4.6 Article

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

Journal

NEURAL REGENERATION RESEARCH
Volume 12, Issue 11, Pages 1860-1864

Publisher

WOLTERS KLUWER MEDKNOW PUBLICATIONS
DOI: 10.4103/1673-5374.219048

Keywords

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

Funding

  1. National Natural Science Foundation of China [81473383]
  2. Medical and Health Innovation Project of Chinese Academy of Medical Sciences [2016-I2M-3-007]
  3. Key Project of New-Drugs Creation of Science and Technology of China [2012ZX09103101-078, 2017ZX09101003-003-019]

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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 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.

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