Role of astrocytes in the maintenance and modulation of glutamatergic and GABAergic neurotransmission

被引:153
作者
Schousboe, A [1 ]
机构
[1] Royal Danish Sch Pharm, Dept Pharmacol, DK-2100 Copenhagen, Denmark
关键词
epilepsy; neurodegeneration; glia; neurons; GABA-transporters; glutamate-transporters;
D O I
10.1023/A:1022397704922
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The functional activity in the brain is primarily composed of an interplay between excitation and inhibition. In any given region the output is based upon a complex processing of incoming signals that require both excitatory and inhibitory units. Moreover, these units must be regulated and balanced such that an integrated and finely tuned response is generated. In each of these units or synapses the activity depends on biosynthesis, release, receptor interaction, and inactivation of the neurotransmitter in question; thus, it is easily understood that each of these processes needs to be highly regulated and controlled. It is interesting to note that in case of the most prevailing neurotransmitters, glutamate and GABA, which mediate excitation and inhibition, respectively, the inactivation process is primarily maintained by highly efficient, high-affinity transport systems capable of maintaining transmembrane concentration gradients of these amino acids of 10(4)-10(5)-fold. The demonstration of the presence of transporters for glutamate and GABA in both neuronal and astrocytic elements naturally raises the question of the functional importance of the astrocytes in the regulation of the level of the neurotransmitters in the synaptic cleft and hence for the activity of excitatory and inhibitory neurotransmission. Obviously, this discussion has important implications for the understanding of the role of astrocytes in disease states in which imbalances between excitation and inhibition are a triggering factor, for example, epilepsy and neurodegeneration.
引用
收藏
页码:347 / 352
页数:6
相关论文
共 87 条
[11]   THE HIGH-AFFINITY UPTAKE SYSTEM FOR EXCITATORY AMINO-ACIDS IN THE BRAIN [J].
DANBOLT, NC .
PROGRESS IN NEUROBIOLOGY, 1994, 44 (04) :377-396
[12]  
Davis KE, 1998, J NEUROSCI, V18, P2475
[13]   Immunoreactivity for the GABA transporter-1 and GABA transporter-3 is restricted to astrocytes in the rat thalamus. A light and electron-microscopic immunolocalization [J].
De Biasi, S ;
Vitellaro-Zuccarello, L ;
Brecha, NC .
NEUROSCIENCE, 1998, 83 (03) :815-828
[14]  
Dehnes Y, 1998, J NEUROSCI, V18, P3606
[15]   Rapid stimulation of EAAC1-mediated Na+-dependent L-glutamate transport activity in C6 glioma cells by phorbol ester [J].
Dowd, LA ;
Robinson, MB .
JOURNAL OF NEUROCHEMISTRY, 1996, 67 (02) :508-516
[16]   NOVEL NEURON-RELATED REGULATORY MECHANISMS FOR ASTROCYTIC GLUTAMATE AND GABA HIGH-AFFINITY UPTAKE [J].
DREJER, J ;
MEIER, E ;
SCHOUSBOE, A .
NEUROSCIENCE LETTERS, 1983, 37 (03) :301-306
[17]   SYSTEMIC CI-966, A NEW GAMMA-AMINOBUTYRIC-ACID UPTAKE BLOCKER, ENHANCES GAMMA-AMINOBUTYRIC-ACID ACTION IN CA1 PYRAMIDAL LAYER INSITU [J].
EBERT, U ;
KRNJEVIC, K .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1990, 68 (09) :1194-1199
[18]   AN EXCITATORY AMINO-ACID TRANSPORTER WITH PROPERTIES OF A LIGAND-GATED CHLORIDE CHANNEL [J].
FAIRMAN, WA ;
VANDENBERG, RJ ;
ARRIZA, JL ;
KAVANAUGH, MP ;
AMARA, SG .
NATURE, 1995, 375 (6532) :599-603
[19]   Selective inhibitors of glial GABA uptake:: Synthesis, absolute stereochemistry, and pharmacology of the enantiomers of 3-hydroxy-4-amino-4,5,6,7-tetrahydro-1,2-benzisoxazole (exo-THPO) and analogues [J].
Falch, E ;
Perregaard, J ;
Frolund, B ;
Sokilde, B ;
Buur, A ;
Hansen, LM ;
Frydenvang, K ;
Brehm, L ;
Bolvig, T ;
Larsson, OM ;
Sanchez, C ;
White, HS ;
Schousboe, A ;
Krogsgaard-Larsen, P .
JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (26) :5402-5414
[20]   THE GAMMA-AMINOBUTYRIC-ACID (GABA) UPTAKE INHIBITOR, TIAGABINE, INCREASES EXTRACELLULAR BRAIN LEVELS OF GABA IN AWAKE RATS [J].
FINKJENSEN, A ;
SUZDAK, PD ;
SWEDBERG, MDB ;
JUDGE, ME ;
HANSEN, L ;
NIELSEN, PG .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 220 (2-3) :197-201