Evidence map›Paper›PMID 32556583›Full record

ArticleBrain structure & function2020

Reward-related dynamical coupling between basolateral amygdala and nucleus accumbens.

Chia-Chun Hsu, Teresa E Madsen, Elizabeth O'Gorman, Shannon L Gourley, Donald G Rainnie

Open access · greenAbstract read
In one paragraph

Article in Brain structure & function, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  5. CaNature communications · 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

5 authors at 2 institutions in 1 country.

Chia-Chun HsuYerkes National Primate Research Center, Emory University, Atlanta, USA.ORCID http://orcid.org/0000-0002-5930-0484
Teresa E MadsenYerkes National Primate Research Center, Emory University, Atlanta, USA.
Elizabeth O'GormanYerkes National Primate Research Center, Emory University, Atlanta, USA.
Shannon L GourleyYerkes National Primate Research Center, Emory University, Atlanta, USA. shannon.l.gourley@emory.edu.ORCID http://orcid.org/0000-0002-7783-9379
Donald G RainnieYerkes National Primate Research Center, Emory University, Atlanta, USA. tigrainnie@gmail.com.
Emory University · USEmory Healthcare · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
The Impact of Oxytocin on the Neural Representation Social Stimuli P50MH100023 · NIMH · EMORY UNIVERSITY · PI YOUNG, LARRY J · 2013 to 2022
$21.8M
Neurotrophic and ontogenic factors in medial orbitofrontal cortical functionR01DA044297 · NIDA · EMORY UNIVERSITY · PI Shannon Leigh Gourley · 2018 to 2026
$3.7M
NIDA NIH HHS DA044297NIDA NIH HHS R01 DA044297NIH HHS P51 OD011132NIH Office of the Director OD011132NIMH NIH HHS MH100023NIMH NIH HHS P50 MH100023
6 · The paper itself

Abstract

Recognizing reward-related stimuli is crucial for survival. Neuronal projections from the basolateral amygdala (BLA) to the nucleus accumbens (NAc) play an important role in processing reward-related cues. Previous studies revealed synchronization between distant brain regions in reward-sensitive neurocircuits; however, whether the NAc synchronizes with the BLA is unknown. Here, we recorded local field potentials simultaneously from the BLA and NAc of rats during social preference tests and an appetitive conditioning test in which explicit stimuli were associated with food. BLA-NAc coherence in the theta band (5-8 Hz) increased in response to food-associated cues. Meanwhile, the modulatory strength of theta-high gamma (50-110 Hz) phase-amplitude cross-frequency coupling (PAC) in the NAc decreased. Importantly, both of these neuromodulations disappeared upon extinction. In contrast, both theta and gamma power oscillations in each region increased in the presence of social conspecifics or contexts associated with conspecifics, but coherence did not change. To potentially disrupt behavior and associated neural activity, a subgroup of rats was exposed prenatally to valproic acid (VPA), which has been shown to disrupt transcriptome and excitatory/inhibitory balance in the amygdala. VPA-exposed rats demonstrated impulsive-like behavior, but VPA did not affect BLA-NAc coherence. These findings reveal changes in BLA-NAc coherence in response to select reward-related stimuli (i.e., food-predictive cues); the differences between the tasks used here could shed light onto the functional nature of BLA-NAc coherence and are discussed.

Indexed as

RewardAnimalsAppetitive BehaviorBasolateral Nuclear ComplexBrain WavesConditioning, ClassicalExtinction, PsychologicalFemaleNeural PathwaysNucleus AccumbensRats, Sprague-DawleySocial BehaviorAppetitive conditioningCross-frequency couplingGammaNeural oscillationThetaValproateVentral striatum

Identifiers

PMID32556583
PMCPMC7405940
OpenAlexW3035847479

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.