首页> 外文期刊>International immunopharmacology >DGAEE, a newly synthesized derivative of glycyrrhetinic acid, potently attenuates mouse septic shock via its main metabolite DGA in an IL-10-dependent manner
【24h】

DGAEE, a newly synthesized derivative of glycyrrhetinic acid, potently attenuates mouse septic shock via its main metabolite DGA in an IL-10-dependent manner

机译:DGAEE是一种新合成的甘草次酸衍生物,可通过其主要代谢产物DGA以IL-10依赖的方式有效减弱小鼠败血性休克。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Endotoxin can stimulate inflammatory cytokine release from monocytes/macrophages and result in septic shock. Glycyrrhetinic acid (GA), the main bioactive component of licorice, possesses substantial anti-inflammatory activity. Here, we explored effect of 11-deoxy-18 alpha-glycyrrhetinic acid-30-ethyl ester (DGAEE), a newly synthesized derivative of GA, on septic shock. DGAEE and its main metabolite 11-deoxy-18 alpha-glycyrrhetinic acid (DGA) significantly alleviated septic shock as evidenced by improvements of survival rates, lung histopathological changes and wet/dry ratio in lipopolysaccharide (LPS)/D-galactosamine-stimulated mice, and decreased blood pressure in LPS/D-galactosamine-stimulated rats. The two compounds decreased serum levels of NO, TNF-alpha, IL-6, IL-1 beta, and increased the level of IL-10 more potently in mice. In LPS-stimulated RAW 264.7 cells, DGA but not DGAEE showed marked regulation of NO, TNF-alpha, IL-6 and IL-10 levels, suggesting that DGAEE display anti-shock effect by DGA rather than itself. Moreover, the neutralizing antibody against IL-10 markedly prohibited the inhibitory effect of DGA on the production of cytokines from RAW 264.7 cells, and AS101 (an inhibitor of IL-10 biosynthesis) almost completely reversed the anti-shock effect of DGA in mice. In addition, DGA did not affect activation of NF-kappa B-p65 and p38 MAPK as well as I kappa B alpha degradation, but moderately reduced activation of ERK and JNK, and markedly increased phosphorylation of GSK3 beta in LPS-stimulated RAW 264.7 cells. LY294002 (an inhibitor of GSK3 beta phosphorylation) and LiCl (an inhibitor of GSK3 beta activity) diminished and potentiated increase of IL-10 levels by DGA, respectively. In conclusion, DGAEE alleviates septic shock through DGA in an IL-10-dependent manner, and the mechanism is related to inactivation of GSK3 beta. (C) 2015 Elsevier B.V. All rights reserved.
机译:内毒素可刺激炎性细胞因子从单核细胞/巨噬细胞释放,并导致败血性休克。甘草的主要生物活性成分甘草次酸(GA)具有重要的抗炎活性。在这里,我们探讨了GA的新合成衍生物11-脱氧-18α-甘草次酸30-乙酯(DGAEE)对败血性休克的作用。 DGAEE及其主要代谢物11-脱氧-18α-甘草次酸(DGA)可以显着减轻败血性休克,其表现为脂多糖(LPS)/ D-半乳糖胺刺激的小鼠的存活率,肺组织病理学变化和干/湿比的提高,和降低LPS / D-半乳糖胺刺激的大鼠的血压。这两种化合物在小鼠中降低了NO,TNF-α,IL-6,IL-1β的血清水平,并更有效地提高了IL-10的水平。在LPS刺激的RAW 264.7细胞中,DGA而不是DGAEE显示出NO,TNF-α,IL-6和IL-10水平的明显调节,这表明DGAEE表现出了DGA而非自身的抗休克作用。此外,针对IL-10的中和抗体明显禁止了DGA对RAW 264.7细胞产生细胞因子的抑制作用,而AS101(IL-10生物合成的抑制剂)几乎完全逆转了DGA对小鼠的抗休克作用。此外,DGA不会影响NF-κB-p65和p38 MAPK的激活以及IκBα的降解,但会适度降低ERK和JNK的激活,并显着增加LPS刺激的RAW 264.7细胞中GSK3β的磷酸化。 。 LY294002(GSK3β磷酸化的抑制剂)和LiCl(GSK3β活性的抑制剂)分别通过DGA减少和增强了IL-10水平。总之,DGAEE可以通过IL-10依赖性方式减轻DGA引起的败血性休克,其机制与GSK3 beta失活有关。 (C)2015 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号