Rojas A, Padrón J, Caveda L, Palacios M, Moncada S
Center for Pharmaceutical Chemistry, Havana, Cuba.
Biochem Biophys Res Commun. 1993 Mar 15;191(2):441-6. doi: 10.1006/bbrc.1993.1237.
Survival after lipopolysaccharide challenge (LD80, 20 mg.kg-1, i.p.) was significantly enhanced by previous treatment with a microdose of LPS (50 micrograms.kg-1, i.v.). When NG-monomethyl-L-arginine, a specific inhibitor of the formation of nitric oxide from L-arginine, was given 30 minutes before microdose, survival was significantly reduced. When we monitored the serum Tumor Necrosis Factor (TNF) levels in both groups a significant reduction of TNF level after the microdose was observed in mice previously treated with L-NMMA. The ability of L-NNMA to reduce TNF release was dose dependent.
经微量脂多糖(LPS)(50微克·千克-1,静脉注射)预处理后,脂多糖攻击(半数致死剂量80,20毫克·千克-1,腹腔注射)后的存活率显著提高。当在微量给药前30分钟给予L-精氨酸一氧化氮形成的特异性抑制剂Nω-单甲基-L-精氨酸时,存活率显著降低。当我们监测两组小鼠血清肿瘤坏死因子(TNF)水平时,发现先前用L-NMMA处理的小鼠在微量给药后TNF水平显著降低。L-NNMA降低TNF释放的能力呈剂量依赖性。