STUDIES ON NEW, CENTRALLY ACTIVE AND REVERSIBLE ACETYLCHOLINESTERASE INHIBITORS

被引:13
作者
ARNAL, F
COTE, LJ
GINSBURG, S
LAWRENCE, GD
NAINI, A
SANO, M
机构
[1] COLUMBIA UNIV COLL PHYS & SURG,DEPT NEUROL,NEW YORK,NY 10032
[2] LONG ISL UNIV,DEPT CHEM,BROOKLYN,NY 11201
关键词
Acetylcholinesterase inhibitors; mouse brain; physostigmine; tetrahydroaminoacridine;
D O I
10.1007/BF00973747
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have synthesized the tertiary amines of pyridostigmine and neostigmine, 3-pyridinol dimethylcarbamate (norpyridostigmine) and 3-dimethylaminophenol dimethylcarbamate (norneostigmine) respectively, and we have tested their abilities to cross the blood-brain barrier and inhibit mouse brainAChE activity. The in vivo inhibition of AChE activity by norpyridostigmine reaches 72% at 10 minutes which is comparable to that seen with physostigmine (73% at 10 minutes). Inhibition by norneostigmine is less effective (50% at 10 minutes) and approaches that obtained with tetrahydroaminoacridine (57% at 10 minutes). These data show that both norpyridostigmine and norneostigmine cross the blood-brain barrier and that they are effective inhibitors of mouse brain AChE activity. These drugs could be useful in the treatment of memory, impairment associated with Alzheimer's disease, and other memory disorders. © 1990 Plenum Publishing Corporation.
引用
收藏
页码:587 / 591
页数:5
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