CHOLINESTERASE-INHIBITORS INCREASE SECRETION OF APPS IN RAT-BRAIN CORTEX

被引:158
作者
MORI, F [1 ]
LAI, CC [1 ]
FUSI, F [1 ]
GIACOBINI, E [1 ]
机构
[1] SO ILLINOIS UNIV,SCH MED,DEPT PHARMACOL,SPRINGFIELD,IL 62794
关键词
APPS; BETHANECHOL; PHYSOSTIGMINE; HEPTYL-PHYSOSTIGMINE; DDVP;
D O I
10.1097/00001756-199503000-00012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
WE examined whether cholinesterase inhibitors (ChEI) could alter the release of amyloid precursor protein (APP) from superfused brain cortical slices of the rat. Three ChEI, both reversible and irreversible, were tested for their ability to enhance the release of nonamyloidogenic soluble derivatives (APPs). These included: physostigmine (PHY), heptyl-physostigmine (HEP) and 2,2-dichlorovinyldimethyl phosphate (DDVP), at concentrations producing cholinesterase (ChE) inhibition ranging from 5% to 95%. All three ChEI elevated APPs release significantly above control levels. Electrical field stimulation significantly increased the release of APPs within 50 min. Similar increase was observed after muscarinic receptor stimulation with bethanechol (BETHA). Tetrodotoxin (TTX) completely blocked the effect of electrical stimulation. These findings suggest that administration of ChEI to Alzheimer's disease (AD) patients may have a neuroprotective effect by activating normal APP processing.
引用
收藏
页码:633 / 636
页数:4
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