Skip to main content
  • Poster presentation
  • Open access
  • Published:

A connectionist model of context-based memory reconsolidation in the hippocampus: the role of sleep

Context-based memory reconsolidation has been studied in human and animal models [1]. In these paradigms, subjects learn two lists of items on two different days and are asked to recall the first list on day 3. Subjects who learn the two lists in the same spatial context make significantly more errors on day 3 than subjects who learn the lists in different contexts. This result suggests that contextual information may be linked to item information during memory formation or consolidation, and that this link is responsible for intrusions of items from the second list into the first list during recall when the lists were learned in identical contexts. The neural mechanisms underlying this process are unknown, but experimental studies have suggested that the hippocampus may be critical.

Experimental work has shown that the dorsal and ventral portions of the hippocampus may implement qualitatively different functions in memory and spatial navigation [2], and that the proximal and distal portions of CA1 may carry information related to self-motion and sensory perception respectively [3]. We hypothesize that the dorso-ventral and proximal-distal anatomical differentiations of this structure may explain some of the experimental data on memory reconsolidation. To test this hypothesis, we built a connectionist model of the hippocampus (figure 1). The model is implemented using EMERGENT [4]. In this model, the dorsal stream carries predominantly item information, while the ventral stream carries spatial contextual information. In both streams, the distal CA1 encodes items using inputs from the lateral entorhinal cortex, while the proximal CA1 encodes spatial context using medial entorhinal cortical inputs. We train and test the model as in the experiments.

Figure 1
figure 1

Model architecture. Separate and interacting ‘object’ and ‘context’ streams shown in blue and red respectively, with explicit output ‘guesses’.

We found that object representation overlap as well as additional, extraneous learning can explain how context affects recall performance and produce intrusions as observed experimentally. We then selectively lesion the network to investigate which component of the hippocampus affects context based memory recall. In addition, we use the model to understand memory reactivation during sleep. Sleep is simulated by presenting small amounts of noise in the input layers. We found that this noise partially re-activated the memory representations of objects that were previously learned. These partial memories were then set as inputs and were re-processed by the network. This in turn made these memories resilient to interference from new items learned at a later time as was shown experimentally [5]. The model will allow for an investigation of why certain items have preferential memory reactivation during sleep. Furthermore, the model may be used to explain recent experimental data showing that presenting specific external stimuli during sleep may influence the memory consolidation process [6].

References

  1. Jones B, Bukoski E, Nadel L, Fellous JM: Remaking Memories: Reconsolidation Updates Positively Motivated Spatial Memory in Rats. Learn. Mem. 2012, 19: 91-98. 10.1101/lm.023408.111.

    Article  PubMed Central  PubMed  Google Scholar 

  2. Nadel L, Hoscheidt S, Ryan L: Spatial Cognition and the Hippocampus: The Anterior-Posterior Axis. J. Cognitive Neurosci. 2013, 25: 22-28. 10.1162/jocn_a_00313.

    Article  Google Scholar 

  3. Henriksen E, Colgin L, Barnes C, Witter M, Moser MB, Moser E: Spatial Representation Along the Proximodistal Axis of CA1. Neuron. 2010, 68: 127-137. 10.1016/j.neuron.2010.08.042.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  4. Aisa B, Mingus B, O’Reilly R: The Emergent Neural Modeling System. Neural Networks. 2008, 21: 1146-1152. 10.1016/j.neunet.2008.06.016.

    Article  PubMed  Google Scholar 

  5. Ellenbogen J, Hulbert J, Stickgold R, Dinges D, Thompson-Schill S: Interfering with Theories of Sleep and Memory: Sleep, Declarative Memory, and Associative Interference. Curr. Biol. 2006, 16: 1290-1294. 10.1016/j.cub.2006.05.024.

    Article  CAS  PubMed  Google Scholar 

  6. Rasch B, Büchel C, Gais S, Born J: Odor Cues During Slow-Wave Sleep Prompt Declarative Memory Consolidation. Science. 2007, 315: 1426-1429. 10.1126/science.1138581.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Justin Lines.

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Lines, J., Nation, K. & Fellous, JM. A connectionist model of context-based memory reconsolidation in the hippocampus: the role of sleep. BMC Neurosci 15 (Suppl 1), P163 (2014). https://doi.org/10.1186/1471-2202-15-S1-P163

Download citation

  • Published:

  • DOI: https://doi.org/10.1186/1471-2202-15-S1-P163

Keywords