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武田-143242 通过降低猪腹膜炎中的细胞因子来提高存活率。

TAKEDA-143242 increased survival via reduced cytokines in porcine peritonitis.

机构信息

Department of Medicine, Sections of Cardiology and Critical Care, Rush Medical College, Chicago, Illinois, USA.

出版信息

J Surg Res. 2011 Apr;166(2):e165-73. doi: 10.1016/j.jss.2010.09.031. Epub 2010 Nov 11.

Abstract

TAKEDA-143242 (TAK-242) is a small molecule shown to inhibit lipopolysaccharide-induced intracellular signaling and inflammation. In vitro studies demonstrated that TAK-242 can prevent release of TNF-α, IL-1β, and IL-6 from activated macrophages of several species, including pigs. This study tested the hypothesis that TAK-242 would protect pigs from lethal gram-negative peritonitis via an anti-cytokine mechanism. A validated model of porcine gram-negative peritonitis, which employs chronically inplantated cardiac transducers and aortic and pulmonary artery catheters, was used. Pigs were pretreated with TAK-242 or its vehicle via a blinding procedure prior to intraperitoneal implantation of an LD(90) dose of E. coli 0111:B4 in a fibrin clot. Ten pigs were treated with TAK-242 and nine with its vehicle. All ten TAK-242 treated pigs survived, while three of the nine vehicle treated pigs survived (P = 0.01 χ(2) test). Pulmonary artery pressure increased markedly in vehicle pigs, and this elevation was significantly (two-way ANOVA) obviated in TAK-242 treated group. Circulating levels of cytokines in vehicle treated pigs showed increased expression (3930 ± 1770 at 1 h, 1007 ± 400 TNF-α at 2 h; 719 ± 308 of IL-1β at 2-6 h; 33000 ± 1000 of IL-6 at 2-4 h [pg/mL, mean ± SEM]). Peak circulating levels of these cytokines were significantly reduced by pretreatment with TAK-242 (<25 pg/mL TNF-α ; <100 pg/mL IL-1β; 0-1700 pg/mL IL-6, peak values). This study found that pretreatment with TAK-242 yielded significantly positive survival benefit in a lethal sepsis model that was associated with improved cardiovascular status and suppressed cytokine release.

摘要

TAKEDA-143242(TAK-242)是一种小分子,被证明可以抑制脂多糖诱导的细胞内信号转导和炎症。体外研究表明,TAK-242 可以防止几种物种(包括猪)激活的巨噬细胞释放 TNF-α、IL-1β 和 IL-6。本研究检验了这样一个假设,即 TAK-242 通过抗细胞因子机制保护猪免受致命革兰氏阴性腹膜炎。使用了经过验证的猪革兰氏阴性腹膜炎模型,该模型采用慢性植入心脏换能器和主动脉和肺动脉导管。猪在腹膜内植入 LD(90)剂量的大肠杆菌 0111:B4 纤维蛋白凝块之前,通过盲法程序用 TAK-242 或其载体预处理。10 只猪用 TAK-242 治疗,9 只用其载体治疗。所有 10 只接受 TAK-242 治疗的猪均存活,而 9 只接受载体治疗的猪中有 3 只存活(P=0.01 χ(2)检验)。肺动脉压在载体猪中显著升高,而 TAK-242 治疗组的这种升高显著(双因素方差分析)被消除。载体治疗猪的循环细胞因子水平显示表达增加(1 小时时为 3930±1770pg/mL,2 小时时为 1007±400TNF-α;2-6 小时时为 719±308pg/mL 的 IL-1β;2-4 小时时为 33000±1000pg/mL 的 IL-6[pg/mL,均值±SEM])。用 TAK-242 预处理显著降低了这些细胞因子的循环峰值水平(<25pg/mL 的 TNF-α;<100pg/mL 的 IL-1β;0-1700pg/mL 的 IL-6,峰值)。本研究发现,在与改善心血管状态和抑制细胞因子释放相关的致死性败血症模型中,用 TAK-242 预处理可显著提高生存率,带来显著的正效益。

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