Differential expression of pre- and postsynaptic GABAB receptors in rat substantia nigra pars reticulata neurones

被引:29
作者
Chan, PKY [1 ]
Leung, CKS [1 ]
Yung, WH [1 ]
机构
[1] Chinese Univ Hong Kong, Fac Med, Dept Physiol, Hong Kong, Peoples R China
关键词
substantia nigra; baclofen; GABA(B) receptor;
D O I
10.1016/S0014-2999(98)00194-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Whole-cell recordings were made from substantia nigra pars reticulata in rat midbrain slices to study the functional expression of pre- and postsynaptic GABA(B) receptors in GABA output neurones. Baclofen (up to 300 mu M) dose-dependently activated a weak current which was insensitive to tetrodotoxin and Ca2+-free solution but blocked by Ba2+ and 2-OH-saclofen. The maximum current activated by baclofen (30 mu M) was 43.0 +/- 4.5 pA (n = 27), representing only 23% of that in dopamine neurones. Baclofen (1-30 mu M) also reduced the frequency of the GABA(A) receptor-mediated miniature inhibitory postsynaptic currents while the distribution of their amplitudes was unaffected. This presynaptic effect of baclofen, prominent at a concentration as low as 1 mu M, was sensitive to 2-OH-saclofen and occluded by Cd2+, but was unaffected by Ba2+. The results suggest a predominant role of the presynaptic GABA(B) receptors in substantia nigra pars reticulata. The relative abundance of pre- and postsynaptic GABA(B) receptor subtypes in this brain region may also be important in mediating the anticonvulsant effect of baclofen in rats. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:187 / 197
页数:11
相关论文
共 44 条
[1]   GABA-A AND GABA-B RECEPTOR-SITE DISTRIBUTION IN THE RAT CENTRAL-NERVOUS-SYSTEM [J].
BOWERY, NG ;
HUDSON, AL ;
PRICE, GW .
NEUROSCIENCE, 1987, 20 (02) :365-383
[2]   DISINHIBITION AS A BASIC PROCESS IN THE EXPRESSION OF STRIATAL FUNCTIONS [J].
CHEVALIER, G ;
DENIAU, JM .
TRENDS IN NEUROSCIENCES, 1990, 13 (07) :277-280
[3]   DISTRIBUTION AND KINETICS OF GABA-B BINDING-SITES IN RAT CENTRAL-NERVOUS-SYSTEM - A QUANTITATIVE AUTORADIOGRAPHIC STUDY [J].
CHU, DCM ;
ALBIN, RL ;
YOUNG, AB ;
PENNEY, JB .
NEUROSCIENCE, 1990, 34 (02) :341-357
[4]   ENDOGENOUS CONTROL OF EPILEPSY - THE NIGRAL INHIBITORY SYSTEM [J].
DEPAULIS, A ;
VERGNES, M ;
MARESCAUX, C .
PROGRESS IN NEUROBIOLOGY, 1994, 42 (01) :33-52
[5]   CALCIUM-CHANNEL INVOLVEMENT IN GABA(B) RECEPTOR-MEDIATED INHIBITION OF GABA RELEASE IN AREA CA1 OF THE RAT HIPPOCAMPUS [J].
DOZE, VA ;
COHEN, GA ;
MADISON, DV .
JOURNAL OF NEUROPHYSIOLOGY, 1995, 74 (01) :43-53
[6]   PRESYNAPTIC MODULATION OF THE RELEASE OF GABA BY GABAA RECEPTORS IN PARS COMPACTA AND BY GABAB RECEPTORS IN PARS RETICULATA OF THE RAT SUBSTANTIA NIGRA [J].
FLORAN, B ;
SILVA, I ;
NAVA, C ;
ACEVES, J .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 150 (03) :277-286
[7]   GABAB-RECEPTOR-ACTIVATED K+ CURRENT IN VOLTAGE-CLAMPED CA3 PYRAMIDAL CELLS IN HIPPOCAMPAL CULTURES [J].
GAHWILER, BH ;
BROWN, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (05) :1558-1562
[8]   REPUDIATION AND RENEGOTIATION - THE CASE OF SOVEREIGN DEBT [J].
GALE, D ;
HELLWIG, M .
INTERNATIONAL ECONOMIC REVIEW, 1989, 30 (01) :3-31
[9]   THE DENSITY OF GABA-B BINDING-SITES IN THE SUBSTANTIA-NIGRA IS GREATER IN RAT PUPS THAN IN ADULTS [J].
GARANT, D ;
SPERBER, E ;
MOSHE, S .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 214 (01) :75-78
[10]   GABA TERMINAL AUTORECEPTORS IN THE PARS COMPACTA AND IN THE PARS RETICULATA OF THE RAT SUBSTANTIA NIGRA ARE GABAB [J].
GIRALT, MT ;
BONANNO, G ;
RAITERI, M .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 175 (02) :137-144