首页> 美国卫生研究院文献>Drug Design Development and Therapy >n-Butanol extract from Folium isatidis inhibits lipopolysaccharide-induced inflammatory cytokine production in macrophages and protects mice against lipopolysaccharide-induced endotoxic shock
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n-Butanol extract from Folium isatidis inhibits lipopolysaccharide-induced inflammatory cytokine production in macrophages and protects mice against lipopolysaccharide-induced endotoxic shock

机译:大青叶中正丁醇提取物抑制巨噬细胞中脂多糖诱导的炎性细胞因子的产生并保护小鼠免受脂多糖诱导的内毒素性休克

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摘要

Sepsis, which is caused by severe infection, is an important cause of mortality, but effective clinical treatment against sepsis is extremely limited. As the main component of the outer membrane of Gram-negative bacteria, lipopolysaccharide (LPS) plays a major role in inflammatory responses. Studies have shown beneficial pharmacological effects for Folium isatidis. The present study further illuminated the effects of n-butanol extract from Folium isatidis in LPS-induced septic shock and identified the main active chemical components. Our study showed that pretreatment with n-butanol extract from Folium isatidis not only significantly inhibited LPS-induced tumor necrosis factor-α and interleukin-6 production but also markedly and dose dependently enhanced the recruitment of MyD88, the phosphorylation of extracellular signal-regulated kinase, and the degradation of IκB-α. Additionally, the extract exhibited dramatic protective effects against lung injury and death in mice with septic shock. Eight main active compounds were identified, including organic acids, glycoside, indolinones, and flavonoids. These findings provide a perspective on the respiratory protection offered by n-butanol extract from Folium isatidis in LPS-induced sepsis and outline a novel therapeutic strategy for the treatment of sepsis.
机译:由严重感染引起的败血症是导致死亡的重要原因,但是针对败血症的有效临床治疗极为有限。作为革兰氏阴性细菌外膜的主要成分,脂多糖(LPS)在炎症反应中起主要作用。研究表明,板蓝根具有有益的药理作用。本研究进一步阐明了板蓝根正丁醇提取物在LPS引起的败血性休克中的作用,并确定了其主要活性化学成分。我们的研究表明,用板蓝根正丁醇提取物预处理不仅显着抑制LPS诱导的肿瘤坏死因子-α和白介素6的产生,而且显着和剂量依赖性地增强了MyD88的募集,即细胞外信号调节激酶的磷酸化,以及IκB-α的降解。另外,该提取物对败血性休克小鼠表现出显着的抗肺损伤和死亡的保护作用。确定了八个主要活性化合物,包括有机酸,糖苷,吲哚满酮和类黄酮。这些发现为板蓝根中正丁醇提取物对LPS诱导的脓毒症的呼吸保护提供了一个观点,并概述了一种新型的脓毒症治疗策略。

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