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机构地区:[1]潍坊医学院药理学教研室应用药理学实验室,山东潍坊261053
出 处:《中国老年学杂志》2016年第7期1540-1541,共2页Chinese Journal of Gerontology
基 金:国家自然科学基金专项基金项目(81341137);潍坊市科技局项目(201301071)
摘 要:目的探讨1,8-桉油素预处理对Aβ(25 ~ 35)诱导原代培养大鼠皮层神经元炎症反应的影响。方法原代培养大鼠皮层神经元,随机分组。采用噻唑蓝(MTT)还原反应观察神经元损伤;以Aβ(25 ~ 35)处理24 h诱导神经元损伤;酶联免疫吸附法(ELISA)检测上清液中肿瘤坏死因子(TNF)-α、白介素(IL)-1β及半胱氨酰白三烯(Cys LTs)释放水平。结果 20μmol/L的Aβ(25 ~ 35)处理神经元细胞24 h可显著降低神经元活性,增加TNF-α、IL-1β及Cys LTs的释放,1,8-桉油素10μmol/L预处理后可明显抑制Aβ(25 ~ 35)引起的细胞毒性效应,并抑制上述炎症因子及Cys LTs的释放。结论 1,8-桉油素对Aβ(25 ~ 35)诱导的神经元损伤具有保护作用,与抑制TNF-α、IL-1β及Cys LTs的释放有关。Objective To investigate the effect of 1,8-cineol against Aβ(25 ~ 35)-induced inflammatory response in rat primary cultured neurons. Methods Rat primary cultured cortical neurons were randomly divided into control,Aβ(25 ~ 35)( 20 μmol/L),low dose of 1,8-cineol( Aβ(25 ~ 35)20 μmol / L + 1,8-cineol 1 μmol / L),high dose of 1,8-cineol( Aβ(25 ~ 35)20 μmol / L +1,8-cineol 10 μmol / L) groups. Cell viability was evaluated by 3-( 4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide( MTT) reduction assay. Neuron injury was induced24 h after Aβ(25 ~ 35) treatment. Releases of TNF-α,IL-1β and Cys LTs in the supernatant were determined by ELISA. Results 20 μmol / L of Aβ(25 ~ 35) incubated for 24 h significantly reduced neuronal activity,and increased TNF-α,IL-1β and Cys LTs releases. Pretreatment with 1,8-cineol obviously inhibited cytotoxicity and decreased the level of above cytokines and Cys LTs releases. Conclusions 1,8-cineol has a protective effect on Aβ(25 ~ 35) induced neuron injury,probably relates with inhibition of TNF-α,IL-1β and Cys LTs releases.
分 类 号:R749.1[医药卫生—神经病学与精神病学]
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