Induction of inducible nitric oxide synthase by lipopolysaccharide/interferon gamma and sepsis down-regulates 5-lipoxygenase metabolism in murine alveolar macrophages

被引:20
作者
Coffey, MJ [1 ]
Phare, SM [1 ]
Peters-Golden, M [1 ]
机构
[1] Univ Michigan, Med Ctr, Div Pulm & Crit Care Med, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
eicosanoid; endotoxin; leukotriene; peritonitis; reactive nitrogen intermediate;
D O I
10.1080/01902140490476391
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Pretreatment with lipopolysaccharide (LPS) suppresses rat alveolar macrophage leukotriene synthesis in a nitric oxide (NO)-dependent mechanism. The authors examined the effect of NO on alveolar macrophage leukotriene synthesis following in vitro and in vivo models of sepsis. Treatment of alveolar macrophages from inducible NO synthase (iNOS) wild-type but not knock-out mice with LPS inhibited leukotriene synthesis. iNOS was induced early in alveolar macrophages from cecal ligation and puncture rats and mice compared to sham animals with associated reduced leukotriene synthesis. iNOS knock-out mice were protected from the decrease in alveolar macrophage 5-lipoxygenase metabolism. iNOS regulates alveolar macrophage 5-lipoxygenase metabolism following endotoxin exposure.
引用
收藏
页码:615 / 633
页数:19
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