首页> 外文期刊>International immunopharmacology >Paeoniflorin improves survival in LPS-challenged mice through the suppression of TNF-alpha and IL-1beta release and augmentation of IL-10 production.
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Paeoniflorin improves survival in LPS-challenged mice through the suppression of TNF-alpha and IL-1beta release and augmentation of IL-10 production.

机译:eon药苷通过抑制TNF-α和IL-1beta的释放以及增加IL-10的产生来提高LPS攻击小鼠的存活率。

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摘要

Lipopolysaccharide (LPS) plays an important role in Gram-negative bacteria-induced sepsis and multiple organ dysfunction syndrome, which are still the leading cause of high mortality in intensive care units. Although paeoniflorin (Pae) has reportedly exhibited anti-inflammatory effect and protection against immunological liver injury in mice, it is not known whether Pae improve survival in endotoxemic mice. The purpose of this study was to determine the effect of Pae on the mortality, multiple organ dysfunction and cytokine production in lipopolysaccharide (LPS)-treated mice. We found that pretreatment with Pae decreased mortality, reduced lung and kidney injury, decreased serum creatinine level and improve systolic function of heart in mice challenged with LPS. Further experiments showed that Pae inhibited LPS-stimulated tumor necrosis factor-alpha (TNF-alpha) and interleukin-1beta (IL-1beta) release and promoted LPS-induced interleukin-10 (IL-10) production. Our results indicate that Pae protects mice against lethal LPS challenge, at least in part, through inhibiting TNF-alpha and IL-1beta production and accelerating IL-10 expression.
机译:脂多糖(LPS)在革兰氏阴性菌引起的败血症和多器官功能障碍综合症中起着重要作用,这仍然是重症监护病房高死亡率的主要原因。尽管据报道pa药苷(Pae)在小鼠中表现出抗炎作用和对免疫性肝损伤的保护作用,但尚不清楚Pae是否能提高内毒素血症小鼠的存活率。这项研究的目的是确定Pae对脂多糖(LPS)处理的小鼠的死亡率,多器官功能障碍和细胞因子产生的影响。我们发现用Pae进行预处理可以降低LPS攻击的小鼠的死亡率,减少肺和肾脏损伤,降低血清肌酐水平并改善心脏的收缩功能。进一步的实验表明,Pae抑制LPS刺激的肿瘤坏死因子-α(TNF-alpha)和白介素1β(IL-1beta)的释放,并促进LPS诱导的白介素10(IL-10)的产生。我们的结果表明,Pae至少部分通过抑制TNF-α和IL-1beta的产生并加速IL-10的表达,保护小鼠免受LPS的致命攻击。

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