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Single Neurons in the Monkey Hippocampus and Learning of New Associations
Sylvia Wirth,1Marianna Yanike,1Loren M. Frank,2Anne C. Smith,2Emery N. Brown,2Wendy A. Suzuki1*
The medial temporal lobe is crucial for the ability to learnand retain new declarative memories. This form of memory includesthe ability to quickly establish novel associations betweenunrelated items. To better understand the patterns of neuralactivity during associative memory formation, we recorded theactivity of hippocampal neurons of macaque monkeys as they learnednew associations. Hippocampal neurons signaled learning by changingtheir stimulus-selective response properties. This change inthe pattern of selective neural activity occurred before, atthe same time as, or after learning, which suggests that theseneurons are involved in the initial formation of new associativememories.
1 Center for Neural Science, New York University, New York, NY 10003, USA. 2 Harvard Medical School/MIT Division of Health, Sciences and Technology, Massachusetts General Hospital, Department of Anesthesia and Critical Care, Boston, MA 02114, USA.
* To whom correspondence should be addressed. E-mail: wendy{at}cns.nyu.edu
Characterizing Learning by Simultaneous Analysis of Continuous and Binary Measures of Performance.
M. J. Prerau, A. C. Smith, U. T. Eden, Y. Kubota, M. Yanike, W. Suzuki, A. M. Graybiel, and E. N. Brown (2009)
J Neurophysiol
102, 3060-3072
|Abstract »|Full Text »|PDF »
Robust Conjunctive Item-Place Coding by Hippocampal Neurons Parallels Learning What Happens Where.
R. W. Komorowski, J. R. Manns, and H. Eichenbaum (2009)
J. Neurosci.
29, 9918-9929
|Abstract »|Full Text »|PDF »
Context-Dependent Place-Selective Responses of the Neurons in the Medial Parietal Region of Macaque Monkeys.
Neuronal Activity in the Primary Somatosensory Thalamocortical Loop Is Modulated by Reward Contingency during Tactile Discrimination.
J. Pantoja, S. Ribeiro, M. Wiest, E. Soares, D. Gervasoni, N. A. M. Lemos, and M. A. L. Nicolelis (2007)
J. Neurosci.
27, 10608-10620
|Abstract »|Full Text »|PDF »
EEG Sharp Waves and Sparse Ensemble Unit Activity in the Macaque Hippocampus.
W. E. Skaggs, B. L. McNaughton, M. Permenter, M. Archibeque, J. Vogt, D. G. Amaral, and C. A. Barnes (2007)
J Neurophysiol
98, 898-910
|Abstract »|Full Text »|PDF »
Schemas and Memory Consolidation.
D. Tse, R. F. Langston, M. Kakeyama, I. Bethus, P. A. Spooner, E. R. Wood, M. P. Witter, and R. G. M. Morris (2007)
Science
316, 76-82
|Abstract »|Full Text »|PDF »
Neural encoding of the concept of nest in the mouse brain.
L. Lin, G. Chen, H. Kuang, D. Wang, and J. Z. Tsien (2007)
PNAS
104, 6066-6071
|Abstract »|Full Text »|PDF »
Bayesian Analysis of Interleaved Learning and Response Bias in Behavioral Experiments.
A. C. Smith, S. Wirth, W. A. Suzuki, and E. N. Brown (2007)
J Neurophysiol
97, 2516-2524
|Abstract »|Full Text »|PDF »
Homeostatic shutdown of long-term potentiation in the adult hippocampus.
C. Roth-Alpermann, R. G. M. Morris, M. Korte, and T. Bonhoeffer (2006)
PNAS
103, 11039-11044
|Abstract »|Full Text »|PDF »
Functional Magnetic Resonance Imaging Activity during the Gradual Acquisition and Expression of Paired-Associate Memory.
J. R. Law, M. A. Flanery, S. Wirth, M. Yanike, A. C. Smith, L. M. Frank, W. A. Suzuki, E. N. Brown, and C. E. L. Stark (2005)
J. Neurosci.
25, 5720-5729
|Abstract »|Full Text »|PDF »
Behavioral and Neurophysiological Analyses of Dynamic Learning Processes.
W. A. Suzuki and E. N. Brown (2005)
Behav Cogn Neurosci Rev
4, 67-95
|Abstract »|PDF »
Identification of network-level coding units for real-time representation of episodic experiences in the hippocampus.
L. Lin, R. Osan, S. Shoham, W. Jin, W. Zuo, and J. Z. Tsien (2005)
PNAS
102, 6125-6130
|Abstract »|Full Text »|PDF »
Analysis and Design of Behavioral Experiments to Characterize Population Learning.
A. C. Smith, M. R. Stefani, B. Moghaddam, and E. N. Brown (2005)
J Neurophysiol
93, 1776-1792
|Abstract »|Full Text »|PDF »
Sequential-Context-Dependent Hippocampal Activity Is Not Necessary to Learn Sequences with Repeated Elements.
M. R. Bower, D. R. Euston, and B. L. McNaughton (2005)
J. Neurosci.
25, 1313-1323
|Abstract »|Full Text »|PDF »
Cognitive Memory: Cellular and Network Machineries and Their Top-Down Control.
Hippocampal Plasticity across Multiple Days of Exposure to Novel Environments.
L. M. Frank, G. B. Stanley, and E. N. Brown (2004)
J. Neurosci.
24, 7681-7689
|Abstract »|Full Text »|PDF »
Spatial Representation in the Entorhinal Cortex.
M. Fyhn, S. Molden, M. P. Witter, E. I. Moser, and M.-B. Moser (2004)
Science
305, 1258-1264
|Abstract »|Full Text »|PDF »
Plasticity and tuning of the time course of analog persistent firing in a neural integrator.
G. Major, R. Baker, E. Aksay, H. S. Seung, and D. W. Tank (2004)
PNAS
101, 7745-7750
|Abstract »|Full Text »|PDF »
Inferior Temporal, Prefrontal, and Hippocampal Contributions to Visual Working Memory Maintenance and Associative Memory Retrieval.
C. Ranganath, M. X. Cohen, C. Dam, and M. D'Esposito (2004)
J. Neurosci.
24, 3917-3925
|Abstract »|Full Text »|PDF »
Categorization in the monkey hippocampus: A possible mechanism for encoding information into memory.
R. E. Hampson, T. P. Pons, T. R. Stanford, and S. A. Deadwyler (2004)
PNAS
101, 3184-3189
|Abstract »|Full Text »|PDF »
Dynamic Analysis of Learning in Behavioral Experiments.
A. C. Smith, L. M. Frank, S. Wirth, M. Yanike, D. Hu, Y. Kubota, A. M. Graybiel, W. A. Suzuki, and E. N. Brown (2004)
J. Neurosci.
24, 447-461
|Abstract »|Full Text »|PDF »