首页> 外文期刊>European Journal of Pharmacology: An International Journal >A tetramethoxychalcone from Chloranthus henryi suppresses lipopolysaccharide-induced inflammatory responses in BV2 microglia
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A tetramethoxychalcone from Chloranthus henryi suppresses lipopolysaccharide-induced inflammatory responses in BV2 microglia

机译:来自Chloranthus henryi的四甲氧基查尔酮抑制BV2小胶质细胞中脂多糖诱导的炎症反应

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摘要

Neuroinflammation underlies the pathogenesis and progression of neurodegenerative diseases. 2'-hydroxy-4,3',4',6'-tetramethoxychalcone (HTMC) is a known chalcone derivative isolated from Chloranthus henryi with anti-inflammatory activities in BV2 macrophages. However, its pharmacological effects on microglial cells have not been demonstrated. To this end, we examined the effects of HTMC on lipopolysaccharide (LPS)-induced inflammatory responses in BV2 microglial cells. HTMC concentration-dependently inhibited LPS-induced expression of inflammatory enzymes including inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), nitric oxide (NO) production, and the secretion of inflammatory cytokines, including tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, and IL-6. In addition, HTMC inhibited reactive oxygen species (ROS) production by reducing NADPH oxidase (Nox) 2 and Nox4 expression. In addition, HTMC interfered LPS-induced c-Jun N-terminal kinase 1/2 (JNK) phosphorylation in a time-and concentration-dependent manner. By inhibiting phosphorylation and nuclear translocation of Jun, HTMC suppressed LPS-induced activator protein-1 (AP-1) activation. Taken together, our data indicate that HTMC suppresses inflammatory responses in LPS-stimulated BV2 microglial cells by modulating JNK-AP-1 and NADPH oxidases-ROS pathways. HTMC represents a promising therapeutic agent for neurodegenerative and related aging-associated diseases. (C) 2016 Elsevier B.V. All rights reserved.
机译:神经炎症是神经退行性疾病的发病机理和进展的基础。 2'-羟基-4,3',4',6'-四甲氧基查尔酮(HTMC)是一种已知的查尔酮衍生物,从Chloranthus henryi中分离出来,对BV2巨噬细胞具有抗炎活性。但是,尚未证明其对小胶质细胞的药理作用。为此,我们检查了HTMC对BV2小胶质细胞中脂多糖(LPS)诱导的炎症反应的影响。 HTMC浓度依赖性地抑制LPS诱导的炎症酶的表达,包括诱导型一氧化氮合酶(iNOS)和环氧合酶2(COX-2),一氧化氮(NO)的产生,以及炎症细胞因子的分泌,包括肿瘤坏死因子(TNF) ),白介素(IL)-1和IL-6。此外,HTMC通过减少NADPH氧化酶(Nox)2和Nox4表达来抑制活性氧(ROS)的产生。此外,HTMC以时间和浓度依赖性方式干扰LPS诱导的c-Jun N末端激酶1/2(JNK)磷酸化。通过抑制Jun的磷酸化和核易位,HTMC抑制LPS诱导的激活蛋白1(AP-1)激活。两者合计,我们的数据表明HTMC通过调节JNK-AP-1和NADPH氧化酶-ROS途径抑制LPS刺激的BV2小胶质细胞的炎症反应。 HTMC代表了一种用于神经退行性疾病和相关的衰老相关疾病的有前途的治疗剂。 (C)2016 Elsevier B.V.保留所有权利。

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