Evidence map›Paper›PMID 26828299›Full record

ArticleNeuroscience letters2016

Ventral tegmental area muscarinic receptors modulate depression and anxiety-related behaviors in rats.

Keri M Small, Eric Nunes, Shannon Hughley, Nii A Addy

Open access · greenAbstract read
In one paragraph

Article in Neuroscience letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
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  7. Potential of Heterogeneous Compounds as Antidepressants: A Narrative Review.International journal of molecular sciences · 2022
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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.

Keri M SmallDepartment of Psychiatry, Yale School of Medicine, New Haven, CT 06511, United States.
Eric NunesDepartment of Psychiatry, Yale School of Medicine, New Haven, CT 06511, United States.
Shannon HughleyDepartment of Psychiatry, Yale School of Medicine, New Haven, CT 06511, United States.
Nii A AddyDepartment of Psychiatry, Yale School of Medicine, New Haven, CT 06511, United States; Department of Cellular and Molecular Physiology, New Haven, CT 06511, United States; Interdepartmental Neuroscience Program, Yale University, New Haven, CT 06511, United States. Electronic address: nii.addy@yale.edu.
Yale University · US

Funding

RESEARCH TRAINING - BIOLOGICAL SCIENCEST32MH014276 · NIMH · YALE UNIVERSITY · PI Marina R Picciotto · 1985 to 2026
$7.2M
Role of mTOR and Synaptogenesis in the Actions of Rapid-Acting AntidepressantsR01MH093897 · NIMH · YALE UNIVERSITY · PI DILEONE, RALPH J · 2011 to 2021
$5.0M
Yale Postbaccalaureate Research Education ProgramR25GM104553 · NIGMS · YALE UNIVERSITY · PI BENNETT, ANTON M, NEARON, MICHELLE · 2014 to 2017
$1.3M
CaV 1.3 L-type Calcium Channel Mechanisms in Cocaine SeekingR21DA038048 · NIDA · YALE UNIVERSITY · PI ADDY, NII A · 2014 to 2015
$472k
NIDA NIH HHS R21 DA038048NIGMS NIH HHS R25 GM104553NIMH NIH HHS R01 MH093897NIMH NIH HHS T32 MH014276
6 · The paper itself

Abstract

Cholinergic and dopaminergic mechanisms within the mesolimbic dopamine system are suggested to play a role in the manifestation of depression and anxiety-related disorders. However, despite the fact that cholinergic mechanisms in the ventral tegmental area (VTA) highly regulate dopamine activity, the role of VTA cholinergic mechanisms in depression-related behaviors is relatively unknown. Here we sought to determine whether enhancing cholinergic tone in the VTA would alter depression and anxiety-related behavior in the forced swim test (FST), elevated plus maze (EPM) and sucrose preference test (SPT). Adult Sprague Dawley male rats received VTA infusion of the acetylcholinesterase inhibitor, physostigmine (0, 1, 2μg/side), immediately prior to the FST, EPM, or SPT. Physostigmine administration increased immobility time in the FST, decreased time spent on open arms in the EPM, and decreased sucrose preference. We also examined whether activation of VTA muscarinic receptors was sufficient to alter behavior in the FST and EPM. Similar to physostigmine, VTA infusion of the muscarinic receptor agonist, pilocarpine (0, 3, 30μg/side), increased immobility time in the FST and decreased time spent on open arms in the EPM. These data suggest that enhanced VTA cholinergic tone promotes pro-depressive and anxiogenic-like effects and demonstrate that specific activation of VTA muscarinic receptors is also sufficient to induce pro-depressive and anxiogenic responses. Together, these findings reveal a novel role of VTA cholinergic, and specifically muscarinic receptor, mechanisms in mediating responses to stress and anxiety.

Indexed as

Behavior, AnimalAnimalsAnxietyCholinesterase InhibitorsDepressionFood PreferencesMaleMaze LearningMotor ActivityMuscarinic AgonistsPhysostigminePilocarpineRats, Sprague-DawleyReceptors, MuscarinicVentral Tegmental AreaCholinesterase InhibitorsMuscarinic AgonistsPhysostigminePilocarpineReceptors, MuscarinicAcetylcholineAnxietyDepressionMesolimbic dopamine systemMuscarinic receptorVentral tegmental area

Identifiers

PMID26828299
PMCPMC4798862
OpenAlexW2257827475

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.