Jorens P G, Van Overveld F J, Bult H, Vermeire P A, Herman A G
Department of Pulmonary Medicine, UIA, University of Antwerp, Wilrijk, Belgium.
Eur J Pharmacol. 1991 Aug 6;200(2-3):205-9. doi: 10.1016/0014-2999(91)90573-9.
Rat alveolar and pleural macrophages incubated with lipopolysaccharide, opsonized zymosan or recombinant interferon-gamma, but not with recombinant tumor necrosis factor-alpha, produced nitrite dose and time dependently. This production depends on the presence and amount of L-arginine in the culture medium. The precursor of the nitrite was demonstrated as being nitric oxide, by bleaching of ferredoxin at 410 nm when added to the culture medium. Addition of NG-monomethyl-L-arginine, an inhibitor of nitric oxide synthesis, and cycloheximide, a protein synthesis inhibitor, to the medium resulted in a decrease of nitrite production. Glucocorticoids were able to block the induction of nitrite production in alveolar macrophages. These data indicate that pulmonary macrophages are capable of secreting L-arginine-derived nitrogen oxides.
用脂多糖、调理酵母聚糖或重组干扰素-γ培养的大鼠肺泡巨噬细胞和胸膜巨噬细胞,而非用重组肿瘤坏死因子-α培养的细胞,会剂量和时间依赖性地产生亚硝酸盐。这种产生取决于培养基中L-精氨酸的存在和含量。当加入培养基时,通过在410nm处使铁氧化还原蛋白褪色,证明亚硝酸盐的前体是一氧化氮。向培养基中添加一氧化氮合成抑制剂NG-单甲基-L-精氨酸和蛋白质合成抑制剂环己酰亚胺会导致亚硝酸盐产生减少。糖皮质激素能够阻断肺泡巨噬细胞中亚硝酸盐产生的诱导。这些数据表明肺巨噬细胞能够分泌L-精氨酸衍生的氮氧化物。