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作 者:薛小燕[1,3] 章正[2,4] 周晓雯[2,3] 周星[2,3] 罗焕敏[2,3]
机构地区:[1]赣州市人民医院,江西赣州341000 [2]暨南大学-香港大学脑功能与健康联合实验室,广东广州510632 [3]暨南大学医学院药理学系,广东广州510632 [4]暨南大学附属第一医院,广东广州510632
出 处:《中药材》2012年第11期1813-1816,共4页Journal of Chinese Medicinal Materials
基 金:国家自然科学基金(30672456);广东省科技计划项目(2010B030700018)
摘 要:目的:探讨原儿茶酸对M146L细胞APP mRNA表达的影响,寻找潜在的具有抑制Aβ分泌的中药单体,以达到治疗阿尔茨海默病(Alzheimer's disease,AD)的目的。方法:体外培养稳定转染人类阿尔茨海默病β淀粉样蛋白前体(amyloidβ-protein precursor,APP)基因及突变型早老素1(prsenilin-1,PS1)基因的CHO(Chinese hamsterovary cells)细胞系(M146L),使之高效产生β淀粉样蛋白42(amyloidβ-protein,Aβ42),建立Aβ42过度表达的细胞模型。加入待筛选的药物原儿茶酸,用MTT比色法检测不同浓度的原儿茶酸(0.25、0.5、1.0、2.0 mmol/L)对M146L细胞的毒性作用,应用RT-PCR法检测原儿茶酸对M146L细胞APP mRNA表达的影响。结果:浓度0.25、0.5、1.0mmol/L的原儿茶酸对M146L细胞存活率无明显影响,不具有细胞毒性作用,对M146L细胞APP mRNA表达有抑制作用,并呈剂量依赖性。结论:一定剂量的原儿茶酸对M146L细胞APP mRNA表达有明显的抑制作用,其机制有待进一步研究。Objective: To investigate the effect of protocatechuie acid on the mRNA expression of APP in double transfected ( hu- man APP gene and presenlin-1 gene) Chinese hamster ovary (CHO) cells (M146L). Methods:A/342 overexpressing cell model was es- tablished in vitro by culturing Chinese hamster ovary cells stably expressing amyloid beta-protein precursor and mutant presenilin (M146L). The MTr assay was used to test cytotoxicity of protocatechuic acid, and reverse transcription polymerase chain reaction ( RT- PCR) was carried out to determine the mRNA expression level of APP. Results :The MTY assay showed that protocatechuie acid at suit- able concentrations didn't have cytotoxicity on M146L cell survival. Protocatechuic acid at the concentration of 0. 25 mmol/L,0. 5 mmol/L and 1.0 mmol/L significantly inhibited the mRNA expression of APP. Conclusion:The study suggests that the suitable dose of protocatechuic acid could inhibit the mRNA expression of APP in M146L cell, and its mechanism needs further study.
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