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金钗石斛生物总碱对脂多糖激活星形胶质细胞产生炎症因子的影响

Effects of Dendrobium nobile total alkaloids on lipopolysaccharide-induced astrocyte activation and pro-inflammatory factors production

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【作者】 张俊青吴芹龚其海张锋金凤聂晶石京山

【Author】 ZHANG Jun-qing1,2,WU Qin1,GONG Qi-hai1,ZHANG Feng1, JIN Feng1,NIE Jing1,SHI Jing-shan1(1.Dept of Pharmacology and Key Lab of Basic Pharmacology of Guizhou,Zunyi Medical College,Zunyi Guizhou 563000,China;2.Mental Hospital of Jining City,Jining Shandong 272051,China)

【机构】 遵义医学院药理学教研室贵州基础药理重点实验室济宁市精神病防治院

【摘要】 目的观察金钗石斛生物总碱对外源性内毒素脂多糖(lipopolysaccharide,LPS)激活大鼠大脑皮层星形胶质细胞(astrocyte)及诱导其产生和释放炎症介质的影响,探讨石斛生物总碱对星形胶质细胞的抗炎作用。方法通过MTS检测细胞存活率,ELISA法检测TNF-α炎性因子蛋白的表达,实时定量多聚酶链反应(real time RT-PCR)检测炎症相关基因TNF-α、IL-6 mRNA的表达。结果①LPS刺激星形胶质细胞后,MTS检测吸光度明显升高,与正常组比较差异有显著性;②金钗石斛生物总碱能够降低LPS所致的TNF-α蛋白的高表达(P<0.05);③金钗石斛生物总碱能够降低LPS诱导的星形胶质细胞吸光度的升高,同时明显抑制LPS所致的TNF-α、IL-6 mRNA的高表达。结论金钗石斛生物总碱能够拮抗LPS所引起的炎症反应,其作用与抑制星形胶质细胞的激活及其炎症因子的释放密切相关。

【Abstract】 Aim To investigate the effects of Dendrobium nobile total alkaloids on lipopolysaccharide(LPS)-induced activation of astrocytes and the subsequent release of pro-inflammatory factors.Methods The cell viability was tested by the MTS assay.The generation and release of TNF-α from astrocytes were evaluated via the enzyme link immunosorbent assay(ELISA).The mRNA expressions of TNF-α,IL-6 in astrocytes were detected by real-time RT-PCR.Results①LPS activated astrocytes resulting in significantly elevated absorbance was tested by the MTS;②Dendrobium nobile total alkaloids inhibited the LPS-induced over expressions of TNF-αprotein(compared with control group P<0.05);③Compared with the LPS group,Dendrobium nobile total alkaloids significantly inhibited LPS-induced activation of astrocytes and decreased LPS-induced mRNA overexpressions of TNF-αand IL-6.Conclusion Dendrobium nobile total alkaloids can protect against LPS-induced neuroinflammation.This neuroprotection is partly due to the inhibition of astrocyte activation and the reduced production of pro-in-flammatory factors.

【基金】 国家自然科学基金资助项目(No30960447);贵州省科技厅重点项目(No2007C-343)
  • 【文献出处】 中国药理学通报 ,Chinese Pharmacological Bulletin , 编辑部邮箱 ,2011年06期
  • 【分类号】R285
  • 【被引频次】52
  • 【下载频次】658
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