PROPENTOSYLLINE DEPRESSES AMYLOID AND ALZHEIMERS CSF MICROGLIAL ANTIGENS AFTER ISCHEMIA

被引:37
作者
MCRAE, A
RUDOLPHI, KA
SCHUBERT, P
机构
[1] MAX PLANCK INST PSYCHIAT,DEPT NEUROMORPHOL,D-82152 MARTINSRIED,GERMANY
[2] GOTHENBURG UNIV,GOTHENBURG,SWEDEN
[3] HOECHST AG,W-6230 FRANKFURT,GERMANY
关键词
PROPENTOSYLLINE; ADENOSINE; AMYLOID PRECURSOR PROTEIN; ALZHEIMERS DISEASE; ANTIGEN EXPRESSION; MICROGLIA ACTIVATION; ISCHEMIA; GERBIL HIPPOCAMPUS;
D O I
10.1097/00001756-199406020-00008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
IN the gerbil hippocampus activated microglial antigens are intensely stained by cerebrospinal fluid from patients with Alzheimer's disease (AD-CSF), OXl8 and the amyloid precursor protein (beta-APP) up to 14 days after ischaemia. Propentosylline (PPF), which facilitates the adenosine A2 receptor action, has been shown to be neuroprotective, to depress O-2(-) radical formation in macrophages and to interfere with the generation of phagocytotic macrophages from cultivated microglial cells. In this report we tested in ischaemic gerbils whether PPF treatment influences the potential neurotoxic properties of microglia. Daily post-treatment with PPF, started 24 h after ischaemia, depressed the immunostaining of activated microglia by AD-CSF, OX18 and APP in the hippocampus. Thus, PPF may protect against microglia-related brain damage.
引用
收藏
页码:1193 / 1196
页数:4
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