Literature DB >> 23389924

The conjunctive trace.

Blake A Richards1, Paul W Frankland.   

Abstract

Memories serve to establish some permanence to our inner lives despite the fleeting nature of subjective experience. Most neurobiological theories of memory assume that this mental permanence reflects an underlying cellular permanence. Namely, it is assumed that the cellular changes which first occur to store a memory are perpetuated for as long as the memory is stored. But is that really the case? In an opinion piece in this issue of Hippocampus, Aryeh Routtenberg raises the provocative idea that the subjective sense of memory persistence is not in fact a result of persistence at the cellular level, rather, that "supple synapses" and multiple "evanescent networks" that are forever changing are responsible for our memories. On one level, his proposal could be construed as a radical challenge to some of our most fundamental theories of the neurobiology of memory, including Donald Hebb's proposal that memories are stored by networks that strengthen their connections to increase the likelihood of the same activity patterns being recreated at a later date. However, it could also be seen as a moderating call, a call for a greater acknowledgement of the dynamic, stochastic, and distributed nature of neural networks. In this response to Routtenberg's article, we attempt to provide a clarification of the dividing line between these two interpretations of his argument, and in doing so, we provide some overview of the empirical evidence that bears on this subject. We argue that the data that exists to date favors the more moderate interpretation: that memory storage involves a process in which activity patterns are made more likely to reoccur, but that an under-appreciated reality is that mnemonic traces may continue to change and evolve over time.
Copyright © 2013 Wiley Periodicals, Inc.

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Year:  2013        PMID: 23389924     DOI: 10.1002/hipo.22089

Source DB:  PubMed          Journal:  Hippocampus        ISSN: 1050-9631            Impact factor:   3.899


  8 in total

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Authors:  Sheena A Josselyn; Stefan Köhler; Paul W Frankland
Journal:  Nat Rev Neurosci       Date:  2015-09       Impact factor: 34.870

2.  Voluntary Running Exercise-Mediated Enhanced Neurogenesis Does Not Obliterate Retrograde Spatial Memory.

Authors:  Maheedhar Kodali; Tarick Megahed; Vikas Mishra; Bing Shuai; Bharathi Hattiangady; Ashok K Shetty
Journal:  J Neurosci       Date:  2016-08-03       Impact factor: 6.167

3.  Elevation of Hippocampal Neurogenesis Induces a Temporally Graded Pattern of Forgetting of Contextual Fear Memories.

Authors:  Aijing Gao; Frances Xia; Axel J Guskjolen; Adam I Ramsaran; Adam Santoro; Sheena A Josselyn; Paul W Frankland
Journal:  J Neurosci       Date:  2018-02-16       Impact factor: 6.167

4.  Digital computing through randomness and order in neural networks.

Authors:  Alexandre Pitti; Claudio Weidmann; Mathias Quoy
Journal:  Proc Natl Acad Sci U S A       Date:  2022-08-10       Impact factor: 12.779

Review 5.  Memory engrams: Recalling the past and imagining the future.

Authors:  Sheena A Josselyn; Susumu Tonegawa
Journal:  Science       Date:  2020-01-03       Impact factor: 47.728

Review 6.  The neurobiological foundation of memory retrieval.

Authors:  Paul W Frankland; Sheena A Josselyn; Stefan Köhler
Journal:  Nat Neurosci       Date:  2019-09-24       Impact factor: 24.884

Review 7.  Identification and optogenetic manipulation of memory engrams in the hippocampus.

Authors:  Steve Ramirez; Susumu Tonegawa; Xu Liu
Journal:  Front Behav Neurosci       Date:  2014-01-17       Impact factor: 3.558

Review 8.  From Engrams to Pathologies of the Brain.

Authors:  Christine A Denny; Evan Lebois; Steve Ramirez
Journal:  Front Neural Circuits       Date:  2017-04-07       Impact factor: 3.492

  8 in total

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