Evidence map›Paper›PMID 32710688›Full record

ArticleHippocampus2020

Optogenetic "low-theta" pacing of the septohippocampal circuit is sufficient for spatial goal finding and is influenced by behavioral state and cognitive demand.

Philippe R Mouchati, Michelle L Kloc, Gregory L Holmes, Sheryl L White, Jeremy M Barry

Open access · greenAbstract 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 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 31 citations in OpenAlex.

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  13. Site-dependent shaping of field potential waveforms.Cerebral cortex (New York, N.Y. : 1991) · 2023
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  17. PTEN Regulates Dendritic Arborization by Decreasing Microtubule Polymerization Rate.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
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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 at 1 institution in 1 country.

Philippe R MouchatiEpilepsy Cognition and Development Group, Department of Neurological Sciences, Larner College of Medicine, University of Vermont, Burlington, Vermont, USA.
Michelle L KlocEpilepsy Cognition and Development Group, Department of Neurological Sciences, Larner College of Medicine, University of Vermont, Burlington, Vermont, USA.
Gregory L HolmesEpilepsy Cognition and Development Group, Department of Neurological Sciences, Larner College of Medicine, University of Vermont, Burlington, Vermont, USA.
Sheryl L WhiteEpilepsy Cognition and Development Group, Department of Neurological Sciences, Larner College of Medicine, University of Vermont, Burlington, Vermont, USA.
Jeremy M BarryEpilepsy Cognition and Development Group, Department of Neurological Sciences, Larner College of Medicine, University of Vermont, Burlington, Vermont, USA.ORCID 0000-0002-7843-332X
University of Vermont · US

Funding

Cognitive Deficits After Experimental Febrile Seizures: Neurobiology & BiomarkersR01NS108296 · NINDS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI BARAM, TALLIE Z., HOLMES, GREGORY L. · 2018 to 2022
$2.6M
Mechanisms of Cognitive Impairment Following Early-Life SeizuresR01NS108765 · NINDS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI HOLMES, GREGORY L. · 2018 to 2022
$1.9M
NINDS NIH HHS R01 NS108296NINDS NIH HHS R01 NS108765
6 · The paper itself

Abstract

Hippocampal theta oscillations show prominent changes in frequency and amplitude depending on behavioral state or cognitive demands. How these dynamic changes in theta oscillations contribute to the spatial and temporal organization of hippocampal cells, and ultimately behavior, remain unclear. We used low-theta frequency optogenetic stimulation to pace coordination of cellular and network activity between the medial septum (MS) and hippocampus during baseline and MS stimulation while rats were at rest or performing a spatial accuracy task with a visible or hidden goal zone. Hippocampal receptivity to pan-neuronal septal stimulation at low-theta frequency was primarily determined by speed and secondarily by task demands. Competition between artificial and endogenous field potentials at theta frequency attenuated hippocampal phase preference relative to local theta, but the spike-timing activity of hippocampal pyramidal cells was effectively driven by artificial septal output, particularly during the hidden goal task. Notwithstanding temporal reorganization by artificial theta stimulation, place field properties were unchanged and alterations to spatial behavior were limited to goal zone approximation. Our results indicate that even a low-theta frequency timing signal in the septohippocampal circuit is sufficient for spatial goal finding behavior. The results also advance a mechanistic understanding of how endogenous or artificial somatodendritic timing signals relate to displacement computations during navigation and spatial memory.

Indexed as

GoalsAnimalsCognitionElectric StimulationElectrodes, ImplantedHippocampusMaleNerve NetOptogeneticsRatsRats, Sprague-DawleySeptum of BrainSpatial MemoryTheta Rhythmartificial theta stimulationhippocampusmemoryspatial behaviortheta

Identifiers

PMID32710688
PMCPMC7902092
OpenAlexW3043857630

What OpenQuestion holds

Textmetadata
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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.