Evidence map›Paper›PMID 34531380›Full record

ArticleNature communications2021

Acetylcholine prioritises direct synaptic inputs from entorhinal cortex to CA1 by differential modulation of feedforward inhibitory circuits.

Jon Palacios-Filardo, Matt Udakis, Giles A Brown, Benjamin G Tehan, Miles S Congreve, Pradeep J Nathan, Alastair J H Brown, Jack R Mellor

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.2field-weighted citation impact, top 7% 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, 43 citations in OpenAlex.

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  17. Differential Regulation of Prelimbic and Thalamic Transmission to the Basolateral Amygdala by Acetylcholine Receptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Jon Palacios-FilardoCenter for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience, University of Bristol, University Walk, Bristol, UK.
Matt UdakisCenter for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience, University of Bristol, University Walk, Bristol, UK.
Giles A BrownSosei Heptares, Steinmetz Building, Granta Park, Great Abingdon, Cambridge, UK.
Benjamin G TehanSosei Heptares, Steinmetz Building, Granta Park, Great Abingdon, Cambridge, UK.
Miles S CongreveSosei Heptares, Steinmetz Building, Granta Park, Great Abingdon, Cambridge, UK.
Pradeep J NathanDepartment of Psychiatry, University of Cambridge, Cambridge, UK.
Alastair J H BrownSosei Heptares, Steinmetz Building, Granta Park, Great Abingdon, Cambridge, UK.
Jack R MellorCenter for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience, University of Bristol, University Walk, Bristol, UK. Jack.Mellor@Bristol.ac.uk.ORCID http://orcid.org/0000-0002-7706-8105
Heptares Therapeutics (United Kingdom) · GBUniversity of Bristol · GBUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research CouncilWellcome TrustWellcome Trust 101029
6 · The paper itself

Abstract

Acetylcholine release in the hippocampus plays a central role in the formation of new memory representations. An influential but largely untested theory proposes that memory formation requires acetylcholine to enhance responses in CA1 to new sensory information from entorhinal cortex whilst depressing inputs from previously encoded representations in CA3. Here, we show that excitatory inputs from entorhinal cortex and CA3 are depressed equally by synaptic release of acetylcholine in CA1. However, feedforward inhibition from entorhinal cortex exhibits greater depression than CA3 resulting in a selective enhancement of excitatory-inhibitory balance and CA1 activation by entorhinal inputs. Entorhinal and CA3 pathways engage different feedforward interneuron subpopulations and cholinergic modulation of presynaptic function is mediated differentially by muscarinic M

Indexed as

AcetylcholineAnimalsCA1 Region, HippocampalCarbacholCholinergic AgonistsEntorhinal CortexExcitatory Postsynaptic PotentialsFeedback, PhysiologicalInterneuronsMaleMiceMice, Inbred C57BLMice, KnockoutPatch-Clamp TechniquesPyramidal CellsReceptor, Muscarinic M3AcetylcholineCarbacholCholinergic AgonistsReceptor, Muscarinic M3

Identifiers

PMID34531380
PMCPMC8445995
OpenAlexW3200062240

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.