Evidence map›Paper›PMID 23973303›Full record

ArticleNeuroscience letters2013

Contribution of CA3 and CA1 pyramidal neurons to the tonic α7 nAChR-dependent glutamatergic input to CA1 pyramidal neurons.

Jyotirmoy Banerjee, Manickavasagom Alkondon, Edson X Albuquerque, Edna F R Pereira

Open access · greenAbstract read
In one paragraph

Article in Neuroscience letters, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

8 citing papers in PubMed, 12 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

4 authors at 1 institution in 1 country.

Jyotirmoy BanerjeeDivision of Translational Toxicology, Department of Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore, MD, United States. Electronic address: banerjee@umaryland.edu.
Manickavasagom Alkondon
Edson X Albuquerque
Edna F R Pereira
University of Maryland, Baltimore · US

Funding

Nicotinic receptors: Role in hippocampal synaptic functionR01NS025296 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI ALBUQUERQUE, EDSON X · 1987 to 2012
$3.9M
NINDS NIH HHS NS25296NINDS NIH HHS R01 NS025296
6 · The paper itself

Abstract

The Schaffer collaterals are among the major glutamatergic inputs to CA1 pyramidal neurons, the primary output of the hippocampus, which also receive sparse recurrent inputs from pyramidal neurons in the CA1 field. Although tonically active α7 nicotinic acetylcholine receptors (nAChRs) have been shown to sustain spontaneous glutamate transmission to CA1 pyramidal neurons in hippocampal slices under resting conditions, it remains to be determined whether these receptors are those expressed by CA3 or CA1 pyramidal neurons. This study was designed to test the hypothesis that the CA3 field of the hippocampus is a significant source of α7 nAChR-sustained glutamatergic transmission to CA1 pyramidal neurons. To this end, spontaneous excitatory postsynaptic currents (EPSCs) were recorded from CA1 and CA3 pyramidal neurons in intact rat hippocampal slices as well as from CA1 pyramidal neurons in CA3-ablated slices under various experimental conditions. Surgical removal of the CA3 region from the slices reduced by 20% the frequency of spontaneous EPSCs recorded from CA1 pyramidal neurons. This finding is in agreement with the concept that the CA3 field contributes significantly to the maintenance of spontaneous glutamatergic synaptic activity in CA1 pyramidal neurons. In addition, the α7 nAChR antagonist methyllycaconitine (MLA, 10nM) reduced the frequency of spontaneous EPSCs recorded from CA1 pyramidal neurons by 30% in intact slices and 12% in CA3-ablated slices. Taken together, these results demonstrate that tonically active α7 nAChRs in CA3 pyramidal neurons and/or in the Mossy fibers that innervate the CA3 pyramidal neurons do in fact contribute to the maintenance of glutamatergic synaptic activity in CA1 pyramidal neurons of hippocampal slices under resting conditions.

Indexed as

Aconitinealpha7 Nicotinic Acetylcholine ReceptorAnimalsCA1 Region, HippocampalCA3 Region, HippocampalExcitatory Postsynaptic PotentialsGlutamic AcidInhibitory Postsynaptic PotentialsIn Vitro TechniquesMalePyramidal CellsRats, Sprague-DawleySodium Channel BlockersSynaptic TransmissionTetrodotoxinAconitinealpha7 Nicotinic Acetylcholine ReceptorGlutamic AcidmethyllycaconitineSodium Channel BlockersTetrodotoxin2-amino-5-phosphonovaleric acid6-cyano-7-nitroquinoxaline-2,3-dioneACSFAPVartificial cerebrospinal fluidCNQXEPSCexcitatory postsynaptic currentHippocampusinhibitory postsynaptic currentIPSCmethyllycaconitineMethyllycaconitineMLAnAChRnicotinic acetylcholine receptorPyramidal neurontetrodotoxinTetrodotoxintime constant of decayTTXα7 nAChRτ(d)

Identifiers

PMID23973303
PMCPMC3825813
OpenAlexW2070662806

What OpenQuestion holds

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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.