Rapid activation of microglial cells by hypoxia, kainic acid, and potassium ions in slice preparations of the rat hippocampus

被引:28
作者
Abrahám, H
Losonczy, A
Czéh, G
Lázár, G
机构
[1] Univ Pecs, Fac Med, Dept Human Anat, H-7643 Pecs, Hungary
[2] Univ Pecs, Fac Med, Dept Pharmacol & Pharmacotherapy, H-7643 Pecs, Hungary
[3] Univ Pecs, Fac Med, Cent Electron Microscop Lab, H-7643 Pecs, Hungary
关键词
electrophysiology; glial reaction; immunohistochemistry; OX-42; antibody;
D O I
10.1016/S0006-8993(01)02569-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Microglial activation induced by hypoxia, kainic acid and elevated potassium concentration, all of which alter neuronal function, was studied in hippocampal slices. The activation of microglia was detected by immunostaining with a monoclonal antibody (OX-42) raised against a type 3 complement receptor (CD11b). During activation the phenotype of microglia changes and the intensity of staining of individual cells increases. Oxygen deprivation depressed the focal responses of CA1 neurons to stratum radiatum volleys. Microglial activation was time dependent. Ten minute hypoxia caused mild activation, and after 20 min, a strong microglial reaction could be observed. Although neuronal function returned during reoxygenation, the morphological signs of microglial activation remained. Epileptiform activity of hippocampal neurons, followed by depression. was induced by application of 0.5 mM kainic acid, in a time and dose dependent manner. Washing out kainic acid did not alter microglial reaction. Elevated concentrations of potassium ions induced microglial changes similar to those induced by hypoxia and kainic acid. It is therefore suggested that an elevated extracellular potassium ion concentration may be the common factor in microglial activation observed in these experiments since this is raised both in hypoxia and under the effect of excitotoxins, (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:115 / 126
页数:12
相关论文
共 37 条
[1]   Early microglial reaction following mild forebrain ischemia induced by common carotid artery occlusion in rats [J].
Abrahám, H ;
Lázár, G .
BRAIN RESEARCH, 2000, 862 (1-2) :63-73
[2]   EARLY RESPONSE OF BRAIN RESIDENT MICROGLIA TO KAINIC ACID-INDUCED HIPPOCAMPAL-LESIONS [J].
AKIYAMA, H ;
TOOYAMA, I ;
KONDO, H ;
IKEDA, K ;
KIMURA, H ;
MCGEER, EG ;
MCGEER, PL .
BRAIN RESEARCH, 1994, 635 (1-2) :257-268
[3]   Interleukin-1β activates forebrain glial cells and increases nitric oxide production and cortical glutamate and GABA release in vivo:: Implications for Alzheimer's disease [J].
Casamenti, F ;
Prosperi, C ;
Scali, C ;
Giovannelli, L ;
Colivicchi, MA ;
Faussone-Pellegrini, MS ;
Pepeu, G .
NEUROSCIENCE, 1999, 91 (03) :831-842
[4]  
CREPEL V, 1989, NEUROSCIENCE, V3, P605
[5]  
Czéh B, 1998, HIPPOCAMPUS, V8, P548
[6]  
Dingledine R, 1999, PHARMACOL REV, V51, P7
[7]  
Elkabes S, 1996, J NEUROSCI, V16, P2508
[8]   MICROGLIAL MHC ANTIGEN EXPRESSION AFTER ISCHEMIC AND KAINIC ACID LESIONS OF THE ADULT-RAT HIPPOCAMPUS [J].
FINSEN, BR ;
JORGENSEN, MB ;
DIEMER, NH ;
ZIMMER, J .
GLIA, 1993, 7 (01) :41-49
[9]  
GERHMANN J, 1992, J CEREB BLOOD FLOW M, V12, P257
[10]   Expression of ionotropic glutamate receptor subunits in glial cells of the hippocampal CA1 area following transient forebrain ischemia [J].
Gottlieb, M ;
Matute, C .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1997, 17 (03) :290-300