Interaction between midazolam-induced anterograde amnesia and memory enhancement by treatments given immediately after training on an inhibitory avoidance task in rats

被引:6
作者
Quevedo, J [1 ]
de-Paris, F
Vianna, MRM
Barichello, T
Roesler, R
Kapczinski, F
机构
[1] Univ Extremo Sul Catarinense, Lab Neurotoxicol, BR-88806000 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Inst Ciencias Basicas Saude, Dept Bioquim, Ctr Memoria, BR-90035003 Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Fac Med, Dept Psiquiatria, BR-90035003 Porto Alegre, RS, Brazil
[4] Univ Fed Rio Grande do Sul, Hosp Clin Porto Alegre, GrpPsicofarmacol, BR-90035003 Porto Alegre, RS, Brazil
来源
BEHAVIOURAL PHARMACOLOGY | 2002年 / 13卷 / 04期
关键词
midazolam; adrenaline; naloxone; dexamethasone; glucose; memory; inhibitory avoidance; rat;
D O I
10.1097/00008877-200207000-00009
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
The aim of this study was to evaluate the effects of interactions between memory modulatory systems on inhibitory avoidance retention in rats. Adult female Wistar rats were trained and tested in a step-down inhibitory avoidance task (0.3 mA footshock). The training-test interval was 24 h. The animals received an intraperitoneal injection of saline or midazolam (1 mg/kg) 15 min before training, and saline, adrenaline (25 mug/kg), naloxone (0.4 mg/kg), dexamethasone (0.3 mg/kg) or glucose (320 mg/kg) immediately after training. In saline-pretreated rats, adrenaline, naloxone, dexamethasone and glucose enhanced memory retention. Pretreatment with midazolam prevented the facilitatory effects of those treatments. These findings suggest that the facilitation of learning by post-training memory-enhancing treatments is prevented by midazolam. (C) 2002 Lippincott Williams Wilkins.
引用
收藏
页码:319 / 322
页数:4
相关论文
共 24 条
[1]  
Barros DM, 1998, BEHAV PHARMACOL, V9, P163
[2]  
BOHUS B, 1993, ANN NY ACAD SCI, V689, P285
[3]   Modulation of memory storage [J].
Cahill, L ;
McGaugh, JL .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (02) :237-242
[4]   OXOTREMORINE ATTENUATES RETROGRADE-AMNESIA INDUCED BY POST-TRAINING ADMINISTRATION OF THE GABAERGIC AGONISTS MUSCIMOL AND BACLOFEN [J].
CASTELLANO, C ;
MCGAUGH, JL .
BEHAVIORAL AND NEURAL BIOLOGY, 1991, 56 (01) :25-31
[5]  
CASTELLANO C, 1990, BIOL MEMORY, P175
[6]   BEHAVIORAL PHARMACOLOGY OF MINOR TRANQUILIZERS [J].
FILE, SE ;
PELLOW, S .
PHARMACOLOGY & THERAPEUTICS, 1987, 35 (03) :265-290
[7]  
GOLD PE, 1991, NEUR CONT B, V6, P391
[8]  
GOLD PE, 1994, BRAIN MEMORY MODULAT, P201
[9]   DIFFERENT FORMS OF POST-TRAINING MEMORY PROCESSING [J].
IZQUIERDO, I .
BEHAVIORAL AND NEURAL BIOLOGY, 1989, 51 (02) :171-202
[10]   DIAZEPAM PREVENTS POST-TRAINING DRUG EFFECTS RELATED TO STATE DEPENDENCY, BUT NOT POST-TRAINING MEMORY FACILITATION BY EPINEPHRINE [J].
IZQUIERDO, I ;
FERREIRA, MBC .
BEHAVIORAL AND NEURAL BIOLOGY, 1989, 51 (01) :73-79