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首页> 外文期刊>Neural regeneration research >Ramulus Cinnamomi extract attenuates neuroinflammatory responses via downregulating TLR4/MyD88 signaling pathway in BV2 cells
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Ramulus Cinnamomi extract attenuates neuroinflammatory responses via downregulating TLR4/MyD88 signaling pathway in BV2 cells

机译:兔毛肉桂提取物通过下调BV2细胞中的TLR4 / MyD88信号通路来减轻神经炎症反应

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Ramulus Cinnamomi (RC), a traditional Chinese herb, has been used to attenuate inflammatory responses. The purpose of this study was to investigate the effect of RC extract on lipopolysaccharide (LPS)-induced neuroinflammation in BV2 microglial cells and the underlying mechanisms involved. BV2 cells were incubated with normal medium (control group), LPS, LPS plus 30 μg/mL RC extract, or LPS plus 100 μg/mL RC extract. The BV2 cell morphology was observed under an optical microscope and cell viability was detected by MTT assay. Nitric oxide level in BV2 cells was detected using Griess regents, and the levels of interleukin-6, interleukin-1β, and tumor necrosis factor α in BV2 cells were determined by ELISA. The expression levels of cyclooxygenase-2, Toll-like receptor 4 and myeloid differentiation factor 88 proteins were detected by western blot assay. Compared with the LPS group, both 30 and 100 μg/mL RC extract had no significant effect on the viability of BV2 cells. The levels of nitric oxide, interleukin-6, interleukin-1β and tumor necrosis factor α in BV2 cells were all significantly increased after LPS induction, and the levels were significantly reversed after treatment with 30 and 100 μg/mL RC extract. Furthermore, RC extract significantly inhibited the protein expression levels of cyclooxygenase-2, Toll-like receptor 4 and myeloid differentiation factor 88 in LPS-induced BV2 cells. Our findings suggest that RC extract alleviates neuroinflammation by downregulating the TLR4/MyD88 signaling pathway.
机译:Ramulus Cinnamomi(RC)是一种传统中草药,已被用来减弱炎症反应。这项研究的目的是调查RC提取物对脂多糖(LPS)诱导的BV2小胶质细胞神经炎症的影响及其涉及的潜在机制。将BV2细胞与正常培养基(对照组),LPS,LPS加30μg/ mL RC提取物或LPS加100μg/ mL RC提取物孵育。在光学显微镜下观察BV2细胞形态,并通过MTT法检测细胞活力。使用Griess试剂检测BV2细胞中的一氧化氮水平,并通过ELISA测定BV2细胞中的IL-6,IL-1β和肿瘤坏死因子α的水平。 Western blot法检测环氧合酶-2,Toll样受体4和髓样分化因子88蛋白的表达水平。与LPS组相比,30和100μg/ mL RC提取物对BV2细胞的活力均无明显影响。 LPS诱导后,BV2细胞中的一氧化氮,白细胞介素-6,白细胞介素-1β和肿瘤坏死因子α的水平均显着增加,并且在用30和100μg/ mL RC提取物处理后,其水平显着逆转。此外,RC提取物显着抑制LPS诱导的BV2细胞中环氧合酶2,Toll样受体4和髓样分化因子88的蛋白表达水平。我们的发现表明RC提取物通过下调TLR4 / MyD88信号传导途径减轻神经炎症。

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