Evidence map›Paper›PMID 23906943›Full record

ArticleNeurotoxicology and teratology

Prenatal exposure to escitalopram and/or stress in rats produces limited effects on endocrine, behavioral, or gene expression measures in adult male rats.

Chase H Bourke, Zachary N Stowe, Gretchen N Neigh, Darin E Olson, Michael J Owens

Abstract read
In one paragraph

Article in Neurotoxicology and teratology. 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
3.9field-weighted citation impact, top 7% 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, 38 citations in OpenAlex.

  1. Review
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  6. Cortical Cross-Frequency Coupling Is Affected byFrontiers in neuroscience · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. ACS chemical neuroscience · 2019
    Article
  11. Review
  12. Article
  13. Review
  14. Of rodents and humans: A comparative review of the neurobehavioral effects of early life SSRI exposure in preclinical and clinical research.International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2016
    Review
  15. Article
  16. Article
  17. Review
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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 3 institutions in 1 country.

Chase H BourkeLaboratory of Neuropsychopharmacology, Department of Psychiatry and Behavioral Sciences, Emory University, Atlanta, GA, USA.
Zachary N Stowe
Gretchen N Neigh
Darin E Olson
Michael J Owens
Emory University · USAtlanta VA Medical Center · USUniversity of Arkansas for Medical Sciences · US

Funding

The Impact of Maternal Depression, Anxiety, and StressP50MH077928 · NIMH · EMORY UNIVERSITY · PI NEWPORT, DONALD JEFFREY · 2007 to 2011
$9.6M
Graduate and Postdoctoral Training in ToxicologyT32ES012870 · NIEHS · EMORY UNIVERSITY · PI Carmen Joseph Marsit · 2004 to 2026
$9.1M
REQUEST FOR JEOL TRANSMISSION ELECTRON MICROSCOPES10RR012870 · NCRR · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI JORDAN, MARY A · 1999 to 1999
–
Howard Hughes Medical Institute 5600672NCRR NIH HHS RR012870NIEHS NIH HHS ES12870NIMH NIH HHS MH77928NIMH NIH HHS P50 MH077928
6 · The paper itself

Abstract

Stress and/or antidepressants during pregnancy have been implicated in a wide range of long-term effects in the offspring. We investigated the long-term effects of prenatal stress and/or clinically relevant antidepressant exposure on male adult offspring in a model of the pharmacotherapy of maternal depression. Female Sprague-Dawley rats were implanted with osmotic minipumps that delivered clinically relevant exposure to the antidepressant escitalopram throughout gestation. Subsequently, pregnant females were exposed on gestational days 10-20 to a chronic unpredictable mild stress paradigm. The male offspring were analyzed in adulthood. Baseline physiological measurements were largely unaltered by prenatal manipulations. Behavioral characterization of the male offspring, with or without pre-exposure to an acute stressor, did not reveal any group differences. Prenatal stress exposure resulted in a faster return towards baseline following the peak response to an acute restraint stressor, but not an airpuff startle stressor, in adulthood. Microarray analysis of the hippocampus and hypothalamus comparing all treatment groups revealed no significantly-altered transcripts. Real time PCR of the hippocampus confirmed that several transcripts in the CRFergic, serotonergic, and neural plasticity pathways were unaffected by prenatal exposures. This stress model of maternal depression and its treatment indicate that escitalopram use and/or stress during pregnancy produced no alterations in our measures of male adult behavior or the transcriptome, however prenatal stress exposure resulted in some evidence for increased glucocorticoid negative feedback following an acute restraint stress. Study design should be carefully considered before implications for human health are ascribed to prenatal exposure to stress or antidepressant medication.

Indexed as

AnimalsAntidepressive Agents, Second-GenerationBehavior, AnimalCitalopramEndocrine GlandsFemaleHippocampusHypothalamusMalePregnancyPrenatal Exposure Delayed EffectsRatsStress, PsychologicalTranscriptomeAntidepressive Agents, Second-GenerationCitalopramACTHadrenocorticotropic hormonecorticotropin-releasing factorCRFGene expressiongestational day NGNHPAhypothalamic–pituitary–adrenalHypothalamic–pituitary–adrenal axisMicroarrayNeuropharmacologyPNDNpostnatal day NPrenatal antidepressant exposurePrenatal stressSAMsignificance analysis of microarray

Identifiers

PMID23906943
PMCPMC3795959
OpenAlexW2032803475

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.