Behavioral characterization of pentylenetetrazol-induced seizures in the marmoset

被引:25
作者
Bachiega, Joao C. [1 ]
Blanco, Miriam M. [1 ]
Perez-Mendes, Patricia [1 ]
Cinini, Simone Maria [1 ]
Covolan, Luciene [1 ]
Mello, Luiz E. [1 ]
机构
[1] Univ Fed Sao Paulo, Dept Physiol, BR-04023062 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
marmoset; pentylenetetrazol; antiepileptic drugs; epilepsy model;
D O I
10.1016/j.yebeh.2008.02.010
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
This study was designed to characterize seizures induced with pentylenetetrazol (PTZ) in marmosets. Thirteen adult marmosets (Callithrix sp.) received 20, 30, or 40 mg/kg of PTZ intraperitoneally. PTZ caused all animals to switch their natural behavioral repertoire to early convulsive behavior. Seizure scores were low at lower PTZ doses, whereas the highest dose of PTZ led to seizure scores IV and V (according to Racine's scale) in 69% of animals. To further characterize the model we performed a preliminary evaluation of the efficacy of three antiepileptic drugs: phenobarbital, phenytoin, and carbamazepine. Phenobarbital prevented PTZ-induced seizures in 100% of trials. As expected, phenytoin and carbamazepine were not effective against PTZ-induced seizures. The present study describes the PTZ model of seizures in marmosets with a drug-response profile similar to that of the rodent model, thus bringing to a well-known model (PTZ in rodents) the complexity of a nonhuman primate brain. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:70 / 76
页数:7
相关论文
共 43 条
[1]   THE DIFFERENTIAL ACTIVITIES OF R(+)-ZACOPRIDE AND S(-)-ZACOPRIDE AS 5-HT3 RECEPTOR ANTAGONISTS [J].
BARNES, JM ;
BARNES, NM ;
COSTALL, B ;
DOMENEY, AM ;
JOHNSON, DN ;
KELLY, ME ;
MUNSON, HR ;
NAYLOR, RJ ;
YOUNG, R .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1990, 37 (04) :717-727
[2]   Measuring fear and anxiety in the marmoset (Callithrix penicillata) with a novel predator confrontation model:: effects of diazepam [J].
Barros, M ;
Boere, V ;
Huston, JP ;
Tomaz, C .
BEHAVIOURAL BRAIN RESEARCH, 2000, 108 (02) :205-211
[3]   Non-human primate models for investigating fear and anxiety [J].
Barros, M ;
Tomaz, C .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2002, 26 (02) :187-201
[4]   THE ROLE OF EPILEPTIC ACTIVITY IN HIPPOCAMPAL AND REMOTE CEREBRAL-LESIONS INDUCED BY KAINIC ACID [J].
BENARI, Y ;
TREMBLAY, E ;
OTTERSEN, OP ;
MELDRUM, BS .
BRAIN RESEARCH, 1980, 191 (01) :79-97
[5]  
BLANCO MM, 2005, NOVAS ESTRATEGIAS AB
[6]   Isobolographic and subthreshold analysis of interactions among felbamate and four conventional antiepileptic drugs in pentylenetetrazole-induced seizures in mice [J].
Borowicz, KK ;
Luszczki, JJ ;
Czuczwar, TJ .
EPILEPSIA, 2004, 45 (10) :1176-1183
[7]  
BURLEY ES, 1984, FED PROC, V43, P2521
[8]   ANTICONVULSANT ACTIVITY OF 2 ORALLY ACTIVE COMPETITIVE N-METHYL-D-ASPARTATE ANTAGONISTS, CGP 37849 AND CGP 39551, AGAINST SOUND-INDUCED SEIZURES IN DBA/2 MICE AND PHOTICALLY INDUCED MYOCLONUS IN PAPIO-PAPIO [J].
CHAPMAN, AG ;
GRAHAM, JL ;
PATEL, S ;
MELDRUM, BS .
EPILEPSIA, 1991, 32 (04) :578-587
[9]   Marmoset conspecific confrontation: An ethologically-based model of anxiety [J].
Cilia, J ;
Piper, DC .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1997, 58 (01) :85-91
[10]  
COSTALL B, 1992, J PHARMACOL EXP THER, V262, P90