Evidence map›Paper›PMID 26032436›Full record

ArticleNeuropharmacology2015

Prenatal stress, regardless of concurrent escitalopram treatment, alters behavior and amygdala gene expression of adolescent female rats.

David E Ehrlich, Gretchen N Neigh, Chase H Bourke, Christina L Nemeth, Rimi Hazra, Steven J Ryan, Sydney Rowson, Nesha Jairam, Courtney A Sholar, Donald G Rainnie and 2 more

Abstract read
In one paragraph

Article in Neuropharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.6field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 47 citations in OpenAlex.

  1. A female-specific role for Slit1 in prenatal stress-induced depression vulnerability.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
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  3. Review
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  10. Review
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  12. Brain, behavior, & immunity - health · 2021
    Article
  13. Article
  14. Article
  15. Gestational Factors throughout Fetal Neurodevelopment: The Serotonin Link.International journal of molecular sciences · 2020
    Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article
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

12 authors at 3 institutions in 1 country.

David E EhrlichDept. of Psychiatry and Behavioral Sci., Atlanta, GA, USA; Division of Behavioral Neurosci. and Psychiatric Disorders, Yerkes National Primate Research Center, Atlanta, GA, USA.
Gretchen N NeighDept. of Psychiatry and Behavioral Sci., Atlanta, GA, USA; Dept. of Physiology, Emory University, Atlanta, GA, USA. Electronic address: gretchen.neigh@emory.edu.
Chase H BourkeDept. of Psychiatry and Behavioral Sci., Atlanta, GA, USA.
Christina L NemethDept. of Physiology, Emory University, Atlanta, GA, USA.
Rimi HazraDept. of Psychiatry and Behavioral Sci., Atlanta, GA, USA; Division of Behavioral Neurosci. and Psychiatric Disorders, Yerkes National Primate Research Center, Atlanta, GA, USA.
Steven J RyanDept. of Psychiatry and Behavioral Sci., Atlanta, GA, USA; Division of Behavioral Neurosci. and Psychiatric Disorders, Yerkes National Primate Research Center, Atlanta, GA, USA.
Sydney RowsonDept. of Psychiatry and Behavioral Sci., Atlanta, GA, USA.
Nesha JairamDept. of Psychiatry and Behavioral Sci., Atlanta, GA, USA.
Courtney A SholarDept. of Psychiatry and Behavioral Sci., Atlanta, GA, USA.
Donald G RainnieDept. of Psychiatry and Behavioral Sci., Atlanta, GA, USA; Division of Behavioral Neurosci. and Psychiatric Disorders, Yerkes National Primate Research Center, Atlanta, GA, USA.
Zachary N StoweDepartment of Psychiatry, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Michael J OwensDept. of Psychiatry and Behavioral Sci., Atlanta, GA, USA.
Behavioral Pharma (United States) · USEmory University · USUniversity of Arkansas for Medical Sciences · 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
The Impact of Maternal Depression, Anxiety, and StressP50MH077928 · NIMH · EMORY UNIVERSITY · PI OWENS, MICHAEL JOSEPH · 2007 to 2011
$9.6M
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
Graduate Training in the Pharmacological StudiesT32GM008602 · NIGMS · EMORY UNIVERSITY · PI HALL, RANDY A. · 1996 to 2021
$5.1M
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 P51 RR000165NCRR NIH HHS RR-00165NIGMS NIH HHS T32 GM008602NIGMS NIH HHS T32-GM008602NIH HHS P51 OD011132NIMH NIH HHS F31 MH090729NIMH NIH HHS MH-069852NIMH NIH HHS MH-077928NIMH NIH HHS MH-090729NIMH NIH HHS P50 MH077928NIMH NIH HHS R01 MH069852NINDS NIH HHS T32 NS096050
6 · The paper itself

Abstract

Depression during pregnancy has been linked to in utero stress and is associated with long-lasting symptoms in offspring, including anxiety, helplessness, attentional deficits, and social withdrawal. Depression is diagnosed in 10-20% of expectant mothers, but the impact of antidepressant treatment on offspring development is not well documented, particularly for females. Here, we used a prenatal stress model of maternal depression to test the hypothesis that in utero antidepressant treatment could mitigate the effects of prenatal stress. We also investigated the effects of prenatal stress and antidepressant treatment on gene expression related to GABAergic and serotonergic neurotransmission in the amygdala, which may underlie behavioral effects of prenatal stress. Nulliparous female rats were implanted with osmotic minipumps delivering clinically-relevant concentrations of escitalopram and mated. Pregnant dams were exposed to 12 days of mixed-modality stressors, and offspring were behaviorally assessed in adolescence (postnatal day 28) and adulthood (beyond day 90) to determine the extent of behavioral change. We found that in utero stress exposure, regardless of escitalopram treatment, increased anxiety-like behavior in adolescent females and profoundly influenced amygdala expression of the chloride transporters KCC2 and NKCC1, which regulate GABAergic function. In contrast, prenatal escitalopram exposure alone elevated amygdala expression of 5-HT1A receptors. In adulthood, anxiety-like behavior returned to baseline and gene expression effects in the amygdala abated, whereas deficits emerged in novel object recognition for rats exposed to stress during gestation. These findings suggest prenatal stress causes age-dependent deficits in anxiety-like behavior and amygdala function in female offspring, regardless of antidepressant exposure.

Indexed as

Prenatal Exposure Delayed EffectsAmygdalaAnimalsAnxietyCitalopramCorticosteroneDisease Models, AnimalEstradiolFemalegamma-Aminobutyric AcidGene ExpressionK Cl- CotransportersMemory DisordersPregnancyRats, Sprague-DawleyReceptor, Serotonin, 5-HT1ACitalopramCorticosteroneEstradiolgamma-Aminobutyric AcidK Cl- CotransportersReceptor, Serotonin, 5-HT1ASelective Serotonin Reuptake InhibitorsSlc12a2 protein, ratSolute Carrier Family 12, Member 2SymportersAntidepressantAnxietyFemaleGABAPrenatal stressSerotonin

Identifiers

PMID26032436
PMCPMC4537355
OpenAlexW430646550

What OpenQuestion holds

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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.