Evidence map›Paper›PMID 24453319›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Firing of hippocampal neurogliaform cells induces suppression of synaptic inhibition.

Gengyu Li, Robert Stewart, Marco Canepari, Marco Capogna

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  4. Review
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  8. Article
  9. Neurogliaform cells in cortical circuits.Nature reviews. Neuroscience · 2015
    Review
  10. Article
  11. Article
  12. 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 2 countries.

Gengyu LiMedical Research Council Anatomical Neuropharmacology Unit, Department of Pharmacology, University of Oxford, Oxford 0X1 3TH, United Kingdom; Inserm U836, Team 3, Grenoble Cedex 09, France, Université Joseph Fourier, Grenoble Institut des Neurosciences and Laboratoire Interdisciplinare de Physique, CNRS UMR 5588, Grenoble Cedex 09, France, and Laboratories of Excellence, Ion Channel Science and Therapeutics, Inserm U836, Grenoble Cedex 09, France.
Robert Stewart
Marco Canepari
Marco Capogna
Centre National de la Recherche Scientifique · FRUniversity of Oxford · GB

Funding

Medical Research Council MC_U138197106Medical Research Council MC_UU_12020/2Medical Research Council U138197106
6 · The paper itself

Abstract

Little is known about how neuron firing recorded in vivo retrogradely influences synaptic strength. We injected the firing of a rat hippocampal neurogliaform cell (NGFC), a widely expressed GABAergic neuron type, detected in vivo during theta rhythm, into NGFCs of rat or neuronal nitric oxide synthase (nNOS)-Cre-tdTomato mouse recorded in vitro. We found that the "in vivo firing pattern" produced a transient firing-induced suppression of synaptic inhibition (FSI) evoked by a presynaptic NGFC. Imaging experiments demonstrate that FSI was associated with action potential backpropagation (bAP) and a supralinear increase in dendritic Ca(2+). The application of the L-type Ca(2+) channel antagonist nimodipine blocked FSI. Further pharmacological experiments, such as the application of a nitric oxide-sensitive guanylyl cyclase (NO-sGC) receptor antagonist, a NOS inhibitor, and NO donors, suggested that NO released from postsynaptic cells mediated FSI and likely activated presynaptic receptors to inhibit GABA release. The in vivo firing pattern modulated the size of unitary EPSPs impinging on NGFCs through FSI and not via a direct effect on excitatory synaptic transmission. Our data demonstrate: (1) retrograde signaling initiated by in vivo firing pattern, (2) interneuron bAPs detected with fast temporal resolution, and (3) a novel role for NO expressed by specific interneuron types.

Indexed as

AnimalsExcitatory Postsynaptic PotentialsFemaleHippocampusInterneuronsMaleMice, TransgenicNeural InhibitionNeuronal PlasticityNeurotransmitter AgentsNitric OxidePatch-Clamp TechniquesRatsSynapsesSynaptic TransmissionNeurotransmitter AgentsNitric Oxidehippocampusimaginginterneuronnitric oxideretrograde messengerssynaptic transmission

Identifiers

PMID24453319
PMCPMC3898288
OpenAlexW2031729231

What OpenQuestion holds

Textmetadata
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.