陈海霞, 李雯, 周春骄, 力弘, 章蕴毅, 陈道峰. 柴胡多糖对空肠弯曲菌离体再刺激狼疮样小鼠脾细胞作用研究J. 药学学报, 2016,51(7): 1098-1104. doi: 10.16438/j.0513-4870.2016-0052
引用本文: 陈海霞, 李雯, 周春骄, 力弘, 章蕴毅, 陈道峰. 柴胡多糖对空肠弯曲菌离体再刺激狼疮样小鼠脾细胞作用研究J. 药学学报, 2016,51(7): 1098-1104. doi: 10.16438/j.0513-4870.2016-0052
CHEN Hai-xia, LI Wen, ZHOU Chun-jiao, LI Hong, ZHANG Yun-yi, CHEN Dao-feng. Effect of Bupleurum polysaccharides on splenocytes from lupus like mouse re-challenged with Campylobacter jejuni-S131 in vitroJ. Acta Pharmaceutica Sinica, 2016,51(7): 1098-1104. doi: 10.16438/j.0513-4870.2016-0052
Citation: CHEN Hai-xia, LI Wen, ZHOU Chun-jiao, LI Hong, ZHANG Yun-yi, CHEN Dao-feng. Effect of Bupleurum polysaccharides on splenocytes from lupus like mouse re-challenged with Campylobacter jejuni-S131 in vitroJ. Acta Pharmaceutica Sinica, 2016,51(7): 1098-1104. doi: 10.16438/j.0513-4870.2016-0052

柴胡多糖对空肠弯曲菌离体再刺激狼疮样小鼠脾细胞作用研究

Effect of Bupleurum polysaccharides on splenocytes from lupus like mouse re-challenged with Campylobacter jejuni-S131 in vitro

  • 摘要: 空肠弯曲菌(Campylobacter jejuni-S131, CJ-S131)免疫小鼠建立诱导型狼疮样模型。模型鼠脾细胞加入CJ-S131再次刺激以建立离体炎症模型,同时离体给予小叶黑柴胡多糖(Bupleurum smithii var. parvifolium polysaccharides, BPs),研究BPs防治狼疮的作用机制。BALB/c小鼠随机分为正常对照组、佐剂对照组和模型组。在Day 0和Day 14,以CJ-S131免疫小鼠建立狼疮样模型。Day 19取各组脾细胞,再分为空白组、单给药物组(BPs 5、10、20和40 μg·mL-1)、CJ-S131单刺激组和CJ-S131刺激剂联合药物处理组。ELISA法检测培养48 h上清中总免疫球蛋白G(IgG)、抗双链DNA(dsDNA)抗体、干扰素-γ(IFN-γ)、白细胞介素-10(IL-10)和IL-17的水平,MTT法测定药物对狼疮样小鼠脾细胞增殖活性的影响。结果显示,BPs显著地降低CJ-S131离体再刺激引起的总IgG、抗dsDNA抗体、IFN-γ和IL-10的高表达。BPs对高表达的IL-17水平和脾细胞活性无明显影响。研究表明,CJ-S131离体再刺激狼疮样小鼠脾细胞可建立离体炎症模型。BPs可能通过调节脾细胞分泌狼疮相关抗体和因子发挥药效。

     

    Abstract: Mice were immunized with Campylobacter jejuni-S131(CJ-S131) to establish the lupus-like model. Splenocytes from lupus like mice were challenged with CJ-S131 to induce inflammatory response in vitro. Bupleurum smithii var. parvifolium polysaccharides (BPs) was added in the inflammatory model to observe its underlying mechanisms of action on lupus. BALB/c mice were randomly divided into three groups including normal control group, adjuvant control group and lupus-like model. Mice were immunized on Day 0 and 14 with CJ-S131 to establish lupus-like syndrome, and sacrificed on Day 19. Splenocytes from each group were collected and divided into blank control group, BPs added group (BPs 5, 10, 20, 40 μg·mL-1), CJ-S131 stimulated group, and CJ-S131 plus BPs group. The levels of total IgG, anti-dsDNA antibody, interferon-γ, interleukin-10(IL-10) and IL-17 were quantified by ELISA. The proliferation of splenocytes was determined in the MTT assay. BPs significantly suppressed the high levels of total IgG, anti-dsDNA antibody, IFN-γ and IL-10 stimulated by CJ-S131 and had no significant effects on increased IL-17 secretion and splenocytes proliferation. The results suggest that re-stimulation of splenocytes with CJ-S131 could establish an inflammatory model in vitro. The effect of BPs on lupus might is related to its inhibition of the production of autoantibodies and associated cytokines.

     

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