INCREASED PHASIC DOPAMINE SIGNALING IN THE MESOLIMBIC PATHWAY DURING SOCIAL DEFEAT IN RATS

被引:186
作者
Anstrom, K. K. [1 ]
Miczek, K. A. [2 ,3 ,4 ,5 ]
Budygin, E. A. [1 ]
机构
[1] Wake Forest Univ Hlth Sci, Dept Physiol & Pharmacol, Winston Salem, NC 27157 USA
[2] Tufts Univ, Dept Psychol, Medford, MA 02155 USA
[3] Tufts Univ, Dept Psychiat, Medford, MA 02155 USA
[4] Tufts Univ, Dept Pharmacol, Medford, MA 02155 USA
[5] Tufts Univ, Dept Neurosci, Medford, MA 02155 USA
基金
美国国家卫生研究院;
关键词
social defeat; stress; voltammetry; electrophysiology; dopamine; VENTRAL TEGMENTAL AREA; SCAN CYCLIC VOLTAMMETRY; FREELY MOVING RATS; NUCLEUS-ACCUMBENS; NEURONAL-ACTIVITY; AFFERENT MODULATION; SUBSTANTIA-NIGRA; FIRING PATTERN; BEHAVING RATS; BASAL GANGLIA;
D O I
10.1016/j.neuroscience.2009.03.023
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
While reward-dependent facilitation of phasic dopamine signaling is well documented at both the cell bodies and terminals, little is known regarding fast dopamine transmission under aversive conditions. Exposure to aggressive confrontation is extremely aversive and stressful for many species including rats. The present study used fast-scan cyclic voltammetry and multiunit recording to determine if aggressive encounters and subsequent social defeat affect burst firing of ventral tegmental area (VTA) dopamine neurons and accumbal dopamine transients in defeated rats. Significant increases in the frequency of transient dopamine release were observed during interactions with an aggressive rat but not with a familiar cage mate. In agreement with voltammetric results, significant increases in burst frequency were detected in the VTA dopamine firing patterns during an aggressive confrontation; however, the number of spikes per burst remained unchanged. We found that neurons with lower burst rates under home cage conditions did not switch from nonbursting to bursting types, while neurons with higher burst levels showed amplified increases in bursting. This study demonstrates for the first time that aggressive confrontations in defeated rats are associated with increases in phasic dopamine transmission in the mesolimbic pathway. (C) 2009 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3 / 12
页数:10
相关论文
共 70 条
[1]  
ALDRIDGE JW, 1991, BRAIN RES, V543, P123
[2]  
[Anonymous], 2005, The Behavior of the Laboratory Rat: A Handbook with Tests, DOI DOI 10.1093/ACPROF:OSO/9780195162851.001.0001
[3]   Effects of restraint and haloperidol on sensory gating in the midbrain of awake rats [J].
Anstrom, K. K. ;
Cromwell, H. C. ;
Woodward, D. J. .
NEUROSCIENCE, 2007, 146 (02) :515-524
[4]   Restraint increases dopaminergic burst firing in awake rats [J].
Anstrom, KK ;
Woodward, DJ .
NEUROPSYCHOPHARMACOLOGY, 2005, 30 (10) :1832-1840
[5]   The effects of predator odors in mammalian prey species: A review of field and laboratory studies [J].
Apfelbach, R ;
Blanchard, CD ;
Blanchard, RJ ;
Hayes, RA ;
McGregor, IS .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2005, 29 (08) :1123-1144
[6]   The debate over dopamine's role in reward: the case for incentive salience [J].
Berridge, Kent C. .
PSYCHOPHARMACOLOGY, 2007, 191 (03) :391-431
[7]   Correlation between behavior and extracellular dopamine levels in rat striatum: comparison of microdialysis and fast-scan cyclic voltammetry [J].
Budygin, EA ;
Kilpatrick, MR ;
Gainetdinov, RR ;
Wightman, RM .
NEUROSCIENCE LETTERS, 2000, 281 (01) :9-12
[8]   Dopamine uptake inhibition is positively correlated with cocaine-induced stereotyped behavior [J].
Budygin, Evgeny A. .
NEUROSCIENCE LETTERS, 2007, 429 (01) :55-58
[9]   ELECTROPHYSIOLOGICAL AND PHARMACOLOGICAL EVIDENCE FOR THE ROLE OF THE NUCLEUS-ACCUMBENS IN COCAINE SELF-ADMINISTRATION IN FREELY MOVING RATS [J].
CHANG, JY ;
SAWYER, SF ;
LEE, RS ;
WOODWARD, DJ .
JOURNAL OF NEUROSCIENCE, 1994, 14 (03) :1224-1244
[10]   Coordinated accumbal dopamine release and neural activity drive goal-directed behavior [J].
Cheer, Joseph F. ;
Aragona, Brandon J. ;
Heien, Michael L. A. V. ;
Seipel, Andrew T. ;
Carelli, Regina M. ;
Wightman, R. Mark .
NEURON, 2007, 54 (02) :237-244