ANALYSIS OF THE HIPPOCAMPAL GABA(A) RECEPTOR SYSTEM IN KINDLED RATS BY AUTORADIOGRAPHIC AND IN-SITU HYBRIDIZATION TECHNIQUES - CONTINGENT TOLERANCE TO CARBAMAZEPINE

被引:49
作者
CLARK, M
MASSENBURG, GS
WEISS, SRB
POST, RM
机构
[1] Biological Psychiatry Branch, National Institute of Mental Health, Bethesda, MD 20892
来源
MOLECULAR BRAIN RESEARCH | 1994年 / 26卷 / 1-2期
关键词
GABA(A)-BENZODIAZEPINE RECEPTOR COMPLEX; MESSENGER-RNA; KINDLED SEIZURE; HIPPOCAMPUS; CARBAMAZEPINE; RECEPTOR AUTORADIOGRAPHY; CONTINGENT TOLERANCE; IN SITU HYBRIDIZATION;
D O I
10.1016/0169-328X(94)90104-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tolerance to the anticonvulsant effects of carbamazepine (CBZ) in the amygdala kindling paradigm is a contingent process, since it only develops in rats treated with CBZ before the kindling stimulation and not in those animals treated after the stimulation. The present study was designed to investigate the GABA(A) receptor system in CBZ contingent tolerance. Receptor autoradiography utilizing various radioligands that bind to different components of the GABA(A) receptor system and in situ hybridization with oligonucleotides that recognize different subunits of the GABA(A) receptor were performed. Kindling increased binding to benzodiazepine, picrotoxin, and GABA recognition sites selectively in the dentate gyrus of the hippocampus. Kindling also increased levels of mRNA for the alpha(4), beta(1), and beta(3) subunits but did not change alpha(1), alpha(2), or gamma(2), subunit levels. Rats tolerant to CBZ showed decreased [H-3]muscimol binding, diazepam-insensitive [H-3]Ro 15-4513 binding, and decreased alpha(4) subunit mRNA content compared to non-tolerant rats, whereas [H-3]flunitrazepam binding, [S-35]TBPS binding, and the levels of beta(1), and beta(3) Subunit mRNAs remained elevated. The data suggest an indirect interaction of CBZ with the GABA(A) receptor system, since CBZ reportedly does not bind to this receptor system.
引用
收藏
页码:309 / 319
页数:11
相关论文
共 41 条
[1]   CARBAMAZEPINE - A PHARMACOLOGICAL STUDY IN THE KINDLING MODEL OF EPILEPSY [J].
ALBERTSON, TE ;
JOY, RM ;
STARK, LG .
NEUROPHARMACOLOGY, 1984, 23 (10) :1117-1123
[2]   DEVELOPMENT OF A NEW PHARMACOLOGICAL SEIZURE MODEL - EFFECTS OF ANTICONVULSANTS ON CORTICAL-KINDLED AND AMYGDALA-KINDLED SEIZURES IN THE RAT [J].
ALBRIGHT, PS ;
BURNHAM, WM .
EPILEPSIA, 1980, 21 (06) :681-689
[3]  
BARNARD EA, 1992, GABAERGIC SYNAPTIC T, P17
[4]   NEUROSTEROIDS - A NEW FUNCTION IN THE BRAIN [J].
BAULIEU, EE .
BIOLOGY OF THE CELL, 1991, 71 (1-2) :3-10
[5]   THE GABA HYPOTHESIS OF KINDLING - RECENT ASSAY STUDIES [J].
BURNHAM, WM .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1989, 13 (04) :281-288
[6]  
BURNHAM WM, 1990, KINDLING, V4, P127
[7]  
BURNHAM WM, 1988, RECEPTORS LIGANDS NE, P171
[8]   LIDOCAINE BINDS WITH HIGH-AFFINITY TO PERIPHERAL-TYPE BENZODIAZEPINE RECEPTORS [J].
CLARK, M ;
POST, RM .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 179 (03) :473-475
[9]   EFFECT OF AMYGDALA KINDLING ON THE INVIVO RELEASE OF GABA AND 5-HT IN THE DORSAL RAPHE NUCLEUS IN FREELY MOVING RATS [J].
DURING, MJ ;
CRAIG, JS ;
HERNANDEZ, TD ;
ANDERSON, GM ;
GALLAGER, DW .
BRAIN RESEARCH, 1992, 584 (1-2) :36-44
[10]  
EDGAR PP, 1990, J NEUROSCI, V10, P603