Ginsenoside Rg1 regulating BV2 microglia polarization in lipopolysaccharide-induced inflammatory response via peroxisome proliferator activated receptor γ

LI Ting-yu WANG Xing-hang CHI Xiao-chen LI Kun-fang BAO Cui-fen

Acta Anatomica Sinica ›› 2023, Vol. 54 ›› Issue (3) : 269-275.

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Acta Anatomica Sinica ›› 2023, Vol. 54 ›› Issue (3) : 269-275. DOI: 10.16098/j.issn.0529-1356.2023.03.003
Neurobiology

Ginsenoside Rg1 regulating BV2 microglia polarization in lipopolysaccharide-induced inflammatory response via peroxisome proliferator activated receptor γ

  • LI  Ting-yu1  WANG  Xing-hang1 CHI  Xiao-chen1 LI  Kun-fang BAO  Cui-fen2*#br#
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Abstract

Objective To establish an inflammation model by stimulating BV2 microglia by lipopolysaccharide, and to explore the regulation effect of ginsenoside Rg1 on inflammation by activating peroxisome proliferator activated receptor γ(PPARγ) receptor protein.  Methods BV2 microglia were randomly divided into control group, model group, ginsenoside Rg1 group, rosiglitazone group and GW9662 group. The control group did not do any treatment, the model group was treated with 1 mg/L lipopolysaccharide, and the other groups were treated with lipopolysaccharide added with 0.4mmol/L ginsenoside Rg1, 10 μmol/L rosiglitazone or 10 μmol/L respectively. GW9662. The proliferation of BV2 microglia in each group was detected by CCK-8 method; PPAR-γ, phospho-NF-κB p65 (p-NF-κB p65), induced expression of inducible nitric oxide synthase(iNOS) and human arginase 1(ARG-1) proteins. ELISA was used to detect the inflammatory factors interleukin-1β(IL-1β), interleukin-6(IL-6), interleukin-8(IL-8) and the content of tumor necrosis factor-α (TNF-α).   Results Compared with the control group, the cell proliferation rate in the model group was significantly increased, and the contents of IL-1β, IL-6, IL-8 and TNF-α increased significantly. The results of immunofluorescence and Western blotting showed that iNOS and p-NF-κB p65 increased significantly, and the positive expressions of PPARγ and ARG-1 decreased significantly(both P<0.01). The expression level of TNF-α decreased, the positive expressions of iNOS and p-NF-κB p65 decreased significantly, and the positive expressions of PPARγ and ARG-1 increased significantly(all P<0.01).   Conclusion Ginsenoside Rg1 inhibits the inflammatory response of BV2 microglia after lipopolysaccharide stimulation, and its mechanism may be related to the regulation of PPARγ/NF-κB pathway to promote the M2-type polarization of microglia.

Key words

Ginsenoside Rg1 / Peroxisome proliferator activated receptor γ / BV2 cell / Polarization / Western blotting 

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LI Ting-yu WANG Xing-hang CHI Xiao-chen LI Kun-fang BAO Cui-fen.
Ginsenoside Rg1 regulating BV2 microglia polarization in lipopolysaccharide-induced inflammatory response via peroxisome proliferator activated receptor γ
[J]. Acta Anatomica Sinica. 2023, 54(3): 269-275 https://doi.org/10.16098/j.issn.0529-1356.2023.03.003

References

[1]Voet  S, Prinz M, van Loo G. Microglia in central nervous system inflammation and multiple sclerosis pathology[J].Trends Mol Med, 2019,25(2):112-123.
[2]Xu  HB, Luo Y.Myeloid cell-activated receptor 2 regulates the M2-type polarization of microglia in a mouse model of oxygen and glucose deprivation/reoxygenation[J].Acta Anatomica Sinica,2021,52(3):329-336. (in Chinese)
胥虹贝,罗勇.髓样细胞激活受体2调控氧糖剥夺/复氧模型小鼠小胶质细胞向M2型极化[J].解剖学报,2021,52(3):329-336.
[3]Tang  Y, Le W. Differential roles of M1 and M2 microglia in neurodegenerative diseases[J]. Mol Neurobiol,2016,53(2):1181-1194.
[4]Liao  S, Bai Y, Zheng X. A novel compound DBZ ameliorates neuroinflammation in LPS-stimulated microglia and ischemic stroke rats: role of Akt(Ser473)/GSK3β(Ser9)-mediated Nrf2 activation[J].Redox Biol,2020,36:101644.
[5]Gao J, Su G,Liu J,et al. Mechanisms of inhibition of excessive microglial activation by melatonin[J]. J Mol Neurosci, 2020, 70(8):1229-1236.
[6]Vetuschi  A, Pompili S,Sferra R. PPAR-γ with its anti-inflammatory and anti-fibrotic action could be an effective therapeutic target in IBD[J].Eur Rev Med Pharmacol Sci,2018,22(24):8839-8848.
[7]Villapol  S. Roles of peroxisome proliferator-activated receptor gamma on brain and peripheral inflammation[J]. Cell Mol Neurobiol,2018,38(1):121-132.
[8]Wang  XH. Ginsenoside Rg1 attenuates the inflammatory response of microglia after oxygen and glucose deprivation/resupply by inhibiting the NLRP3 inflammasome pathway[D].Jinzhou: Jinzhou Medical University,2021. (in Chinese)
王兴航. 人参皂苷Rg1通过抑制NLRP3炎症小体途径减轻氧糖剥夺/复供后小胶质细胞炎症反应[D].锦州:锦州医科大学,2021.
[9]You  WD. The effect of PPAR-γ receptor-mediated microglia polarization to M2 subtype on prognosis of traumatic brain injury[D].Hangzhou: Zhejiang University,2019.  (in Chinese)
游文栋. PPAR-γ受体介导的小胶质细胞向M2亚型极化对颅脑创伤预后的影响[D].杭州:浙江大学,2019.
[10]Ji J, Xue TF, Guo XD,et al. Antagonizing peroxisome proliferator-activated receptor γ facilitates M1-to-M2 shift of microglia by enhancing autophagy via the LKB1-AMPK signaling pathway[J].Aging Cell,2018,17(4):e12774.
[11]Thurgur  H, Pinteaux E. Microglia in the neurovascular unit: blood-brain barrier-microglia interactions after central nervous system disorders[J].Neuroscience,2019,405:55-67.
[12]Luo  M, Yan D, Sun Q,et al. Ginsenoside Rg1 attenuates cardiomyocyte apoptosis and inflammation via the TLR4/NF-kB/NLRP3 pathway[J].Cell Biochem,2020,121(4):2994-3004.
[13]Bao  Y, Zhu Y, He G,et al. Dexmedetomidine attenuates neuroinflammation in LPS-stimulated BV2 microglia cells through upregulation of miR-340[J].Drug Des Devel Ther,2019,13:3465-3475.
[14]Yao  YY, Ai QL, Chen YL, et al. Ginsenoside Rg1 inhibits the proliferation of BV-2 microglia induced by lipopolysaccharide[J].Acta Anatomica Sinica,2016,47(5):614-619.  (in Chinese)
姚玥伊,艾青龙,陈媛丽,等.人参皂苷Rg1抑制脂多糖诱导BV-2小胶质细胞增殖[J].解剖学报,2016,47(5):614-619.
[15]Butturini  E, Boriero D, Mariotto S. STAT1 drives M1 microglia activation and neuroinflammation under hypoxia[J]. Arch Biochem Biophys,2019,669:22-30.
[16]Xie L, Zhang N, Zhang Q,et al. Inflammatory factors and amyloid β-induced microglial polarization promote inflammatory crosstalk with astrocytes[J].Aging (Albany NY),2020,12(22):22538-22549.
[17]Zhou  D, Ji L, Chen Y. TSPO modulates IL-4-induced microglia/macrophage M2 polarization via PPAR-γ pathway[J].Mol Neurosci,2020,70(4):542-549.
[18]Han  Q, Yuan Q, Meng X, et al. 6-Shogaol attenuates LPS-induced inflammation in BV2 microglia cells by activating PPAR-γ[J].Oncotarget,2017,8(26):42001-42006.
[19]He  Y, Gao Y, Zhang Q,et al. IL-4 switches microglia/macrophage M1/M2 polarization and alleviates neurological damage by modulating the JAK1/STAT6 pathway following ICH[J].Neuroscience,2020,437:161-171.
[20]Li  T, Wu YN, Wang H,et al. Dapk1 improves inflammation, oxidative stress and autophagy in LPS-induced acute lung injury via p38MAPK/NF-κB signaling pathway[J].Mol Immunol,2020,120:13-22.
[21]Ren  X, Chen C, Luo Y,et al. IncRNA-PLACT1 sustains activation of NF-κB pathway through a positive feedback loop with IκBα/E2F1 axis in pancreatic cancer[J].Mol Cancer,2020,19(1):35.
[22]Kim  HJ, Joe HI, Zhang Z,et al. Anti-inflammatory effect of Acalypha australis L. via suppression of NF-κB signaling in LPS-stimulated RAW 264.7 macrophages and LPS-induced septic mice[J].Mol Immunol,2020,119:123-131.
Ginsenoside Rg1 regulating BV2 microglia polarization in lipopolysaccharide-induced inflammatory response via peroxisome proliferator activated receptor γ
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