Role of astrocytes in grey matter during stroke: A modelling approach

被引:18
作者
Dronne, Marie-Aimee
Grenier, Emmanuel
Dumont, Thierry
Hommel, Marc
Boissel, Jean-Pierre
机构
[1] Univ Lyon 1, CNRS, UMR 5558, Inst Med Theor, F-69365 Lyon, France
[2] Ecole Normale Super, Unite Math Pures & Appliquees, Lyon, France
[3] Univ Lyon 1, CNRS, UMR 5208, Inst Camille Jordan, Villeurbanne, France
[4] Univ Grenoble 1, INSERM, CHU, UMR U594,Serv Neurol, Grenoble, France
关键词
mathematical model; simulations; ischaemia; excitotoxicity; potassium; glutamate;
D O I
10.1016/j.brainres.2006.12.062
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The astrocytic response to stroke is extremely complex and incompletely understood. On the one hand, astrocytes are known to be neuroprotective when extracellular glutamate or potassium is slightly increased. But, on the other hand, they are considered to contribute to the extracellular glutamate increase during severe ischaemia. A mathematical model is used to reproduce the dynamics of the membrane potentials, intracellular and extracellular concentrations and volumes of neurons and astrocytes during ischaemia in order to study the role of astrocytes in grey matter during the first hour of a stroke. Under conditions of mild ischaemia, astrocytes are observed to take up glutamate via the glutamate transporter, and potassium via the Na/K/Cl cotransporter, which limits glutamate and potassium increase in the extracellular space. On the contrary, under conditions of severe ischaemia, astrocytes appear to be unable to maintain potassium homeostasis. Moreover, they are shown to contribute to the excitotoxicity process by expelling glutamate out of the cells via the reversed glutamate transporter. A detailed understanding of astrocytic function and influence on neuron survival during stroke is necessary to improve the neuroprotective strategies for stroke patients. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:231 / 242
页数:12
相关论文
共 75 条
[61]  
STORMMATHISEN J, 1992, PROG BRAIN RES, V94, P225
[62]   ASTROCYTE GLUTAMATE UPTAKE DURING CHEMICAL HYPOXIA INVITRO [J].
SWANSON, RA .
NEUROSCIENCE LETTERS, 1992, 147 (02) :143-146
[63]  
Swanson RA, 1997, GLIA, V21, P142, DOI 10.1002/(SICI)1098-1136(199709)21:1<142::AID-GLIA16>3.0.CO
[64]  
2-S
[65]   NON-VESICULAR RELEASE OF GLUTAMATE FROM GLIAL-CELLS BY REVERSED ELECTROGENIC GLUTAMATE UPTAKE [J].
SZATKOWSKI, M ;
BARBOUR, B ;
ATTWELL, D .
NATURE, 1990, 348 (6300) :443-446
[66]  
Takahashi M, 1997, J EXP BIOL, V200, P401
[67]   Ion channels in glial cells [J].
Verkhratsky, A ;
Steinhäuser, C .
BRAIN RESEARCH REVIEWS, 2000, 32 (2-3) :380-412
[68]   OUABAIN-SENSITIVE AND OUABAIN-RESISTANT NET UPTAKE OF POTASSIUM INTO ASTROCYTES AND NEURONS IN PRIMARY CULTURES [J].
WALZ, W ;
HERTZ, L .
JOURNAL OF NEUROCHEMISTRY, 1982, 39 (01) :70-77
[69]   A TRANSMEMBRANE SODIUM CYCLE IN ASTROCYTES [J].
WALZ, W ;
HINKS, EC .
BRAIN RESEARCH, 1986, 368 (02) :226-232
[70]   FUNCTIONAL INTERACTIONS BETWEEN NEURONS AND ASTROCYTES .2. POTASSIUM HOMEOSTASIS AT THE CELLULAR-LEVEL [J].
WALZ, W ;
HERTZ, L .
PROGRESS IN NEUROBIOLOGY, 1983, 20 (1-2) :133-183