Evidence map›Paper›PMID 24240029›Full record

ArticleNeuroscience2014

Unpredictable neonatal stress enhances adult anxiety and alters amygdala gene expression related to serotonin and GABA.

E C Sarro, R M Sullivan, G Barr

Abstract read
In one paragraph

Article in Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

48 citing papers in PubMed, 80 citations in OpenAlex.

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  16. Brain, behavior, & immunity - health · 2021
    Article
  17. Interoception, Trait Anxiety, and the Gut Microbiome: A Cognitive and Physiological Model.Medical science monitor : international medical journal of experimental and clinical research · 2021
    Review
  18. Article
  19. 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

3 authors at 3 institutions in 1 country.

E C SarroChild Study Center, Center for Early Childhood Health & Development, Child & Adolescent Psychiatry, New York University School of Medicine, New York, NY 10010, United States; Emotional Brain Institute, Nathan Kline Institute, 140 Old Orangeburg Road, Orangeburg, NY 10962, United States. Electronic address: emma.sarro@nyumc.org.
R M SullivanChild Study Center, Center for Early Childhood Health & Development, Child & Adolescent Psychiatry, New York University School of Medicine, New York, NY 10010, United States; Emotional Brain Institute, Nathan Kline Institute, 140 Old Orangeburg Road, Orangeburg, NY 10962, United States.
G BarrThe Children's Hospital of Philadelphia, Department of Anesthesiology and Critical Care Medicine, Perelman School of Medicine at the University of Pennsylvania, United States.
Children's Hospital of Philadelphia · USFoundation for Child Development · USNathan Kline Institute for Psychiatric Research · US

Funding

Amygdala Gene Expression: Learning in a Sensitive PeriodR01MH080603 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI BARR, GORDON ALFRED · 2006 to 2010
$1.5M
NIMH NIH HHS MH80603NIMH NIH HHS R01 MH080603
6 · The paper itself

Abstract

Anxiety-related disorders are among the most common psychiatric illnesses, thought to have both genetic and environmental causes. Early-life trauma, such as abuse from a caregiver, can be predictable or unpredictable, each resulting in increased prevalence and severity of a unique set of disorders. In this study, we examined the influence of early unpredictable trauma on both the behavioral expression of adult anxiety and gene expression within the amygdala. Neonatal rats were exposed to unpaired odor-shock conditioning for 5 days, which produces deficits in adult behavior and amygdala dysfunction. In adulthood, we used the Light/Dark box test to measure anxiety-related behaviors, measuring the latency to enter the lit area and quantified urination and defecation. The amygdala was then dissected and a microarray analysis was performed to examine changes in gene expression. Animals that had received early unpredictable trauma displayed significantly longer latencies to enter the lit area and more defecation and urination. The microarray analysis revealed over-represented genes related to learning and memory, synaptic transmission and trans-membrane transport. Gene ontology and pathway analysis identified highly represented disease states related to anxiety phenotypes, including social anxiety, obsessive-compulsive disorders, post-traumatic stress disorder and bipolar disorder. Addiction-related genes were also overrepresented in this analysis. Unpredictable shock during early development increased anxiety-like behaviors in adulthood with concomitant changes in genes related to neurotransmission, resulting in gene expression patterns similar to anxiety-related psychiatric disorders.

Indexed as

AmygdalaAnimalsAnimals, NewbornAnxietyAnxiety DisordersConditioning, ClassicalElectroshockgamma-Aminobutyric AcidGene Expression RegulationGene OntologyMaleNeuropsychological TestsOdorantsOlfactory PerceptionRatsRats, Long-Evansgamma-Aminobutyric AcidSerotoninanxietyearly lifeIngenuity Pathways AnalysisIPAmicroarraypercentage of false predictionspfpPNpostnatalpost-traumatic stress disorderPTSTrodentstressunpredictable

Identifiers

PMID24240029
PMCPMC4050971
OpenAlexW1981586625

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.