Rats with different thresholds for DMCM-induced clonic convulsions differ in the sleep-time of diazepam and [3H]-Ro 15-4513 binding

被引:2
作者
Conto, Marcos Brandao [1 ]
Hipolide, Debora Cristina [1 ]
Barbosa de Carvalho, Jose Gilberto [1 ]
Campana Venditti, Marco Antonio [1 ]
机构
[1] Univ Fed Sao Paulo, Escola Paulista Med UNIFESP EPM, Dept Psicobiol, BR-04023900 Sao Paulo, Brazil
关键词
H-3]-flunitrazepam; H-3]-Ro 15-4513; DMCM; GABA(A); Convulsions; Sleeping time; BENZODIAZEPINE INVERSE AGONIST; ELEVATED PLUS-MAZE; GABA(A) RECEPTOR; BEHAVIORAL-DIFFERENCES; EPILEPSY; ETHANOL; BRAIN; PHARMACOLOGY; WAKEFULNESS; SENSITIVITY;
D O I
10.1016/j.eplepsyres.2011.09.014
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The current study investigated the possible inherent relationship between convulsions and sleep involving the GABA(A)/benzodiazepine site complex. The aim of this study was to determine if rats with high (HTR) and low (LTR) thresholds for clonic convulsions induced by DMCM, a benzodiazepine inverse agonist, differ in the following aspects: (1) sensitivity to the hypnotic effects of the GABA(A) positive allosteric modulators diazepam, pentobarbital and ethanol and (2) in the binding of [H-3]-flunitrazepam, a benzodiazepine agonist, measured by autoradiography, and [H-3]-Ro 15-4513, a benzodiazepine partial inverse agonist, to membranes from discrete brain regions. The LTR subgroup presented a shorter diazepam-induced sleeping time compared to that of the HTR subgroup. Biochemical assays revealed that the LTR subgroup did not differ in [H-3]-flunitrazepam binding compared to the HTR subgroup. With respect to the binding of [H-3]-Ro 15-4513, the LTR subgroup had higher binding in the brainstem and lower binding in the striatum compared to the HTR subgroup. These results suggest that differences in the benzodiazepine site on the GABA(A) receptor may underlie the susceptibility to DMCM-induced convulsions and sensitivity to the hypnotic effect of diazepam. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:216 / 222
页数:7
相关论文
共 45 条
[31]   Psychiatric complications in patients with epilepsy: a review [J].
Marsh, L ;
Rao, V .
EPILEPSY RESEARCH, 2002, 49 (01) :11-33
[32]   An update on GABAA receptors [J].
Mehta, AK ;
Ticku, MK .
BRAIN RESEARCH REVIEWS, 1999, 29 (2-3) :196-217
[33]   CHRONIC ETHANOL ADMINISTRATION INCREASES THE BINDING OF THE BENZODIAZEPINE INVERSE AGONIST AND ALCOHOL ANTAGONIST [H-3] RO15-4513 IN RAT-BRAIN [J].
MHATRE, M ;
MEHTA, AK ;
TICKU, MK .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 153 (01) :141-145
[34]  
MHATRE M, 1989, J PHARMACOL EXP THER, V251, P164
[35]   A new benzodiazepine pharmacology [J].
Möhler, H ;
Fritschy, JM ;
Rudolph, U .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 300 (01) :2-8
[36]   Which seizure-precipitating factors do patients with epilepsy most frequently report? [J].
Nakken, KO ;
Solaas, MH ;
Kjeldsen, MJ ;
Friis, ML ;
Pellock, JM ;
Corey, LA .
EPILEPSY & BEHAVIOR, 2005, 6 (01) :85-89
[37]   ALTERATIONS IN THE BRAIN GABA(A)/BENZODIAZEPINE RECEPTOR CHLORIDE IONOPHORE COMPLEX IN A GENETIC MODEL OF PAROXYSMAL DYSTONIA - A QUANTITATIVE AUTORADIOGRAPHIC ANALYSIS [J].
NOBREGA, JN ;
RICHTER, A ;
BURNHAM, WM ;
LOSCHER, W .
NEUROSCIENCE, 1995, 64 (01) :229-239
[38]   New insights into the role of the GABAA-benzodiazepine receptor in psychiatric disorder [J].
Nutt, DJ ;
Malizia, AL .
BRITISH JOURNAL OF PSYCHIATRY, 2001, 179 :390-396
[39]   BENZODIAZEPINE-GAMMA-AMINOBUTYRIC ACID RECEPTOR DEFICIT IN THE MIDBRAIN OF THE SEIZURE-SUSCEPTIBLE GERBIL [J].
OLSEN, RW ;
WAMSLEY, JK ;
MCCABE, RT ;
LEE, RJ ;
LOMAX, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (19) :6701-6705
[40]  
Paxinos G., 1998, RAT BRAIN STEROTAXIC, VFourth