Evidence map›Paper›PMID 30594547›Full record

ArticleBrain research2019

Early life stress alters opioid receptor mRNA levels within the nucleus accumbens in a sex-dependent manner.

Liza Chang, Stacey L Kigar, Jasmine H Ho, Amelia Cuarenta, Haley C Gunderson, Brian A Baldo, Vaishali P Bakshi, Anthony P Auger

Open access · greenAbstract read
In one paragraph

Article in Brain research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 18% 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, 33 citations in OpenAlex.

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  4. Father's care uniquely influences male neurodevelopment.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  12. Developmental Trajectories of Anhedonia in Preclinical Models.Current topics in behavioral neurosciences · 2022
    Article
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  14. Article
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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

8 authors at 1 institution in 1 country.

Liza ChangDepartment of Psychology, University of Wisconsin-Madison, United States. Electronic address: lchang9@wisc.edu.
Stacey L KigarMolecular and Cellular Pharmacology Training Program, University of Wisconsin-Madison, United States.
Jasmine H HoDepartment of Psychology, University of Wisconsin-Madison, United States.
Amelia CuarentaDepartment of Psychology, University of Wisconsin-Madison, United States.
Haley C GundersonDepartment of Psychology, University of Wisconsin-Madison, United States.
Brian A BaldoDepartment of Psychiatry, University of Wisconsin-Madison, United States; Neuroscience Training Program, University of Wisconsin-Madison, United States.
Vaishali P BakshiDepartment of Psychiatry, University of Wisconsin-Madison, United States; Neuroscience Training Program, University of Wisconsin-Madison, United States.
Anthony P AugerDepartment of Psychology, University of Wisconsin-Madison, United States; Neuroscience Training Program, University of Wisconsin-Madison, United States. Electronic address: apauger@wisc.edu.
University of Wisconsin–Madison · US

Funding

Training Program In Molecular AND Cellular PharmacologyT32GM008688 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI AUDHYA, ANJON · 1998 to 2020
$6.0M
NIGMS NIH HHS T32 GM008688
6 · The paper itself

Abstract

Early life stress (ELS) strongly impacts mental health, but little is known about its interaction with biological sex and postnatal development to influence risk and resilience to psychopathologies. A number of psychiatric disorders, such as social anhedonia and drug addiction, involve dysfunctional opioid signaling; moreover, there is evidence for differential central opioid function in males vs. females. The present study examined opioid receptor gene expression in the nucleus accumbens (NAc) and amygdala of male and female rats subjected to a neonatal predator odor exposure (POE) paradigm to model ELS. Brain tissue was collected at two developmental time points: neonatal and juvenile. Results showed that, following the neonatal POE experience, opioid receptor mRNA levels in the NAc were differentially regulated at the neonatal and juvenile time points. POE downregulated neonatal mu- and kappa-opioid receptor mRNA levels in neonatal females, but upregulated mu- and delta-opioid receptor mRNA levels in juvenile females. Intriguingly, POE had no significant effect on NAc opioid receptor mRNA levels in males at either time point, indicating that the impact of POE on opioid system development is sex-dependent. Finally, POE failed to alter amygdalar opioid receptor gene expression in either sex at either time-point. The spatiotemporally- and sex-specific impact of ELS within the developing brain may confer differential risk or resilience for males and females to develop atypical opioid-regulated behaviors associated with conditions such as depression and addiction.

Indexed as

Sex CharacteristicsAmygdalaAnimalsDown-RegulationFemaleMaleNucleus AccumbensRats, Sprague-DawleyReceptors, OpioidReceptors, Opioid, deltaReceptors, Opioid, kappaReceptors, Opioid, muRNA, MessengerStress, PsychologicalUp-RegulationReceptors, OpioidReceptors, Opioid, deltaReceptors, Opioid, kappaReceptors, Opioid, muRNA, MessengerAmygdalaDevelopmentEarly life stressNucleus accumbensOpioidsSex differences

Identifiers

PMID30594547
PMCPMC6701935
OpenAlexW2906708625

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.