Hippocampal Lesions Impair Rapid Learning of a Continuous Spatial Alternation Task

被引:53
作者
Kim, Steve M.
Frank, Loren M.
机构
[1] Neuroscience Graduate Program, University of California San Francisco, San Francisco, CA
[2] Department of Physiology, University of California San Francisco, San Francisco, CA
[3] W.M. Keck Foundation Center for Integrative Neuroscience, University of California San Francisco, San Francisco, CA
来源
PLOS ONE | 2009年 / 4卷 / 05期
关键词
D O I
10.1371/journal.pone.0005494
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The hippocampus is essential for the formation of memories for events, but the specific features of hippocampal neural activity that support memory formation are not yet understood. The ideal experiment to explore this issue would be to monitor changes in hippocampal neural coding throughout the entire learning process, as subjects acquire and use new episodic memories to guide behavior. Unfortunately, it is not clear whether established hippocampally-dependent learning paradigms are suitable for this kind of experiment. The goal of this study was to determine whether learning of the W-track continuous alternation task depends on the hippocampal formation. We tested six rats with NMDA lesions of the hippocampal formation and four sham-operated controls. Compared to controls, rats with hippocampal lesions made a significantly higher proportion of errors and took significantly longer to reach learning criterion. The effect of hippocampal lesion was not due to a deficit in locomotion or motivation, because rats with hippocampal lesions ran well on a linear track for food reward. Rats with hippocampal lesions also exhibited a pattern of perseverative errors during early task experience suggestive of an inability to suppress behaviors learned during pretraining on a linear track. Our findings establish the W-track continuous alternation task as a hippocampally-dependent learning paradigm which may be useful for identifying changes in the neural representation of spatial sequences and reward contingencies as rats learn and apply new task rules.
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页数:13
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[41]   Hippocampus lesions impair landmark array spatial learning in homing pigeons: A laboratory study [J].
White, AR ;
Strasser, R ;
Bingman, VP .
NEUROBIOLOGY OF LEARNING AND MEMORY, 2002, 78 (01) :65-78
[42]   Spatial and visual alternation learning in pigeons [J].
Hiraoka, Kyoichi .
INTERNATIONAL JOURNAL OF PSYCHOLOGY, 2016, 51 :829-830
[43]   COMBINED EFFECTS OF REM SLEEP DEPRIVATION AND HIPPOCAMPAL FIMBRIA-FORNIX TRANSECTIONS OR LESIONS ON ABILITY TO ACQUIRE A SPATIAL LEARNING TASK [J].
Poe, G. R. ;
Pal, D. ;
Roberson, T. ;
Biswas, S. .
SLEEP, 2009, 32 :A163-A163
[44]   SELECTIVE FIMBRIA LESIONS IMPAIR ACQUISITION OF WORKING AND REFERENCE MEMORY OF RATS IN A COMPLEX SPATIAL DISCRIMINATION TASK [J].
VANDERSTAAY, FJ ;
RAAIJMAKERS, WGM ;
LAMMERS, AJJC ;
TONNAER, JADM .
BEHAVIOURAL BRAIN RESEARCH, 1989, 32 (02) :151-161
[45]   Lesions Affecting the Right Hippocampal Formation Differentially Impair Short-Term Memory of Spatial and Nonspatial Associations [J].
Braun, Mischa ;
Weinrich, Christiane ;
Finke, Carsten ;
Ostendorf, Florian ;
Lehmann, Thomas-Nicolas ;
Ploner, Christoph J. .
HIPPOCAMPUS, 2011, 21 (03) :309-318
[46]   Hippocampal lesions impair memory for location but not color in passerine birds [J].
Hampton, RR ;
Shettleworth, SJ .
BEHAVIORAL NEUROSCIENCE, 1996, 110 (04) :831-835
[47]   A new continuous alternation task in T-maze detects hippocampal dysfunction in mice - A strain comparison and lesion study [J].
Gerlai, R .
BEHAVIOURAL BRAIN RESEARCH, 1998, 95 (01) :91-101
[48]   IMPACT OF TEMPORAL LOBE SPIKES ON HIPPOCAMPAL REPLAY DURING AN ALTERNATION TASK [J].
Richard, Gregory ;
Santini, P. P. ;
Kleen, J. K. ;
Holmes, G. L. .
EPILEPSIA, 2009, 50 :296-297
[49]   DORSAL HIPPOCAMPAL-LESIONS IMPAIR BLOCKING BUT NOT LATENT INHIBITION OF TASTE-AVERSION LEARNING IN RATS [J].
GALLO, M ;
CANDIDO, A .
BEHAVIORAL NEUROSCIENCE, 1995, 109 (03) :413-425
[50]   Cerebellar lesions impair rapid saccade amplitude adaptation [J].
Straube, A ;
Deubel, H ;
Ditterich, J ;
Eggert, T .
NEUROLOGY, 2001, 57 (11) :2105-2108