通过阻断白细胞介素-1β和白细胞介素-6的产生介导萜类化合物对脂多糖诱导的内毒素血症的保护作用

Yeo Dae Yoon, Myeong Youl Lee, Byeong Jo Choi, Chang Woo Lee, Hyunju Lee, Joo-Hee Kwon, Jeong-Wook Yang, Jong Soon Kang
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引用次数: 2

摘要

Terrein是一种真菌代谢物,具有抗黑色素生成、抗癌和抗菌活性。然而,其在内毒素血症中的作用至今尚未被研究。在本研究中,我们研究了terrein对小鼠脂多糖(LPS)诱导的内毒素血症的影响,并表征了其潜在的作用机制。在lps诱导的内毒素血症模型中,用terrein治疗可以提高小鼠的存活率,减少炎症细胞因子的产生,包括白细胞介素-1β (IL-1β)和白细胞介素-6 (IL-6)。此外,terrein抑制lps诱导的小鼠巨噬细胞样细胞系RAW 264.7细胞IL-1β和IL-6的产生,并且在lps刺激的RAW 264.7细胞中,terrein也抑制IL-1β和IL-6的mRNA表达。进一步的研究表明,terrein阻断了lps诱导的核因子(NF)/κB p65亚基的磷酸化,并抑制了c-Jun n-末端激酶(JNK)和p38丝裂原活化蛋白激酶(MAPK)的磷酸化。综上所述,这些结果表明,terrein通过阻断炎症细胞因子的产生,在lps诱导的小鼠内毒素血症中再次发挥保护作用。我们的研究结果还表明,terrein的抗炎作用可能是通过阻断NF-κB、JNK和p38 MAPK信号通路的激活来介导的,至少部分是这样。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Protection against Lipopolysaccharide-Induced Endotoxemia by Terrein Is Mediated by Blocking Interleukin-1β and Interleukin-6 Production.

Protection against Lipopolysaccharide-Induced Endotoxemia by Terrein Is Mediated by Blocking Interleukin-1β and Interleukin-6 Production.

Protection against Lipopolysaccharide-Induced Endotoxemia by Terrein Is Mediated by Blocking Interleukin-1β and Interleukin-6 Production.

Protection against Lipopolysaccharide-Induced Endotoxemia by Terrein Is Mediated by Blocking Interleukin-1β and Interleukin-6 Production.

Terrein is a fungal metabolite and has been known to exert anti-melanogenesis, anti-cancer, and anti-bacterial activities. However, its role in endotoxemia has never been investigated until now. In the present study, we examined the effect of terrein on lipopolysaccharide (LPS)-induced endotoxemia in mice and characterized the potential mechanisms of action. Treatment with terrein increased the survival of mice and decreased the production of inflammatory cytokines, including interleukin-1β (IL-1β) and interleukin-6 (IL-6) in an LPS-induced endotoxemia model. In addition, terrein suppressed the LPS-induced production of IL-1β and IL-6 in RAW 264.7 cells, a murine macrophage-like cell line, and the mRNA expression of IL-1β and IL-6 was also inhibited by terrein in LPS-stimulated RAW 264.7 cells. Further study demonstrated that terrein blocked LPS-induced phosphorylation of p65 subunit of nuclear factor (NF)/κB and the phosphorylation of c-Jun N-terminal kinase (JNK) and p38 mitogen-activated protein kinase (MAPK) was also suppressed by terrein treatment. Collectively, these results suggest that terrein exerts a protective effect again LPS-induced endotoxemia in mice by blocking the production of inflammatory cytokines. Our results also suggest that the anti-inflammatory effect of terrein might be mediated, at least in part, by blocking the activation of NF-κB, JNK, and p38 MAPK signaling pathways.

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