Evidence map›Paper›PMID 35489331›Full record

ArticleNeuron2022

Ripple-selective GABAergic projection cells in the hippocampus.

Gergely G Szabo, Jordan S Farrell, Barna Dudok, Wen-Hsien Hou, Anna L Ortiz, Csaba Varga, Prannath Moolchand, Cafer Ikbal Gulsever, Tilo Gschwind, Jordane Dimidschstein and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Neuron, 2022. 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
6.4field-weighted citation impact, top 2% 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, 63 citations in OpenAlex.

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  15. Distinct Functional Classes of CA1 Hippocampal Interneurons Are Modulated by Cerebellar Stimulation in a Coordinated Manner.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  16. Article
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  18. Aberrant hippocampal CabioRxiv : the preprint server for biology · 2024
    Article
  19. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Gergely G SzaboDepartment of Neurosurgery, Stanford University, Stanford, CA, USA. Electronic address: szergely@stanford.edu.
Jordan S FarrellDepartment of Neurosurgery, Stanford University, Stanford, CA, USA.
Barna DudokDepartment of Neurosurgery, Stanford University, Stanford, CA, USA.
Wen-Hsien HouDepartment of Biomedicine, Aarhus University, Aarhus, Denmark; DANDRITE, The Danish Research Institute of Translational Neuroscience, Aarhus University, Aarhus, Denmark.
Anna L OrtizDepartment of Neurosurgery, Stanford University, Stanford, CA, USA.
Csaba VargaDepartment of Neurosurgery, Stanford University, Stanford, CA, USA.
Prannath MoolchandDepartment of Neurosurgery, Stanford University, Stanford, CA, USA.
Cafer Ikbal GulseverDepartment of Neurosurgery, Stanford University, Stanford, CA, USA.
Tilo GschwindDepartment of Neurosurgery, Stanford University, Stanford, CA, USA.
Jordane DimidschsteinStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Marco CapognaDepartment of Biomedicine, Aarhus University, Aarhus, Denmark; DANDRITE, The Danish Research Institute of Translational Neuroscience, Aarhus University, Aarhus, Denmark; Center for Proteins in Memory - PROMEMO, Danish National Research Foundation, Aarhus University, Aarhus, Denmark.
Ivan SolteszDepartment of Neurosurgery, Stanford University, Stanford, CA, USA.
Stanford University · USAarhus University · DKBroad Institute · USStanford Medicine · US

Funding

Towards a Complete Description of the Circuitry Underlying Sharp Wave-Mediated Memory ReplayU19NS104590 · NINDS · STANFORD UNIVERSITY · PI SOLTESZ, IVAN · 2017 to 2021
$13.2M
Cannabinoid control of epilepsyR01NS099457 · NINDS · STANFORD UNIVERSITY · PI SOLTESZ, IVAN · 2017 to 2021
$1.8M
Perisomatic inhibition in epilepsyK99NS117795 · NINDS · STANFORD UNIVERSITY · PI DUDOK, BARNA · 2020 to 2021
$177k
NINDS NIH HHS K99 NS117795NINDS NIH HHS R01 NS099457NINDS NIH HHS U19 NS104590
6 · The paper itself

Abstract

Ripples are brief high-frequency electrographic events with important roles in episodic memory. However, the in vivo circuit mechanisms coordinating ripple-related activity among local and distant neuronal ensembles are not well understood. Here, we define key characteristics of a long-distance projecting GABAergic cell group in the mouse hippocampus that selectively exhibits high-frequency firing during ripples while staying largely silent during theta-associated states when most other GABAergic cells are active. The high ripple-associated firing commenced before ripple onset and reached its maximum before ripple peak, with the signature theta-OFF, ripple-ON firing pattern being preserved across awake and sleep states. Controlled by septal GABAergic, cholinergic, and CA3 glutamatergic inputs, these ripple-selective cells innervate parvalbumin and cholecystokinin-expressing local interneurons while also targeting a variety of extra-hippocampal regions. These results demonstrate the existence of a hippocampal GABAergic circuit element that is uniquely positioned to coordinate ripple-related neuronal dynamics across neuronal assemblies.

Indexed as

HippocampusInterneuronsAnimalsMiceNeuronsParvalbuminsWakefulnessParvalbuminsbrain statedisinhibitionGABAhippocampusinhibitionmedial septummuscarinicsharp-wave ripplesleep

Identifiers

PMID35489331
PMCPMC9233074
OpenAlexW4225120299

What OpenQuestion holds

Textmetadata
LicenceTDM
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.