中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Inhibitory effects of huperzine B on cholinesterase activity in mice

文献类型:期刊论文

作者Liu, J; Zhang, HY; Wang, LM; Tang, XC
刊名ACTA PHARMACOLOGICA SINICA
出版日期1999-02
卷号20期号:2页码:141-145
关键词huperzine B tacrine cholinesterase inhibitors cholinesterases acetylcholinesterase brain cerebral cortex
ISSN号0253-9756
文献子类Article
英文摘要AIM: To determine the anticholinesterase properties of huperzine B (Hup B) and compare with tacrine in vitro and in vivo. METHODS: Spectrophotometry was used to determine ChE activity. RESULTS: Hup B showed much more selective inhibition to acetylcholinesterase (AChE) than tacrine. The IC50 ratios of Hup B and tacrine for butyrylcholinesterase (BuChE): AChE were 65.8 and 0.54, respectively. Hup B ig exhibited higher efficacy on the inhibition of brain AChE than that of tacrine. Tacrine was more effective in the inhibition of serum BuChE in mice with severe concomitant peripheral adverse effects than Hup B. A single ig dose of Hup B produced steady state of AChE inhibition in 4 h. CONCLUSION: Hup B exhibits higher selectivity and efficacy in the inhibition of AChE, and lower toxicity in mice than tacrine.
WOS关键词ALZHEIMERS-DISEASE ; TACRINE
WOS研究方向Chemistry ; Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000078533100010
出版者ACTA PHARMACOLOGICA SINICA
源URL[http://119.78.100.183/handle/2S10ELR8/274755]  
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
药物发现与设计中心
分析化学研究室
上海药物代谢研究中心
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
Liu, J,Zhang, HY,Wang, LM,et al. Inhibitory effects of huperzine B on cholinesterase activity in mice[J]. ACTA PHARMACOLOGICA SINICA,1999,20(2):141-145.
APA Liu, J,Zhang, HY,Wang, LM,&Tang, XC.(1999).Inhibitory effects of huperzine B on cholinesterase activity in mice.ACTA PHARMACOLOGICA SINICA,20(2),141-145.
MLA Liu, J,et al."Inhibitory effects of huperzine B on cholinesterase activity in mice".ACTA PHARMACOLOGICA SINICA 20.2(1999):141-145.

入库方式: OAI收割

来源:上海药物研究所

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