Protection against ischemic injury in primary cultured astrocytes of mouse cerebral cortex by bis(7)-tacrine, a novel anti-Alzheimer's agent

被引:41
作者
Han, YF
Wu, DC
Xiao, XA
Chen, PMY
Chung, W
Lee, NTK
Pang, YP
Carlier, PR
机构
[1] Hong Kong Univ Sci & Technol, Dept Biochem, Kowloon, Hong Kong, Peoples R China
[2] Mayo Clin & Mayo Fdn, Mayo Canc Ctr, Dept Pharmacol, Rochester, MN 55905 USA
[3] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Hong Kong, Peoples R China
关键词
bis(7)-tacrine; astrocyte; ischemia; acetylcholinesterase inhibitor;
D O I
10.1016/S0304-3940(00)01198-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of bis(7)-tacrine, a novel acetylcholinesterase inhibitor, on ischemia-induced cell death and apoptosis were investigated in primary cerebral cortical astrocytes of mice. Following a 6 h in vitro ischemic incubation of the cultures, a marked decrease in the percentage of viable cells was observed by lactate dehydrogenase (LDH) release assay. Furthermore, using bisbenzimide staining, we determined that approximately 65% of the cells underwent apoptosis. Treatment with bis(7)-tacrine (1-10 nM) during ischemic incubation effectively inhibited the ischemia-induced apoptosis, as demonstrated by morphological and biochemical tests. Our results demonstrated that bis(7)-tacrine could protect astrocytes against ischemia-induced cell injury, indicating that the drug might be beneficial for the treatment of vascular dementia, in addition to Alzheimer's disease. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:95 / 98
页数:4
相关论文
共 13 条
[1]   Is there a rationale for the use of acetylcholinesterase inhibitors in the therapy of Alzheimer's disease? [J].
Benzi, G ;
Moretti, A .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1998, 346 (01) :1-13
[2]  
Chen J, 1997, J NEUROCHEM, V69, P232
[3]   Bis(7)-tacrine, a novel acetylcholinesterase inhibitor, reverses AF64A-induced deficits in navigational memory in rats [J].
Liu, J ;
Ho, WL ;
Lee, NTK ;
Carlier, PR ;
Pang, YP ;
Han, YF .
NEUROSCIENCE LETTERS, 2000, 282 (03) :165-168
[4]   Highly potent, selective, and low cost bis-tetrahydroaminacrine inhibitors of acetylcholinesterase - Steps toward novel drugs for treating Alzheimer's disease [J].
Pang, YP ;
Quiram, P ;
Jelacic, T ;
Hong, F ;
Brimijoin, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (39) :23646-23649
[5]  
Peskind ER, 1998, J CLIN PSYCHIAT, V59, P22
[6]   ACCUMULATION OF EXTRACELLULAR GLUTAMATE AND NEURONAL DEATH IN ASTROCYTE-POOR CORTICAL CULTURES EXPOSED TO GLUTAMINE [J].
ROSENBERG, PA .
GLIA, 1991, 4 (01) :91-100
[7]   Cholinesterase inhibition improves blood flow in the ischemic cerebral cortex [J].
Scremin, OU ;
Li, MG ;
Scremin, AME ;
Jenden, DJ .
BRAIN RESEARCH BULLETIN, 1997, 42 (01) :59-70
[8]   GLUTAMATE, CALCIUM, AND FREE-RADICALS AS MEDIATORS OF ISCHEMIC BRAIN-DAMAGE [J].
SIESJO, BK ;
ZHAO, Q ;
PAHLMARK, K ;
SIESJO, P ;
KATSURA, K ;
FOLBERGROVA, J .
ANNALS OF THORACIC SURGERY, 1995, 59 (05) :1316-1320
[9]   ACETYLCHOLINESTERASE INHIBITOR ENA-713 PROTECTS AGAINST ISCHEMIA-INDUCED DECREASE IN PRESYNAPTIC AND POSTSYNAPTIC CHOLINERGIC INDEXES IN THE GERBIL BRAIN FOLLOWING TRANSIENT ISCHEMIA [J].
TANAKA, K ;
OGAWA, N ;
MIZUKAWA, K ;
ASANUMA, M ;
KONDO, Y ;
NISHIBAYASHI, S ;
MORI, A .
NEUROCHEMICAL RESEARCH, 1994, 19 (02) :117-122
[10]  
Wang H, 1999, ACTA PHARMACOL SIN, V20, P211