• EI
  • Scopus
  • 食品科学与工程领域高质量科技期刊分级目录第一方阵T1
  • DOAJ
  • EBSCO
  • 北大核心期刊
  • 中国核心学术期刊RCCSE
  • JST China
  • FSTA
  • 中国精品科技期刊
  • 中国农业核心期刊
  • CA
  • WJCI
  • 中国科技核心期刊CSTPCD
  • 中国生物医学SinoMed
中国精品科技期刊2020
李木霞, 苏冀彦, 李丹, 林吉, 谢意珍, 李运容. 牛樟芝醇提物体外抗炎活性研究[J]. 食品工业科技, 2019, 40(11): 161-167. DOI: 10.13386/j.issn1002-0306.2019.11.027
引用本文: 李木霞, 苏冀彦, 李丹, 林吉, 谢意珍, 李运容. 牛樟芝醇提物体外抗炎活性研究[J]. 食品工业科技, 2019, 40(11): 161-167. DOI: 10.13386/j.issn1002-0306.2019.11.027
LI Mu-xia, SU Ji-yan, LI Dan, LIN Ji, XIE Yi-zhen, LI Yun-rong. Anti-inflammatory Effects of Antrodia cinnamomea Ethanol Extract in Vitro[J]. Science and Technology of Food Industry, 2019, 40(11): 161-167. DOI: 10.13386/j.issn1002-0306.2019.11.027
Citation: LI Mu-xia, SU Ji-yan, LI Dan, LIN Ji, XIE Yi-zhen, LI Yun-rong. Anti-inflammatory Effects of Antrodia cinnamomea Ethanol Extract in Vitro[J]. Science and Technology of Food Industry, 2019, 40(11): 161-167. DOI: 10.13386/j.issn1002-0306.2019.11.027

牛樟芝醇提物体外抗炎活性研究

Anti-inflammatory Effects of Antrodia cinnamomea Ethanol Extract in Vitro

  • 摘要: 目的:研究牛樟芝醇提物(Ethanol extract from Antrodia cinnamomea ,AC-E)对T细胞及T细胞亚群的影响,探讨牛樟芝的抗炎作用。方法:使用为3 μg/mL刀豆蛋白A(Concanavalin A,ConA)刺激BALB/c小鼠脾淋巴细胞建立体外模型,以不同浓度AC-E(12.5、25.0、50.0 μg/mL)干预72 h。以3-(4,5-二甲基噻唑-2-基)-5-(3-羧甲酯基)-2-(4-磺苯基)-2H-四唑(MTS)试剂检测细胞活力;应用流式细胞术(Flowcytometry,FCM)分析其凋亡情况和T细胞及其亚群的比例变化情况;以酶联免疫吸附测定法(Enzyme linked immunosorbent assay,ELISA)分析培养上清液中γ-干扰素(Interferon-γ,IFN-γ)、肿瘤坏死因子-α(Tumor nerosis factor-α,TNF-α)的分泌情况。结果:MTS检测表明,高剂量AC-E可明显抑制ConA诱导的淋巴细胞增殖;流式细胞术结果表明,中高剂量组AC-E可明显诱导被刺激后的细胞发生凋亡,AC-E能使增殖的T细胞及T细胞亚群凋亡;ELISA检测结果表明,AC-E能抑制促炎因子TNF-α、IFN-γ的分泌,给药组的细胞因子浓度接近于正常组。结论:AC-E可通过使激活增殖的T细胞凋亡进而使机体的免疫系统趋于平衡,为牛樟芝抗炎的食药用价值及深入开发提供理论依据。

     

    Abstract: Objective:To investigate the anti-inflammtory effects of ethanol extract from Antrodia cinnamomea(AC-E)on the T cell and T cell subsets,exploring the anti-inflammatory effect of Antrodia cinnamomea. Methods:Splenocytes from BAL B/C mice were treated with AC-E(12.5,25,50 μg/mL)under the stimulation by ConA(3 μg/mL)for 72 h. Cell vitality was measured by MTS assay. Apoptosis was determined with flowcytometry(FCM),as well as T cells and subsets. Concentrations of interferon-γ(IFN-γ)and tumor nerosis factor-α(TNF-α)in the supernatant were determined by enzyme linked immunosorbent assay(ELISA). Results:Data showed that the AC-E(50 μg/mL)could directly inhibit the proliferation of splenocytes under ConA stimulation. The cells in AC-E(25,50 μg/mL)dose groups showed obvious apoptosis. Results of ELISA showed that AC-E could suppress the secretions of TNF-α and IFN-γ,and the concentration of cytokines in the drug-treatment groups were close to that of normal group. Conclusion:AC-E could restore the immune system via apoptosis inducion in activated T cells,providing experimental basis and theoretical basis for anti-inflammatory application of Antrodia cinnamomea.

     

/

返回文章
返回