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首页> 外文期刊>European Journal of Pharmacology: An International Journal >A novel dual regulator of tumor necrosis factor-alpha and interleukin-10 protects mice from endotoxin-induced shock.
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A novel dual regulator of tumor necrosis factor-alpha and interleukin-10 protects mice from endotoxin-induced shock.

机译:一种新型的肿瘤坏死因子-α和白介素10双重调节剂可保护小鼠免受内毒素诱发的休克的侵害。

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摘要

A pyrimidylpiperazine derivative, N-[1-(4-{[4-(pyrimidin-2-yl)piperazin-1-yl]methyl}phenyl)cycloprop yl] acetamide (Y-39041), is a dual cytokine regulator of tumor necrosis factor (TNF)-alpha and interleukin-10 production. Lipopolysaccharide-induced TNF-alpha release in BALB/c mice was inhibited by the oral treatment with the compound at 10-100 mg/kg (about 80% suppression) while interleukin-10 release was augmented (about 10-fold increase at 30 mg/kg). In addition, Y-39041 (30 mg/kg, p.o.) completely protected mice from lipopolysaccharide-induced death by the treatment before and after lipopolysaccharide injection. The finding that Y-39041 suppresses TNF-alpha production and stimulates interleukin-10 production at the same time provides new insights for the treatment of septic shock, rheumatoid arthritis and Crohn's diseases.
机译:嘧啶哌嗪衍生物N- [1-(4-{[4-(嘧啶-2-基)哌嗪-1-基]甲基}苯基}环丙基]乙酰胺(Y-39041)是肿瘤的双重细胞因子调节剂坏死因子(TNF)-α和白介素10的产生。用10-100 mg / kg的化合物口服处理可抑制脂多糖诱导的BALB / c小鼠的TNF-α释放(抑制约80%),而白介素10的释放则增加(30 mg时约增加10倍) /公斤)。此外,通过注射脂多糖前后,Y-39041(30 mg / kg,p.o.)完全保护小鼠免受脂多糖诱导的死亡。 Y-39041抑制TNF-α产生并同时刺激白介素10产生的发现为脓毒性休克,类风湿性关节炎和克罗恩病的治疗提供了新的见解。

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