Evidence map›Paper›PMID 30242046›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2018

Convergent Metabotropic Signaling Pathways Inhibit SK Channels to Promote Synaptic Plasticity in the Hippocampus.

Cezar M Tigaret, Sophie E L Chamberlain, Joseph H L P Sadowski, Jeremy Hall, Michael C Ashby, Jack R Mellor

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. The small conductance CaNeuropharmacology · 2024
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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

6 authors at 2 institutions in 1 country.

Cezar M TigaretCentre for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, BS8 1TD, United Kingdom and.ORCID 0000-0001-5848-6697
Sophie E L ChamberlainCentre for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, BS8 1TD, United Kingdom and.
Joseph H L P SadowskiCentre for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, BS8 1TD, United Kingdom and.
Jeremy HallNeuroscience and Mental Health Research Institute, School of Medicine, Cardiff University, Cardiff, CF24 4HQ, United Kingdom.
Michael C AshbyCentre for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, BS8 1TD, United Kingdom and.ORCID 0000-0002-8593-8473
Jack R MellorCentre for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol, BS8 1TD, United Kingdom and Jack.Mellor@Bristol.ac.uk.ORCID 0000-0002-7706-8105
University of Bristol · GBCardiff University · GB

Funding

Medical Research Council MR/J013188/1Medical Research Council MR/L010305/1Medical Research Council MR/R011397/1Wellcome Trust
6 · The paper itself

Abstract

Hebbian synaptic plasticity at hippocampal Schaffer collateral synapses is tightly regulated by postsynaptic small conductance (SK) channels that restrict NMDA receptor activity. SK channels are themselves modulated by G-protein-coupled signaling pathways, but it is not clear under what conditions these are activated to enable synaptic plasticity. Here, we show that muscarinic M1 receptor (M1R) and type 1 metabotropic glutamate receptor (mGluR1) signaling pathways, which are known to inhibit SK channels and thereby disinhibit NMDA receptors, converge to facilitate spine calcium transients during the induction of long-term potentiation (LTP) at hippocampal Schaffer collateral synapses onto CA1 pyramidal neurons of male rats. Furthermore, mGluR1 activation is required for LTP induced by reactivated place-cell firing patterns that occur in sharp-wave ripple events during rest or sleep. In contrast, M1R activation is required for LTP induced by place-cell firing patterns during exploration. Thus, we describe a common mechanism that enables synaptic plasticity during both encoding and consolidation of memories within hippocampal circuits.

Indexed as

AnimalsApaminExcitatory Amino Acid AgonistsExcitatory Postsynaptic PotentialsHippocampusMaleMicroscopy, Fluorescence, MultiphotonNeuronal PlasticityOrgan Culture TechniquesRatsRats, WistarReceptor, Muscarinic M1Signal TransductionSmall-Conductance Calcium-Activated Potassium ChannelsApaminExcitatory Amino Acid AgonistsReceptor, Muscarinic M1Small-Conductance Calcium-Activated Potassium Channelshippocampusmetabotropic glutamate receptorsmuscarinic receptorsSK channelsspike timing-dependent plasticitysynaptic plasticity

Identifiers

PMID30242046
PMCPMC6199408
OpenAlexW2891518121

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.