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一氧化氮途径在低剂量脂多糖对致死性内毒素血症的保护作用中的角色。

Role of nitric oxide pathway in the protection against lethal endotoxemia afforded by low doses of lipopolysaccharide.

作者信息

Rojas A, Padrón J, Caveda L, Palacios M, Moncada S

机构信息

Center for Pharmaceutical Chemistry, Havana, Cuba.

出版信息

Biochem Biophys Res Commun. 1993 Mar 15;191(2):441-6. doi: 10.1006/bbrc.1993.1237.

Abstract

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.

摘要

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。

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