Our previous study successfully identified the relationship between activity in the hippocampus and the medial prefrontal cortex during active choice behavior in a spatial working memory task in which prefrontal neurons became phase-locked to the hippocampal theta rhythm and tightly correlated with hippocampal place cells prior to accurate choice responses. Our studies also identified a novel form of hippocampal activity during quiet wakefulness in which sequential place cell activity reflecting past behavior was reactivated during stopping at goal locations. Preliminary results have provided further evidence of reactivation of forward sequences reflecting future trajectories during stopping at non-goal locations. Together these findings suggest that interactions between the hippocampus and prefrontal cortex during both active behavior and periods of awake inactivity may contribute to learning of behavioral contingencies in choice tasks through both prospective evaluation of future states, and retrospective evaluation of past states, and that these interactions may serve as a general biological substrate for unsupervised reinforcement learning. The possible contribution of these events to reinforcement learning would further suggest the involvement of reinforcement related activity in areas known to express correlates of reward and expectation of reward such as the ventral tegmental area (VTA). The present proposal seeks to further elaborate the relationship between the structure of neuronal activity, and behavioral events involved in learning of simple reinforced spatial working memory tasks by conducting simultaneous multielectrode recording of neuronal ensembles at multiple sites within the medial prefrontal cortex area (RFC), the ventral tegmental area (VTA), and the CA1 region of the hippocampus during active behavior, awake inactivity, and during sleep.
These aims will extend the basic relationship between behavioral correlates of PFC activity established in previous work to the newly discovered phenomena of forward and reverse hippocampal sequence memory reactivation during quiet wakefulness, and will identify novel correlates of reinforcement-related activity in the VTA and their relationship to activity in both the hippocampus and PFC as they may relate to the general process of reinforcement learning. Given the known involvement of these brain areas in a broad spectrum of cognitive functions and behavioral and neuropsychiatric disorders, including spatial navigation, memory encoding and retrieval, addiction, schizophrenia, autism, and attention deficit disorders, this study will provide important insights into basic mechanisms that may contribute to learning, memory, and cognition, and establish novel biological substrates for computational models of neural function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH061976-08
Application #
7647194
Study Section
Neurobiology of Learning and Memory Study Section (LAM)
Program Officer
Osborn, Bettina D
Project Start
2000-07-01
Project End
2012-06-30
Budget Start
2009-07-01
Budget End
2010-06-30
Support Year
8
Fiscal Year
2009
Total Cost
$378,000
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Miscellaneous
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Sanders, Honi; Ji, Daoyun; Sasaki, Takuya et al. (2018) Temporal coding and rate remapping: Representation of nonspatial information in the hippocampus. Hippocampus :
Linderman, Scott W; Johnson, Matthew J; Wilson, Matthew A et al. (2016) A Bayesian nonparametric approach for uncovering rat hippocampal population codes during spatial navigation. J Neurosci Methods 263:36-47
Gomperts, Stephen N; Kloosterman, Fabian; Wilson, Matthew A (2015) VTA neurons coordinate with the hippocampal reactivation of spatial experience. Elife 4:
Remondes, Miguel; Wilson, Matthew A (2015) Slow-? Rhythms Coordinate Cingulate Cortical Responses to Hippocampal Sharp-Wave Ripples during Wakefulness. Cell Rep 13:1327-1335
Wilson, Matthew A; Varela, Carmen; Remondes, Miguel (2015) Phase organization of network computations. Curr Opin Neurobiol 31:250-3
Flores, Francisco J; Ching, ShiNung; Hartnack, Katharine et al. (2015) A PK-PD model of ketamine-induced high-frequency oscillations. J Neural Eng 12:056006
Halassa, Michael M; Chen, Zhe; Wimmer, Ralf D et al. (2014) State-dependent architecture of thalamic reticular subnetworks. Cell 158:808-821
Kloosterman, Fabian; Layton, Stuart P; Chen, Zhe et al. (2014) Bayesian decoding using unsorted spikes in the rat hippocampus. J Neurophysiol 111:217-27
Varela, C; Kumar, S; Yang, J Y et al. (2014) Anatomical substrates for direct interactions between hippocampus, medial prefrontal cortex, and the thalamic nucleus reuniens. Brain Struct Funct 219:911-29
Chen, Zhe; Gomperts, Stephen N; Yamamoto, Jun et al. (2014) Neural representation of spatial topology in the rodent hippocampus. Neural Comput 26:1-39

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