Evidence map›Paper›PMID 30926750›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2019

GABAergic Medial Septal Neurons with Low-Rhythmic Firing Innervating the Dentate Gyrus and Hippocampal Area CA3.

Minas Salib, Abhilasha Joshi, Linda Katona, Michael Howarth, Benjamin R Micklem, Peter Somogyi, Tim J Viney

Open access · hybridAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.7field-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

31 citing papers in PubMed, 52 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Minas SalibDepartment of Pharmacology, University of Oxford, Oxford OX1 3QT, United Kingdom tim.viney@pharm.ox.ac.uk minas.salib@pharm.ox.ac.uk.ORCID 0000-0001-9938-7978
Abhilasha JoshiDepartment of Pharmacology, University of Oxford, Oxford OX1 3QT, United Kingdom.ORCID 0000-0002-0511-3747
Linda KatonaDepartment of Pharmacology, University of Oxford, Oxford OX1 3QT, United Kingdom.ORCID 0000-0002-9942-4502
Michael HowarthDepartment of Pharmacology, University of Oxford, Oxford OX1 3QT, United Kingdom.
Benjamin R MicklemDepartment of Pharmacology, University of Oxford, Oxford OX1 3QT, United Kingdom.ORCID 0000-0002-0315-6022
Peter SomogyiDepartment of Pharmacology, University of Oxford, Oxford OX1 3QT, United Kingdom.ORCID 0000-0001-7650-684X
Tim J VineyDepartment of Pharmacology, University of Oxford, Oxford OX1 3QT, United Kingdom tim.viney@pharm.ox.ac.uk minas.salib@pharm.ox.ac.uk.ORCID 0000-0001-6444-1188
University of Oxford · GB

Funding

Medical Research Council MC_ST_U15010Medical Research Council MC_UU_12024/4Medical Research Council MR/R011567/1Wellcome TrustWellcome Trust 108726/Z/15/Z
6 · The paper itself

Abstract

The medial septum implements cortical theta oscillations, a 5-12 Hz rhythm associated with locomotion and paradoxical sleep reflecting synchronization of neuronal assemblies such as place cell sequence coding. Highly rhythmic burst-firing parvalbumin-positive GABAergic medial septal neurons are strongly coupled to theta oscillations and target cortical GABAergic interneurons, contributing to coordination within one or several cortical regions. However, a large population of medial septal neurons of unidentified neurotransmitter phenotype and with unknown axonal target areas fire with a low degree of rhythmicity. We investigated whether low-rhythmic-firing neurons (LRNs) innervated similar or different cortical regions to high-rhythmic-firing neurons (HRNs) and assessed their temporal dynamics in awake male mice. The majority of LRNs were GABAergic and parvalbumin-immunonegative, some expressing calbindin; they innervated interneurons mostly in the dentate gyrus (DG) and CA3. Individual LRNs showed several distinct firing patterns during immobility and locomotion, forming a parallel inhibitory stream for the modulation of cortical interneurons. Despite their fluctuating firing rates, the preferred firing phase of LRNs during theta oscillations matched the highest firing probability phase of principal cells in the DG and CA3. In addition, as a population, LRNs were markedly suppressed during hippocampal sharp-wave ripples, had a low burst incidence, and several of them did not fire on all theta cycles. Therefore, CA3 receives GABAergic input from both HRNs and LRNs, but the DG receives mainly LRN input. We propose that distinct GABAergic LRNs contribute to changing the excitability of the DG and CA3 during memory discrimination via transient disinhibition of principal cells.

Indexed as

Action PotentialsAnimalsCA3 Region, HippocampalCalbindinsDentate GyrusGABAergic NeuronsMaleMemory, EpisodicMental RecallMiceMice, Inbred C57BLNerve Tissue ProteinsNeural PathwaysParvalbuminsRunningSeptum of BrainCalbindinsNerve Tissue ProteinsParvalbuminsdentate gyrushippocampusinhibitionmedial septumoscillationsrhythmicity

Identifiers

PMID30926750
PMCPMC6554630
OpenAlexW2930145255

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.