机构地区:[1]锦州医学院药理教研室,辽宁省锦州市121001 [2]锦州市药业集团器化玻有限公司,辽宁省锦州市121001 [3]锦州医学院解剖教研室,辽宁省锦州市121001
出 处:《中国临床康复》2005年第29期134-136,i0001,共4页Chinese Journal of Clinical Rehabilitation
基 金:辽宁省自然科学基金(2040987)~~
摘 要:目的:观察中药当归提取的主要活性成分阿魏酸钠对淀粉样β蛋白激活的小鼠腹腔巨噬细胞α肿瘤坏死因子、诱导型一氧化氮合酶和一氧化氮水平的影响。方法:实验于2004-03/10在锦州医学院药理实验室和解剖实验室完成。选择8~10周龄的小鼠36只,随机分为6组,每组6只。正常对照组:巨噬细胞接种24h后用培养基继续培养。淀粉样β蛋白组:巨噬细胞接种24h后在培养基中加入经老化处理的终浓度为10μmol/L的淀粉样β蛋白。淀粉样β蛋白+10,100,500μmol/L,1mmol/L阿魏酸钠组:在加入淀粉样β蛋白的同时加入10,100,500μmol/L,1mmol/L的阿魏酸钠共同孵育。培养48h后采用酶联免疫吸附法、免疫组织化学方法和Griess反应分别检测肿瘤坏死因子α分泌量、诱导型一氧化氮合酶表达和一氧化氮的生成量。结果:36只小鼠均进入结果分析。①巨噬细胞的肿瘤坏死因子α分泌量:淀粉样β蛋白组明显高于正常对照组[(281.54±14.85),(17.55±4.84)ng/L,(P<0.01)]。淀粉样β蛋白+10,100,500μmol/L,1mmol/L阿魏酸钠组可以不同程度地减少由淀粉样β蛋白诱导产生的肿瘤坏死因子α的分泌量[(238.05±6.21),(186.90±7.44),(117.55±8.08),(71.77±10.50)ng/L,P<0.01],且有明显剂量依赖关系(P<0.05)。②巨噬细胞的一氧化氮生成量:淀粉样β蛋白组明显高于正常对照组[(85.04±6.16),(26.10±3.25)μmol/L,(P<0.01)],淀粉样β蛋白+10,100,500μmol/L,1mmol/L阿魏酸钠组可以不同程度地减少由淀粉样β蛋白诱导产生的一氧化氮的量[(69.80±4.96),(54.52±3.45),(43.88±4.04),(33.83±3.13)μmol/L,P<0.01],且有明显剂量依赖关系(P<0.05)。③诱导型一氧化氮合酶的表达:正常对照组只有零星细胞染色阳性;而淀粉样β蛋白组多数细胞胞浆被染成黄褐色。各剂量组的阿魏酸钠可以不同程度地抑制由淀粉样β蛋白激活巨噬细胞造成的诱导型一氧化氮合酶的表达,该抑制作用呈明显剂量依赖性�AIM: To observe the effect of sodium ferulate, the main activity component extracted from Chinese angelica the traditional Chinese medicine, on the level of the tumor necrosis factor alpha (TNF-α), induction nitricoxide synthase (iNOS) and nitrogen monoxide (NO) of abdominal cavity histocyte activated by amyloid beta protein in rats. METHODS: The experiment was completed in cooperation of the Department of Pharmacology and Department of Anatomy of Jinzhou Medical College from March to October 2004. Thirty-six mice aged from 8 to 10 weeks were selected and divided randomly into 6 groups with 6 in each group. Normal control group: Twenty-four hours after inoculation macrophages were cultured continuously by medium. Amyloid beta protein group: Twenty-four hours after inoculation macrophages were added in arnyloid beta protein with the 10μmol/L final concentration which was conducted ageing disposal in medium. The amyloid beta protein ±10, 100, 500μmol/L, 1 mmol/L sodium ferulate group: Sodium ferulate 10,100,500μmol/L, 1 mmol/L were added at the same time of adding amyloid beta protein to incubate together. The excretion of TNF-α, and the expression of iNOS and production of NO were detected by enzyme-linked immuno-sorbent assay, irnmuneohistochemistry technique and Greiss reaction respectively 48 hours after culture. RESULTS: Thirty-six mice were all involved in the result analysis. ① The excretion of TNF-α of histocyte: It was significantly higher in amyloid beta protein group than that in normal control group [(281.54±14.85), (17.55±4.84) ng /L, (P 〈 0.01)]. The excretion of TNF-α induced by amyloid beta protein could decreased in different degree in amyloid beta protein +10, 100, 500 μmol/L, lmmol/L sodium ferulate group [(238.05±6.21), (186.90±7.44), (117.55±8.08), (71.77±10.50)ng/L, P 〈 0.01] and had significant dosage dependence relation (P 〈 0.05).② The production of NO of histocyte: It was significantly higher in amyloid
分 类 号:R741[医药卫生—神经病学与精神病学]
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