Evidence map›Paper›PMID 29981255›Full record

ArticleHippocampus2020

Age-associated changes in waking hippocampal sharp-wave ripples.

Stephen L Cowen, Daniel T Gray, Jean-Paul L Wiegand, Lesley A Schimanski, Carol A Barnes

Abstract read
In one paragraph

Article in Hippocampus, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Article
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Interictal epileptiform discharges affect memory in an Alzheimer's disease mouse model.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Spectrum Degradation of Hippocampal LFP During Euthanasia.Frontiers in systems neuroscience · 2021
    Article
  15. Review
  16. Article
  17. Article
  18. A Role for Matrix Metalloproteases in Antidepressant Efficacy.Frontiers in molecular neuroscience · 2019
    Review
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Stephen L CowenEvelyn F. McKnight Brain Institute, University of Arizona, Tucson, Arizona, 85724.
Daniel T GrayEvelyn F. McKnight Brain Institute, University of Arizona, Tucson, Arizona, 85724.
Jean-Paul L WiegandEvelyn F. McKnight Brain Institute, University of Arizona, Tucson, Arizona, 85724.
Lesley A SchimanskiEvelyn F. McKnight Brain Institute, University of Arizona, Tucson, Arizona, 85724.
Carol A BarnesEvelyn F. McKnight Brain Institute, University of Arizona, Tucson, Arizona, 85724.

Funding

NEUROBEHAVIORAL RELATIONS IN SENESCENT HIPPOCAMPUSR01AG003376 · NIA · UNIVERSITY OF COLORADO AT BOULDER · PI BARNES, CAROL A. · 1985 to 2025
$16.4M
Cell Assemblies, Pattern Completion and the Aging BrainR37AG012609 · NIA · UNIVERSITY OF ARIZONA · PI BARNES, CAROL A. · 2004 to 2013
$3.0M
CELL ASSEMBLIES, PATTERN COMPLETION, AND THE AGING BRAINR01AG012609 · NIA · UNIVERSITY OF ARIZONA · PI BARNES, CAROL A. · 1994 to 2003
$1.2M
Neurobiological basis of age-related deficits in attentional shifting and monitoringF31AG055263 · NIA · UNIVERSITY OF ARIZONA · PI GRAY, DANIEL · 2016 to 2018
$71k
NIA NIH HHS F31 AG055263NIA NIH HHS R01 AG003376NIA NIH HHS R01 AG012609NIA NIH HHS R37 AG012609
6 · The paper itself

Abstract

Hippocampal sharp-wave ripples are brief high-frequency (120-250 Hz) oscillatory events that support mnemonic processes during sleep and awake behavior. Although ripples occurring during sleep are believed to facilitate memory consolidation, waking ripples may also be involved in planning and memory retrieval. Recent work from our group determined that normal aging results in a significant reduction in the peak oscillatory frequency and rate-of-occurrence of ripples during sleep that may contribute to age-associated memory decline. It is unknown, however, how aging alters waking ripples. We investigated whether characteristics of waking ripples undergo age-dependent changes. Sharp-wave ripple events were recorded from the CA1 region of the hippocampus in old (n = 5) and young (n = 6) F344 male rats as they performed a place-dependent eyeblink conditioning task. Several novel observations emerged from this analysis. First, although aged rats expressed more waking ripples than young rats during track running and reward consumption, this effect was eliminated, and, in the case of track-running, reversed when time spent in each location was accounted for. Thus, aged rats emit more ripples, but young rats express a higher ripple rate. This likely results from reduced locomotor activity in aged animals. Furthermore, although ripple rates increased as young rats approached rewards, rates did not increase in aged rats, and rates in aged and young animals were not affected by eyeblink conditioning. Finally, although the oscillatory frequency of ripples was lower in aged animals during rest, frequencies in aged rats increased during behavior to levels indistinguishable from young rats. Given the involvement of waking ripples in memory retrieval, a possible consequence of slower movement speeds of aged animals is to provide more opportunity to replay task-relevant information and compensate for age-related declines in ripple rate during task performance.

Indexed as

Age FactorsAgingAnimalsBrain WavesConditioning, EyelidHippocampusMaleMemoryMotor ActivityRatsRats, Inbred F344Wakefulnessoscillationreactivationworking memory

Identifiers

PMID29981255
PMCPMC6322975

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.