Evidence map›Paper›PMID 25716930›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2015

Prenatal Stress Alters the Development of Socioemotional Behavior and Amygdala Neuron Excitability in Rats.

David E Ehrlich, Donald G Rainnie

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.6field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  15. Article
  16. Mast Cells, Stress, Fear and Autism Spectrum Disorder.International journal of molecular sciences · 2019
    Review
  17. Article
  18. Article
  19. Elevated intracellular NaJournal of neurochemistry · 2017
    Article
  20. Review
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

2 authors at 1 institution in 1 country.

David E EhrlichDivision of Behavioral Neuroscience and Psychiatric Disorders, Department of Psychiatry and Behavioral Sciences, Yerkes Research Center, Emory University School of Medicine, Atlanta, GA, USA.
Donald G RainnieDivision of Behavioral Neuroscience and Psychiatric Disorders, Department of Psychiatry and Behavioral Sciences, Yerkes Research Center, Emory University School of Medicine, Atlanta, GA, USA.ORCID 0000000307580530
Emory University · 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
YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI RENGARAJAN, JYOTHI · 1985 to 2011
$114.0M
Rolipram Revisited: New roles for PDE4 and AMPK in the etiology of affective disordersR01MH069852 · NIMH · EMORY UNIVERSITY · PI YOUNG, LARRY J · 2005 to 2020
$5.7M
Training In Systems And Integrative Biology NeuroscienceT32NS096050 · NINDS · EMORY UNIVERSITY · PI Yoland Smith · 2016 to 2026
$3.9M
Critical Periods in Development of Amygdala Inhibition: Effect of Prenatal StressF31MH090729 · NIMH · EMORY UNIVERSITY · PI EHRLICH, DAVID EDWARD · 2011 to 2013
$92k
NCRR NIH HHS RR 00165NIH HHS P51 OD011132NIMH NIH HHS F31 MH090729NIMH NIH HHS MH 069852NIMH NIH HHS MH 090729NIMH NIH HHS R01 MH069852NINDS NIH HHS T32 NS096050
6 · The paper itself

Abstract

Prenatal stress (PS) is a risk factor for neurodevelopmental disorders with diverse ages of onset and socioemotional symptoms. Some PS-linked disorders involve characteristic social deficits, such as autism spectrum disorders and schizophrenia, but PS also promotes anxiety disorders. We propose the diversity of symptoms following PS arises from perturbations to early brain development. To this end, we characterized the effects of PS on the developmental trajectory of physiology of the amygdala, a late-developing center for socioemotional control. We found that PS dampened socioemotional behavior and reduced amygdala neuron excitability in offspring during infancy (at postnatal days (P)10, 14, 17 and 21), preadolescence (day 28), and adulthood (day 60). PS offspring in infancy produced fewer isolation-induced vocalizations and in adulthood exhibited less anxiety-like behavior and deficits in social interaction. PS neurons had a more hyperpolarized resting membrane potential from infancy to adulthood and produced fewer action potentials. Moreover, adult amygdala neurons from PS animals expressed larger action potential afterhyperpolarizations and H-current relative to controls, further limiting excitability. Our results suggest that PS can suppress socioemotional behavior throughout development and produce age-specific alterations to amygdala physiology.

Indexed as

Prenatal Exposure Delayed EffectsAge FactorsAmygdalaAnalysis of VarianceAnimalsAnimals, NewbornDevelopmental DisabilitiesFemaleIn Vitro TechniquesMaleMembrane PotentialsNeuronsPatch-Clamp TechniquesPregnancyRatsRats, Sprague-Dawley

Identifiers

PMID25716930
PMCPMC4613602
OpenAlexW1965590153

What OpenQuestion holds

Textmetadata
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.