Evidence map›Paper›PMID 31338915›Full record

ArticleThe European journal of neuroscience2019

Recruitment and disruption of ventral pallidal cue encoding during alcohol seeking.

David J Ottenheimer, Karen Wang, Alexandria Haimbaugh, Patricia H Janak, Jocelyn M Richard

Open access · greenAbstract read
In one paragraph

Article in The European journal of neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 18 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

5 authors at 2 institutions in 1 country.

David J OttenheimerSolomon H. Snyder Department of Neuroscience, Johns Hopkins School of Medicine, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0003-4882-1898
Karen WangDepartment of Psychological and Brain Sciences, Krieger School of Arts and Sciences, Johns Hopkins University, Baltimore, MD, USA.
Alexandria HaimbaughDepartment of Psychological and Brain Sciences, Krieger School of Arts and Sciences, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0001-9582-3226
Patricia H JanakSolomon H. Snyder Department of Neuroscience, Johns Hopkins School of Medicine, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0002-3333-9049
Jocelyn M RichardDepartment of Psychological and Brain Sciences, Krieger School of Arts and Sciences, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0001-5750-0418
Johns Hopkins University · USUniversity of Minnesota · US

Funding

Optogenetic Testing of Mechanims of Dopamine Action in Pavlovian LearningR01DA035943 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JANAK, PATRICIA H. · 2014 to 2023
$4.1M
Training Program in NeuroscienceT32NS091018 · NINDS · JOHNS HOPKINS UNIVERSITY · PI JAMES J KNIERIM, Daniel Hans O'Connor · 2015 to 2026
$4.1M
Context and Relapse to Ethanol-SeekingR01AA014925 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JANAK, PATRICIA H. · 2004 to 2014
$3.6M
Amygdala and Striatal Neural Circuits Controlling Alcohol IntakeR01AA026306 · NIAAA · JOHNS HOPKINS UNIVERSITY · PI JANAK, PATRICIA H. · 2018 to 2022
$1.8M
Ventral pallidal circuitry in alcohol seeking and reinstatement by stressR00AA025384 · NIAAA · UNIVERSITY OF MINNESOTA · PI RICHARD, JOCELYN M · 2018 to 2020
$747k
Accumbens shell mu-opioid signaling in alcohol self-administration and relapseF32AA022290 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RICHARD, JOCELYN M · 2013 to 2015
$153k
Ventral pallidal circuitry in alcohol seeking and reinstatement by stressK99AA025384 · NIAAA · JOHNS HOPKINS UNIVERSITY · PI RICHARD, JOCELYN M · 2017 to 2017
$139k
NIAAA NIH HHS F32 AA022290NIAAA NIH HHS K99 AA025384NIAAA NIH HHS R00 AA025384NIAAA NIH HHS R01 AA014925NIAAA NIH HHS R01 AA026306NIDA NIH HHS R01 DA035943NINDS NIH HHS T32 NS091018
6 · The paper itself

Abstract

A critical area of inquiry in the neurobiology of alcohol abuse is the mechanism by which cues gain the ability to elicit alcohol use. Previously, we found that cue-evoked activity in rat ventral pallidum robustly encodes the value of sucrose cues trained under both Pavlovian and instrumental contingencies, despite a stronger relationship between cue-evoked activity and behavioral latency after instrumental training (Richard et al., 2018, Elife, 7, e33107). Here, we assessed: (a) ventral pallidal representations of Pavlovian versus instrumental cues trained with alcohol reward, and (b) the impact of non-associative alcohol exposure on ventral pallidal representations of sucrose cues. Decoding of cue identity based on ventral pallidum firing was blunted for the Pavlovian alcohol cue in comparison to both the instrumental cue trained with alcohol and either cue type trained with sucrose. Further, non-associative alcohol exposure had opposing effects on ventral pallidal encoding of sucrose cues trained on instrumental versus Pavlovian associations, enhancing decoding accuracy for an instrumental discriminative stimulus and reducing decoding accuracy for a Pavlovian conditioned stimulus. These findings suggest that alcohol exposure can drive biased engagement of specific reward-related signals in the ventral pallidum.

Indexed as

Action PotentialsAnimalsBasal ForebrainConditioning, ClassicalConditioning, OperantCuesDrug-Seeking BehaviorEthanolFemaleMaleRatsSucroseEthanolSucrosealcohol exposureassociative learningdecodingelectrophysiologyreward

Identifiers

PMID31338915
PMCPMC6848750
OpenAlexW2963441358

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.