼠肺灌洗液中LTB4的水平和中性粒细胞数量与对照动物相比显著增加;在PQ给药8小时后腹腔注射50mg/kg N-乙酰半胱氨酸(NAC)可抑制这种效应。用PQ和/或NAC孵育健康动物的肺泡巨噬细胞(AM)或II型肺泡上皮细胞后,这些细胞释放LTB4的情况并不能解释这些化学物质对支气管肺泡灌洗液(BALF)中LTB4的影响。然而,如果假设AM从肺泡上皮细胞衍生的花生四烯酸(AA)合成其5-脂氧合酶产物(其他研究人员已证明这一假说),那么II型肺泡上皮细胞因PQ增强、NAC抑制而释放AA的情况确实可以解释我们的体内实验结果。