中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Novel Anti-Alzheimer's Dimer Bis(7)-Cognitin: Cellular and Molecular Mechanisms of Neuroprotection Through Multiple Targets

文献类型:期刊论文

作者Li, Wenming4; Mak, Marvin4; Jiang, Hualiang3; Wang, Qinwen1; Pang, Yuanping2; Chen, Kaixian3; Han, Yifan4
刊名NEUROTHERAPEUTICS
出版日期2009-01
卷号6期号:1页码:187-201
关键词Bis(7)-Cognitin multiple targets neuroprotection AChE NMDA receptor
ISSN号1933-7213
DOI10.1016/j.nurt.2008.10.040
文献子类Review
英文摘要Alzheimer's disease (AD) is a progressive and degenerative brain disorder that has emerged as one of the major public health problems in adults. Unfortunately, its molecular pathology and therapeutic strategies remain elusive. Because there are multiple factors closely indicated in the pathogenesis of AD, multiple drug therapy will be required to address the varied pathological aspects of this disease. Existing pharmacological approaches with one-molecule-one-target are limited in their ability to modify the pathology of AD. Novel therapeutics strategies comprise multifunctional compounds specifically designed to target concurrently on different sites at multifactorial etiopathogenesis of AD, thereby providing greater therapeutic efficacy. Over the past decade, our group has developed several series of dimeric acetylcholinesterase (AChE) inhibitors derived from tacrine and huperzine A, a unique anti-Alzheimer's drug originally discovered from a traditional Chinese medicinal plant. Bis(7)-Cognitin, one of our novel dimers, through inhibition of AChE, N-methyl-D-aspartate receptor, nitric oxide synthase, and amyloid precursor protein/beta-amyloid cascade concurrently, possesses remarkable neuroprotective activities. More importantly, the synergism between these targets might serve as one of the most effective therapeutic strategies to arrest/modify pathological process of AD in addition to improving the cognitive functions for AD.
WOS关键词AMYLOID-BETA-PEPTIDE ; INDUCED NEURONAL APOPTOSIS ; D-ASPARTATE RECEPTORS ; HUPERZINE-A ; ACETYLCHOLINESTERASE INHIBITOR ; TORPEDO-CALIFORNICA ; NAVIGATIONAL MEMORY ; PRECURSOR PROTEIN ; COMBAT ALZHEIMERS ; DISEASE
资助项目Research Grants Council of Hong Kong[PolyU6441/06M] ; Research Grants Council of Hong Kong[6608/07M] ; Research Grants Council of Hong Kong[N_PolyU618/07] ; Hong Kong PolyU[G-YX96] ; Hong Kong PolyU[G-U439] ; Ministry of Science and Technology (MOST) of China[2008CB517411] ; Shenzhen Shuangbai Scheme[00000000]
WOS研究方向Neurosciences & Neurology ; Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000261983100016
出版者SPRINGER
源URL[http://119.78.100.183/handle/2S10ELR8/279400]  
专题药物发现与设计中心
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
通讯作者Han, Yifan
作者单位1.Ningbo Univ, Sch Med, Dept Physiol, Ningbo 315211, Zhejiang, Peoples R China
2.Mayo Fdn Med Educ & Res, Rochester, MN 55905 USA;
3.Shanghai Inst Mat Media, State Key Lab Drug Res, Ctr Drug Discovery & Design, Shanghai 201203, Peoples R China;
4.Hong Kong Polytech Univ, Inst Modern Chinese Med, Dept Appl Biol & Chem Technol, Hong Kong, Hong Kong, Peoples R China;
推荐引用方式
GB/T 7714
Li, Wenming,Mak, Marvin,Jiang, Hualiang,et al. Novel Anti-Alzheimer's Dimer Bis(7)-Cognitin: Cellular and Molecular Mechanisms of Neuroprotection Through Multiple Targets[J]. NEUROTHERAPEUTICS,2009,6(1):187-201.
APA Li, Wenming.,Mak, Marvin.,Jiang, Hualiang.,Wang, Qinwen.,Pang, Yuanping.,...&Han, Yifan.(2009).Novel Anti-Alzheimer's Dimer Bis(7)-Cognitin: Cellular and Molecular Mechanisms of Neuroprotection Through Multiple Targets.NEUROTHERAPEUTICS,6(1),187-201.
MLA Li, Wenming,et al."Novel Anti-Alzheimer's Dimer Bis(7)-Cognitin: Cellular and Molecular Mechanisms of Neuroprotection Through Multiple Targets".NEUROTHERAPEUTICS 6.1(2009):187-201.

入库方式: OAI收割

来源:上海药物研究所

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