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作 者:刘四军[1] 陈惠芳[2] 张一帆[2] 王莹莹[2] 陈云波[2] 王奇[2]
机构地区:[1]广州中医药大学中药学院,广东广州510006 [2]广州中医药大学临床药理研究所,广东广州510006
出 处:《中药新药与临床药理》2016年第1期54-57,共4页Traditional Chinese Drug Research and Clinical Pharmacology
基 金:广州中医药大学优秀青年学者科研基金(201303);广东省自然科学基金项目(2015A030310414);教育部高等学校博士学科点专项科研基金(20114425110007)
摘 要:目的探索β-细辛醚对于阿尔茨海默病(Alzheimer's Disease,AD)细胞模型的作用及其可能机制。方法选用Aβ1-42的浓度为10μmol·L^(-1)作为建模条件,以NG108-15细胞为研究对象,建立体外AD细胞模型,β-细辛醚低、中、高剂量组(6.25,12.5,25μmol·L^(-1))分别进行干预,通过MTT法检测细胞活力,并观察β-细辛醚对细胞形态学的影响以及Wesstern blot法检测细胞突触的相关功能蛋白突触素蛋白(Synaptophysin,SYP)、以及AMPA受体亚单位(Glutamatergic receptor 2,GluR2)的表达。结果 MTT结果显示,β-细辛醚高剂量组干预24 h后能显著减轻Aβ1-42的毒性损伤(P<0.05)。从细胞形态上看,细辛醚各剂量组跟模型组差异显著,跟溶媒对照组比较无明显差异。与模型组SYP相对表达量比较,溶媒对照组、β-细辛醚中、高剂量组差异均有统计学意义(P<0.05)。β-细辛醚中、高剂量组的SYP表达量显著上调。而各组GluR2相对表达量比较,差异均无统计学意义(P>0.05)。结论β-细辛醚高剂量组能显著改善细胞形态以及提高细胞活力,具有一定的神经保护作用,可能是通过上调SYP的表达,从而影响突触功能,改善认知。Objective To explore the effect and the possible mechanism of β-asarone on Alzheimer's disease(AD)in-vitro cell model. Methods Selecting 10 μmol·L^(-1)A β1-42 as modeling conditions and using NG108-15 cells as the research object,we established the AD cell model in vitro. After the cell model was treated with different doses ofβ-asarone(6.25,12.5,25 μmol·L^(-1)),we detected the cell viability by MTT method,and investigated the effects ofβ-asarone on cell morphology and on the expression of synaptophysin(SYP)and glutamatergic receptor 2(Glu R2).Results The MTT assay results showed that 25 μmol·L^(-1) of treatment with high dose of β-asarone for 24 h significantly reduced the toxicity of Aβ1-42(P〈0.05). The results of morphological examination showed that the difference of cell morphology was significant between the three β-asarone groups and model group, but was insignificant betweenβ-asarone groups and the normal group. Compared with the model group,SYP relative expression in medium- and high-dose β-asarone groups was up-regulated(P〈0.05). However,the difference of Glu R2 relative expression was not significant between any two groups(P〈0.05). Conclusion β-asarone at 25 μmol/L could significantly improve the cell morphology and improve the cell vitality,and its neuroprotective mechanism is possibly related to upregulating the expression of SYP,thereby affecting synaptic function and improving cognition.
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