中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Anticholinesterase effects of huperzine A, E2020, and tacrine in rats

文献类型:期刊论文

作者Wang, H; Tang, XC
刊名ACTA PHARMACOLOGICA SINICA
出版日期1998-01
卷号19期号:1页码:27-30
关键词cholinesterase inhibitors cholinesterases huperzine A E2020 tacrine
ISSN号0253-9756
文献子类Article
英文摘要AIM: To compare the anticholinesterase effects of huperzine A (Hup A), E2020, and tacrine in rats. METHODS: Spectrophotometry was used to determine AChE activity in brain and BuChE activity in serum. RESULTS: Following intragastric gavage, Hup A, E2020, and tacrine all produced dose-dependent inhibitions of brain AChE. Oral Hup A exhibited a higher inhibition than E2020 and tacrine. Tacrine was more effective in inhibiting serum BuChE correlated with severe peripheral adverse effects. The BuChE activity was less affected by Hup A and E2020. After a single oral dose of Hup A, a relatively steady state of AChE inhibition produced, which was longer than that after E2020 and tacrine. No change in the cholinesterase inhibition was seen for the 3 drugs following repeated ig medications. CONCLUSION: Hup A ig exhibited a higher efficacy, a longer duration of action, and a more selective inhibition on AChE than E2020 and tacrine.
WOS关键词ALZHEIMERS-DISEASE ; PHYSOSTIGMINE
WOS研究方向Chemistry ; Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000071424500007
出版者ACTA PHARMACOLOGICA SINICA
源URL[http://119.78.100.183/handle/2S10ELR8/274866]  
专题院士及顾问专家
中科院受体结构与功能重点实验室
新药研究国家重点实验室
药物安全性评价中心
通讯作者Tang, XC
作者单位Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 200031, Peoples R China
推荐引用方式
GB/T 7714
Wang, H,Tang, XC. Anticholinesterase effects of huperzine A, E2020, and tacrine in rats[J]. ACTA PHARMACOLOGICA SINICA,1998,19(1):27-30.
APA Wang, H,&Tang, XC.(1998).Anticholinesterase effects of huperzine A, E2020, and tacrine in rats.ACTA PHARMACOLOGICA SINICA,19(1),27-30.
MLA Wang, H,et al."Anticholinesterase effects of huperzine A, E2020, and tacrine in rats".ACTA PHARMACOLOGICA SINICA 19.1(1998):27-30.

入库方式: OAI收割

来源:上海药物研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。