癌变·畸变·突变 ›› 2016, Vol. 28 ›› Issue (3): 214-217.doi: 10.3969/j.issn.1004-616x.2016.03.011

• 论著 • 上一篇    下一篇

原花青素对脂多糖诱导BV2小胶质细胞炎症介质分泌的影响

陈金枝1,2, 张小强1,2, 曲志华1,2, 周亚盼1,2, 张妍1,2, 梁晓瑜1,2   

  1. 1. 东南大学公共卫生学院, 江苏 南京 210009;
    2. 东南大学环境医学工程教育部重点实验室, 江苏 南京 210009
  • 收稿日期:2015-12-29 修回日期:2016-03-11 出版日期:2016-05-31 发布日期:2016-05-31
  • 通讯作者: 张小强,E-mail:zhangxq7843@126.com E-mail:zhangxq7843@126.com
  • 作者简介:陈金枝,E-mail:chenjinzhi1990@sina.com。
  • 基金资助:
    中央高校基本科研业务费专项资金资助和江苏省普通高校研究生科研创新计划资助项目资助(SJZZ_0032);江苏省卫生厅预防医学科研基金(Y2013070)

Anti-inflammatory effects of proanthocyanidin on activation of BV2 microglia by lipopolysaccharide

CHEN Jinzhi1,2, ZHANG Xiaoqiang1,2, QU Zhihua1,2, ZHOU Yapan1,2, ZHANG Yan1,2, LIANG Xiaoyu1,2   

  1. 1. School of Public Health, Southeast University, Nanjing 210009;
    2. Key Laboratory of Environmental Medicine Engineering of Ministry of Education, Southeast University, Nanjing 210009, Jiangsu, China
  • Received:2015-12-29 Revised:2016-03-11 Online:2016-05-31 Published:2016-05-31

摘要: 目的:探讨原花青素对脂多糖(LPS)激活小鼠小胶质细胞(BV2)炎症介质分泌的影响。方法:以LPS激活BV2细胞构建神经炎症模型。分别采用0.1、0.5、1.0、5.0 μg/mL原花青素预处理后,1.0 μg/mL的LPS刺激BV2细胞24 h。采用MTT法检测细胞存活率;Griess法检测BV2细胞培养液上清中一氧化氮(NO)水平;ELISA法检测肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)的分泌水平。结果:在实验剂量范围内,原花青素及LPS对BV2细胞活性均无显著影响(P>0.05)。但1.0 μg/mL LPS可引起BV2细胞各炎症因子NO、TNF-α、IL-1β和IL-6水平明显升高(P<0.05)。与LPS组相比,原花青素(0.1、0.5、1.0、5.0 μg/mL)预处理能使激活的BV2细胞培养液上清中NO释放量减少(P<0.05),TNF-α、IL-1β和IL-6含量降低(P<0.05),抑制作用呈剂量-效应关系。结论:在体外实验中,原花青素对LPS诱导小胶质细胞所致的炎症反应具有保护作用。

关键词: 原花青素, BV2细胞, 脂多糖, 神经炎症

Abstract: OBJECTIVE:To investigate the effects of pro-anthocyanidin on inhibiting inflammatory mediator secretion in LPS activation of BV2 microglia. METHODS:Neuroinflammation model was established by LPS-activated BV2 microglia.BV2 microglial were pretreated with different concentrations of pro-anthocyanidin (0.1, 0.5, 1.0, 5.0 μg/mL) and stimulated with LPS (1.0 μg/mL) for 24 h. Cell viability was assessed by MTT assay. Griess method was utilized to detect the content of NO. The secretion level of pro-inflammatory cytokines TNF-alpha, IL-1beta and IL-6 was examined using specific ELISA kits. RESULTS:Within a certain dosage ranges of pro-anthocyanidin and LPS, there was no negative effect on cell viability (P>0.05). LPS (1.0 μg/mL) significantly increased the release of inflammatory mediator nitric oxide (NO) as well as the cytokines TNF-α, IL-1β and IL-6(P<0.05). Compared with the LPS group, different concentrations of pro-anthocyanidin (0.1, 0.5, 1.0, 5.0 μg/mL) attenuated the release of NO, TNF-α, IL-1β and IL-6 in cells that were cultured in conditioned media from LPS-induced BV2 microglia. The effect was dose-dependent (P<0.05). CONCLUSION:We showed that pro-anthocyanidin has a protective effect on inflammatory responses of LPS-activated BV2 microglia in vitro.

Key words: proanthocyanidin, BV2 microglia, lipopolysaccharide, neuroinflammation

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