Neural plasticity and stress induced changes in defense in the rat

被引:74
作者
Adamec, RE [1 ]
Blundell, J [1 ]
Collins, A [1 ]
机构
[1] Mem Univ Newfoundland, Dept Psychol, St John, NF A1B 3X9, Canada
基金
加拿大健康研究院;
关键词
amygdala; anxiety; evoked potentials; hippocampus; periaqueductal gray; plus maze; predator stress; startle;
D O I
10.1016/S0149-7634(01)00053-7
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
We investigated the effects of predator stress on behavior and amygdala afferent and efferent neural transmission in rats. Pathways studied were: ventral angular bundle input to the basolateral amygdala; central and basolateral amygdala output to the periaqueductal gray (PAG). Predator stress was 'anxiogenic' in elevated plus maze, light/dark box and acoustic startle tests one week after stress. Lasting changes were also observed in neural transmission. Predator stress appeared to potentiate right and depotentiate left hemisphere afferent amygdala transmission. In contrast, predator stress potentiated amygdala efferent transmission to right and left PAG, depending on the amygdala nucleus stimulated. Paired pulse and intensity series analysis suggests that transmission changes may be postsynaptic or presynaptic, depending on the pathway. Path analysis relating brain and behavioral changes suggests that potentiation and depotentiation in both hemispheres participate jointly in effecting some, but not all, of the behavioral changes produced by predator stress. Potentiation in left hemisphere amygdala afferents and efferents predicts anxiolytic-like effects, while potentiation in the right hemisphere amygdala afferents predicts anxiogenic-like effects. Path analysis also supports the view that changes in different neural systems mediate changes in different behaviors. These findings have their parallel in studies in the cat, but there are species differences. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:721 / 744
页数:24
相关论文
共 80 条
[31]   NMDA-coupled periaqueductal gray glycine receptors modulate anxioselective drug effects on plus-maze performance [J].
De Souza, MM ;
Schenberg, LC ;
Carobrez, ADP .
BEHAVIOURAL BRAIN RESEARCH, 1998, 90 (02) :157-165
[32]  
Dittman JS, 1997, J NEUROSCI, V17, P9048
[33]  
DOROW R, 1983, LANCET, V2, P98
[34]   TRIAL 2 IN THE ELEVATED PLUS-MAZE - A DIFFERENT FORM OF FEAR [J].
FILE, SE ;
ZANGROSSI, H ;
VIANA, M ;
GRAEFF, FG .
PSYCHOPHARMACOLOGY, 1993, 111 (04) :491-494
[35]   RELIABILITY OF HOLE-BOARD APPARATUS [J].
FILE, SE ;
WARDILL, AG .
PSYCHOPHARMACOLOGIA, 1975, 44 (01) :47-51
[36]   VALIDITY OF HEAD-DIPPING AS A MEASURE OF EXPLORATION IN A MODIFIED HOLE-BOARD [J].
FILE, SE ;
WARDILL, AG .
PSYCHOPHARMACOLOGIA, 1975, 44 (01) :53-59
[37]   STRUCTURAL SYNAPTIC CORRELATE OF LONG-TERM POTENTIATION - FORMATION OF AXOSPINOUS SYNAPSES WITH MULTIPLE, COMPLETELY PARTITIONED TRANSMISSION ZONES [J].
GEINISMAN, Y ;
DETOLEDOMORRELL, L ;
MORRELL, F ;
HELLER, RE ;
ROSSI, M ;
PARSHALL, RF .
HIPPOCAMPUS, 1993, 3 (04) :435-446
[38]  
Geinisman Y, 1996, J COMP NEUROL, V368, P413
[39]  
Gomez TMD, 1996, NEUROSCI LETT, V214, P5
[40]   AN ELECTROPHYSIOLOGICAL CHARACTERIZATION OF THE PROJECTION FROM THE CENTRAL NUCLEUS OF THE AMYGDALA TO THE PERIAQUEDUCTAL GRAY OF THE RAT - THE ROLE OF OPIOID RECEPTORS [J].
GOMEZ, TMD ;
BEHBEHANI, MM .
BRAIN RESEARCH, 1995, 689 (01) :21-31