Ramulus Cinnamomi extract attenuates neuroinflammatory responses via downregulating TLR4/MyD88 signaling pathway in BV2 cells

被引:22
作者
Yang, Huan [1 ,2 ]
Cheng, Xiao [1 ,2 ]
Yang, Ying-lin [1 ,2 ]
Wang, Yue-hua [1 ,2 ,3 ]
Du, Guan-hua [1 ,2 ,3 ]
机构
[1] Chinese Acad Med Sci, Inst Mat Med, Beijing Key Lab Drug Target Identificat & Drug Sc, Beijing, Peoples R China
[2] Peking Union Med Coll, Beijing, Peoples R China
[3] Chinese Acad Med Sci, Inst Mat Med, State Key Lab Bioact Subst & Funct Nat Med, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
nerve regeneration; Ramulus Cinnamomi; BV2; cells; lipopolysaccharide; neuroinflammation; pro-inflammatory factors; TLR4/MyD88 signaling pathway; nitric oxide; interleukin-6; interleukin-1; beta; tumor necrosis factor alpha; neuronal regeneration; FACTOR-KAPPA-B; NITRIC-OXIDE; ACTIVATED MICROGLIA; EXPRESSION; RECOGNITION; RECEPTORS; INJURY; NRF2;
D O I
10.4103/1673-5374.219048
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 mu g/mL RC extract, or LPS plus 100 mu g/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-1 beta, and tumor necrosis factor a 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 mu g/mL RC extract had no significant effect on the viability of BV2 cells. The levels of nitric oxide, interleukin-6, interleukin-1 beta and tumor necrosis factor a in BV2 cells were all significantly increased after LPS induction, and the levels were significantly reversed after treatment with 30 and 100 mu g/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.
引用
收藏
页码:1860 / 1864
页数:5
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