Evidence map›Paper›PMID 27093059›Full record

ArticlePLoS computational biology2016

Hippocampal CA1 Ripples as Inhibitory Transients.

Paola Malerba, Giri P Krishnan, Jean-Marc Fellous, Maxim Bazhenov

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
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

28 citing papers in PubMed, 59 citations in OpenAlex.

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  12. Neuregulin 1 and ErbB4 Kinase Actively Regulate Sharp Wave Ripples in the Hippocampus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  13. Sequential Attractors in Combinatorial Threshold-Linear Networks.SIAM journal on applied dynamical systems · 2022
    Article
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  18. Mechanisms of neural organization and rhythmogenesis during hippocampal and cortical ripples.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
  19. Article
  20. Large time step discrete-time modeling of sharp wave activity in hippocampal area CA3.Communications in nonlinear science & numerical simulation · 2019
    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

4 authors at 2 institutions in 1 country.

Paola MalerbaDepartment of Cell Biology and Neuroscience, University of California Riverside, Riverside, California, United States of America.ORCID http://orcid.org/0000-0002-8733-899X
Giri P KrishnanDepartment of Cell Biology and Neuroscience, University of California Riverside, Riverside, California, United States of America.
Jean-Marc FellousDepartment of Psychology, University of Arizona, Tucson, Arizona, United States of America.
Maxim BazhenovDepartment of Cell Biology and Neuroscience, University of California Riverside, Riverside, California, United States of America.
University of California, Riverside · USUniversity of Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Memories are stored and consolidated as a result of a dialogue between the hippocampus and cortex during sleep. Neurons active during behavior reactivate in both structures during sleep, in conjunction with characteristic brain oscillations that may form the neural substrate of memory consolidation. In the hippocampus, replay occurs within sharp wave-ripples: short bouts of high-frequency activity in area CA1 caused by excitatory activation from area CA3. In this work, we develop a computational model of ripple generation, motivated by in vivo rat data showing that ripples have a broad frequency distribution, exponential inter-arrival times and yet highly non-variable durations. Our study predicts that ripples are not persistent oscillations but result from a transient network behavior, induced by input from CA3, in which the high frequency synchronous firing of perisomatic interneurons does not depend on the time scale of synaptic inhibition. We found that noise-induced loss of synchrony among CA1 interneurons dynamically constrains individual ripple duration. Our study proposes a novel mechanism of hippocampal ripple generation consistent with a broad range of experimental data, and highlights the role of noise in regulating the duration of input-driven oscillatory spiking in an inhibitory network.

Indexed as

Models, NeurologicalAnimalsCA1 Region, HippocampalCA3 Region, HippocampalCerebral CortexComputational BiologyHumansInterneuronsMemory ConsolidationModels, AnimalModels, PsychologicalNerve NetPyramidal CellsRatsRats, Inbred BNSleep

Identifiers

PMID27093059
PMCPMC4836732
OpenAlexW2339730246

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.