Evidence map›Paper›PMID 38258622›Full record

ArticleThe European journal of neuroscience2024

Cholinergic modulation of rearing in rats performing a spatial memory task.

Skylar Cassity, Irene Jungyeon Choi, Billy Howard Gregory, Adeleke Malik Igbasanmi, Sarah Cristi Bickford, Kiara Tyanni Moore, Anna Elisabeth Seraiah, Dylan Layfield, Ehren Lee Newman

Open access · hybridAbstract read
In one paragraph

Article in The European journal of neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 4 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Skylar CassityDepartment of Psychological and Brain Sciences, College of Arts and Sciences, Indiana University Bloomington, Bloomington, Indiana, USA.
Irene Jungyeon ChoiDepartment of Psychological and Brain Sciences, College of Arts and Sciences, Indiana University Bloomington, Bloomington, Indiana, USA.
Billy Howard GregoryDepartment of Psychological and Brain Sciences, College of Arts and Sciences, Indiana University Bloomington, Bloomington, Indiana, USA.
Adeleke Malik IgbasanmiDepartment of Psychological and Brain Sciences, College of Arts and Sciences, Indiana University Bloomington, Bloomington, Indiana, USA.
Sarah Cristi BickfordDepartment of Psychological and Brain Sciences, College of Arts and Sciences, Indiana University Bloomington, Bloomington, Indiana, USA.
Kiara Tyanni MooreDepartment of Psychological and Brain Sciences, College of Arts and Sciences, Indiana University Bloomington, Bloomington, Indiana, USA.
Anna Elisabeth SeraiahPrinceton Neuroscience Institute, Princeton University, Princeton, New Jersey, USA.
Dylan LayfieldDepartment of Psychological and Brain Sciences, College of Arts and Sciences, Indiana University Bloomington, Bloomington, Indiana, USA.
Ehren Lee NewmanDepartment of Psychological and Brain Sciences, College of Arts and Sciences, Indiana University Bloomington, Bloomington, Indiana, USA.ORCID 0000-0001-7006-4112
Indiana University Bloomington · USEngineering Systems (United States) · USPrinceton University · US

Funding

CRCNS: Scale-invariant navigation and its degradation in Alzheimer's diseaseR01AG076198 · NIA · TRUSTEES OF INDIANA UNIVERSITY · PI NEWMAN, EHREN L. · 2021 to 2023
$1.0M
NIA NIH HHS R01 AG076198
6 · The paper itself

Abstract

Spatial memory encoding depends in part on cholinergic modulation. How acetylcholine supports spatial memory encoding is not well understood. Prior studies indicate that acetylcholine release is correlated with exploration, including epochs of rearing onto hind legs. Here, to test whether elevated cholinergic tone increases the probability of rearing, we tracked rearing frequency and duration while optogenetically modulating the activity of choline acetyltransferase containing (i.e., acetylcholine producing) neurons of the medial septum in rats performing a spatial working memory task (n = 17 rats). The cholinergic neurons were optogenetically inhibited using halorhodopsin for the duration that rats occupied two of the four open arms during the study phase of an 8-arm radial arm maze win-shift task. Comparing rats' behaviour in the two arm types showed that rearing frequency was not changed, but the average duration of rearing epochs became significantly longer. This effect on rearing was observed during optogenetic inhibition but not during sham inhibition or in rats that received infusions of a fluorescent reporter virus (i.e., without halorhodopsin; n = 6 rats). Optogenetic inhibition of cholinergic neurons during the pretrial waiting phase had no significant effect on rearing, indicating a context-specificity of the observed effects. These results are significant in that they indicate that cholinergic neuron activity in the medial septum is correlated with rearing not because it motivates an exploratory state but because it contributes to the processing of information acquired while rearing.

Indexed as

Cholinergic NeuronsOptogeneticsSpatial MemoryAcetylcholineAnimalsCholine O-AcetyltransferaseMaleMaze LearningMemory, Short-TermRatsRats, Long-EvansAcetylcholineCholine O-Acetyltransferaseacetylcholineexplorationhippocampusmedial septumoptogeneticsratrearingreversible inactivationspatial memory

Identifiers

PMID38258622
PMCPMC11076174
OpenAlexW4391140253

What OpenQuestion holds

Textmetadata
LicenceTDM
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.