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作 者:罗景慧[1] 杨迎暴[2] 林永成[1] 陈志良[3] 吴雄宇[1]
机构地区:[1]中山大学化学与化工学院,广州510275 [2]第一军医大学,广州510515 [3]南方医院药学部,广州510515
出 处:《中药材》2004年第4期261-264,共4页Journal of Chinese Medicinal Materials
基 金:国家 8 63 ( 2 0 0 1AA62 40 10 );国家自然科学基金( 2 0 0 72 0 5 8;2 9672 0 5 3 );广东省自然科学基金( 95 0 0 2 6;0 80 3 17);广东省自然科学基金重点项目( 0 2 173 2 )资助项目
摘 要:目的 :体外研究中国南海海岸红树林真菌Xylariasp 代谢产物XyloketalA~D对乙酰胆碱酯酶(AChE)活性的影响。方法 :采用改良Ellmen法测定AChE活性 ,考察受试化合物在体外对AChE活性及其酶动力学特征的影响 ,并就这些化合物对AChE和丁酰胆碱酯酶 (BuChE)的选择性进行比较。结果 :xyloketalA~D在体外对AChE活性均有不同程度的抑制作用 ,并呈一定剂量依赖关系 ,IC50 值分别为 2 9 9、137 4、10 9 3和 4 2 5 6μmol/L。通过对AChE酶抑制动力学曲线进行分析发现 ,xyloketals对AChE的抑制表现为可逆非竞争性抑制。此外 ,对于另一种胆碱酯酶BuChE ,阳性药维那克林及xyloketals均表现出一定降低作用 ,但相对而言xyloketals对AChE的选择性较强。结论 :xlylketals在体外对AChE活性有可逆非竞争性抑制作用 ,表明该类化合物可能作为抗早老性痴呆 (AD)药物进行开发 ,同时该结果亦提示 。Objective:To investigate the effects of metabolites of mangrove fungus Xylaria sp from South China Sea Coast,xyloketal A~D,on the activity of acetylcholinesterase (AChE) in vitro Methods:Activity of AChE was determined by a modified method of Ellmen The selectivity of the compounds for AChE and butyrylcholinesterase (BuChE) was also tested and compared with that of a positive control,velnacrine. The inhibitory properties of xylokets on AChE were characterized as well Results:AChE activity was inhibited by xyloketal A~D in a dose dependent manner, their IC 50 were determined to be 29 9,137 4,109 3 and 425 6 μmol/L,respectively At the same time,velnacrine and all the four compounds showed inhibitory effects on BuChE in different degree,and the inhibitory activity of xyloketals on AChE was found to be reversible and noncompetitive Conclusion: Xyloketal A~D can inhibit AChE as well as BuChE activity in vitro. So xyloketal A~D were likely considered as drug candidates against Alzheimer's disease (AD) for further development.
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