Inhibitory effects of dihydroartemisinin on LPS-induced inflammatory response in BV-2 microglial cells
Basic Medicine|更新时间:2026-01-09
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Inhibitory effects of dihydroartemisinin on LPS-induced inflammatory response in BV-2 microglial cells
Journal of Third Military Medical UniversityVol. 39, Issue 22, Pages: 2189-2194(2017)
作者机构:
1.400016 重庆,重庆医科大学神经科学研究中心
2.400038 重庆,第三军医大学西南医院疼痛科
作者简介:
基金信息:
the General Program of National Natural Science Foundation of China(81371221);the Project of Basic and Frontier Research of Chongqing(CSTC2016jcyjA0069);the Project of Scientific and Technological Research of Chongqing Municipal Education Commission(KJ130317);the Science and Technology Project of Yuzhong District, Chongqing(20130132)
Wanxiang QIN, Min LUO, Ying SHI, et al. Inhibitory effects of dihydroartemisinin on LPS-induced inflammatory response in BV-2 microglial cells[J]. Journal of Third Military Medical University, 2017, 39(22): 2189-2194.
DOI:
Wanxiang QIN, Min LUO, Ying SHI, et al. Inhibitory effects of dihydroartemisinin on LPS-induced inflammatory response in BV-2 microglial cells[J]. Journal of Third Military Medical University, 2017, 39(22): 2189-2194. DOI: 10.16016/j.1000-5404.201706124.
Inhibitory effects of dihydroartemisinin on LPS-induced inflammatory response in BV-2 microglial cells
To investigate the inhibitory effect of dihydroartemisinin (DHA) on lipopolysaccharide (LPS)-induced inflammatory response in BV-2 microglial cells.
Methods
2
Inflammatory model was established by exposure of BV-2 cells to LPS for 24 h. Then after the cells were treated with different concentrations of DHA (0.5
1
2 and 4 μmol/L)
cell viability was tested with CCK-8 assay. The cell morphology was observed under inverted phase contrast microscope after the inflammatory cell model under the treatment of a harmless concentration (1 μmol/L) of DHA
The mRNA expression of iNOS
IL-1β
IL-6 and TNF-α was measured by RT-PCR. The contents of TNF-α
IL-1β and IL-6 in the supernatant were detected by ELISA. The expression of the nuclear NF-κB (p65)
IκBα
and TLR4 were analyzed by Western blotting.
Results
2
DHA showed no significant effect on cell viability when the concentration was lower than 2 μmol/L (
P
>
0.05). DHA inhibited the cell morphological changes induced by LPS. DHA treatment resulted in the decreases in the mRNA expression levels of iNOS
IL-1β
IL-6 and TNF-α (
P
<
0.01)
the production of pro-inflammatory cytokines IL-1β
IL-6
TNF-α
the protein levels of TLR4
intracytoplasmic IκBα and the nuclear translocation of NF-κB p65 (
P
<
0.01).
Conclusion
2
DHA inhibits the inflammatory responses
activation of NF-κB of BV-2 microglial cells induced by LPS
and thus suppresses the production of pro-inflammatory cytokines
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