Despite the widespread appreciation that the medial temporal lobe (MTL) is necessary for episodic associative memory formation and retrieval, there is a fundamental gap in understanding the post-encoding processes by which memories are consolidate, or stabilized. This gap in knowledge is a critical problem because a host of psychiatric and neurologic disorders stem from a primary dysfunction of the MTL and how it contributes to associative memory. The long-term goal is to understand the mechanisms that support memory consolidation and what consequences these changes have on the integration of our new memories with past experience. The objective of the current proposal is to test a model of how post-encoding reactivation within MTL substructures known to be involved in encoding different aspects of an experience relate to the consolidation of those experiences. The central aim of the project is to establish reactivation as a mechanism for human episodic memory consolidation and to reveal distinct patterns of reactivation related to distinct kinds of memories. The rationale for the proposed research is that a better understanding of how the memories become stabilized over time will lead to a strong theoretical framework within which strategies for the understanding of mental disease disrupting memory will develop. The objective will be to identify, modulate and look for long-term consequences of reactivation which will be accomplished by pursuing three specific aims: 1) identify post-encoding patterns of reactivation that characterize recent prior experiences and relate to later associative memory for memories of different content;2) modulate post-encoding reactivation by linking reactivation with the amount of prior learning and hippocampal activity;and 3) linking post-encoding reactivation with longer-term changes in the memory representations. Strong preliminary data demonstrate the feasibility of project aims in the applicant's hands.
Under aim 1, evidence for reactivation of specific encoding experiences has been identified within the human hippocampus and evidence for distinct MTL interactions following encoding tasks presenting different memoranda.
Under aim 2, preliminary data provide evidence that the magnitude of hippocampal activation during encoding correlates with post-encoding hippocampal-cortical interactions.
Under aim 3, preliminary data identify expected patterns of change in the network representation of associative memories during reactivation that relate to behavioral measures of associative memory strength thus providing a much needed link between memory consolidation changes in the brain and strengthening of memories behaviorally. The approach is innovative and significant because we know very little about how interactions between MTL regions contribute to memory consolidation;it is highly programmatic because it is directly-motivated from our prior work on the role of MTL subregions to memory encoding and uses novel approaches to studying consolidation by looking for patterns of reactivation during post-encoding rest.

Public Health Relevance

The proposed research is relevant to public health because advancement in our understanding of the mechanisms by which memories consolidate in the normal brain is necessary to illuminate the mechanisms that could go awry in diseases that compromise the medial temporal lobes such as Alzheimer's disease. Specifically, the proposed research is relevant to NIH's mission because is expected to advance translational knowledge by providing empirical support in humans for processes identified in animals models and, thus, to strengthen theories of memory consolidation within which clinical researchers can develop strategies for the diagnosis and treatment of psychiatric and neurologic disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
2R01MH074692-06
Application #
8206105
Study Section
Special Emphasis Panel (ZRG1-IFCN-T (02))
Program Officer
Osborn, Bettina D
Project Start
2005-06-01
Project End
2016-12-31
Budget Start
2012-02-24
Budget End
2012-12-31
Support Year
6
Fiscal Year
2012
Total Cost
$374,120
Indirect Cost
$124,120
Name
New York University
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
041968306
City
New York
State
NY
Country
United States
Zip Code
10012
Duncan, Katherine; Tompary, Alexa; Davachi, Lila (2014) Associative encoding and retrieval are predicted by functional connectivity in distinct hippocampal area CA1 pathways. J Neurosci 34:11188-98
DuBrow, Sarah; Davachi, Lila (2014) Temporal memory is shaped by encoding stability and intervening item reactivation. J Neurosci 34:13998-4005
Ezzyat, Youssef; Davachi, Lila (2014) Similarity breeds proximity: pattern similarity within and across contexts is related to later mnemonic judgments of temporal proximity. Neuron 81:1179-89
Markant, Douglas; DuBrow, Sarah; Davachi, Lila et al. (2014) Deconstructing the effect of self-directed study on episodic memory. Mem Cognit 42:1211-24
Tambini, Arielle; Davachi, Lila (2013) Persistence of hippocampal multivoxel patterns into postencoding rest is related to memory. Proc Natl Acad Sci U S A 110:19591-6
Heusser, Andrew C; Awipi, Tarimotimi; Davachi, Lila (2013) The ups and downs of repetition: modulation of the perirhinal cortex by conceptual repetition predicts priming and long-term memory. Neuropsychologia 51:2333-43
Vilberg, Kaia L; Davachi, Lila (2013) Perirhinal-hippocampal connectivity during reactivation is a marker for object-based memory consolidation. Neuron 79:1232-42
DuBrow, Sarah; Davachi, Lila (2013) The influence of context boundaries on memory for the sequential order of events. J Exp Psychol Gen 142:1277-86
Duncan, Katherine; Ketz, Nicholas; Inati, Souheil J et al. (2012) Evidence for area CA1 as a match/mismatch detector: a high-resolution fMRI study of the human hippocampus. Hippocampus 22:389-98
Tubridy, Shannon; Davachi, Lila (2011) Medial temporal lobe contributions to episodic sequence encoding. Cereb Cortex 21:272-80

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