红车轴草提取物对小鼠淋巴细胞活化与增殖及巨噬细胞分泌NO的影响(英文)  被引量:1

Effects of red clover extract on the activation and proliferation of mouse T lymphocytes and the NO secretion of mouse macrophages

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作  者:杨志[1] 黄秀艳[1] 曾耀英[1] 

机构地区:[1]暨南大学组织移植与免疫实验中心,广东广州510632

出  处:《药学学报》2008年第10期1019-1024,共6页Acta Pharmaceutica Sinica

基  金:"973"National Basic Research Program of China(2006CB504201,2004CB720100);the Key Sci-tech Development Project of Guangzhou (2006Z-E0091);Natural Foundation of Guangdong Province(2006B36030016).

摘  要:探讨红车轴草提取物(RCE)在体外对小鼠T淋巴细胞和巨噬细胞的影响。MTT法检测RCE对细胞的毒性作用。荧光抗体染色结合流式细胞术检测RCE对T淋巴细胞在Con A的刺激下表达活化抗原CD69、CD25、CD71的影响。CFDA-SE标记技术结合流式细胞术分析RCE对T淋巴细胞在Con A诱导下增殖情况的影响。Griess法检测RCE对小鼠巨噬细胞在LPS刺激24 h后分泌NO的影响。RCE对小鼠有潜在的抗炎作用。RCE对小鼠淋巴细胞和巨噬细胞的细胞毒作用很小。不同质量浓度的RCE能够很好的抑制过量的炎症相关信号分子表达,如NO,CD69,CD25,CD71,且呈剂量依赖性。RCE能够抑制T淋巴细胞的增殖。数据显示RCE可能通过对小鼠淋巴细胞活化与增殖及巨噬细胞NO分泌的抑制展示其抗炎效应。The study investigated the effects of red clover extract (RCE) on mouse T macrophages and lymphocytes in vitro. The cell toxic effect of RCE was estimated by MTT assay. Multiple-fluorescence staining plus flow cytometry were used to detect the effect of RCE on CD69/CD25/CDT1 expression of mouse T lymphocytes stimulated by Con A; CFDA-SE staining plus flow cytometry were used to analyze the effect of RCE on proliferation of T lymphocytes activated by Con A; The effect of RCE on nitric oxide (NO) secretion of mouse macrophages stimulated by lipopolysaccharide (LPS) for 24 h was assayed by Griess reagent system. We found that RCE had potent anti-inflammatory effects on mice. RCE had little cell toxic effect on mouse lymphocytes and macrophages. RCE strongly inhibited the excessive production of inflammatory mediators (NO, CD69, CD25, CD71 ), in a dose-dependent manner, like cyclosporine A injection. RCE could inhibit proliferation of CD3^+ T lymphocytes. These data suggested that RCE might exhibit anti-inflammatory effect by inhibiting the activation and proliferation of mouse lymphocytes and the NO secretion of mouse macrophages.

关 键 词:红车轴草提取物 淋巴细胞 巨噬细胞 增殖 活化 一氧化氮 

分 类 号:R392.12[医药卫生—免疫学]

 

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