Evidence map›Paper›PMID 30710108›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2019

Chronic adolescent stress sex-specifically alters the hippocampal transcriptome in adulthood.

Sydney A Rowson, Mandakh Bekhbat, Sean D Kelly, Elisabeth B Binder, Molly M Hyer, Gladys Shaw, Maria Alexis Bent, Georgia Hodes, Gregory Tharp, David Weinshenker and 2 more

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

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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

12 authors.

Sydney A RowsonMolecular and Systems Pharmacology Graduate Program, Emory University, Atlanta, GA, USA.
Mandakh BekhbatNeuroscience Graduate Program, Emory University, Atlanta, GA, USA.
Sean D KellyDepartment of Physiology, Emory University, Atlanta, GA, USA.
Elisabeth B BinderDepartment of Psychiatry & Behavioral Sciences, Emory University, Atlanta, GA, USA.
Molly M HyerDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, USA.
Gladys ShawDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, USA.
Maria Alexis BentDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, USA.
Georgia HodesDepartment of Neuroscience, Virginia Polytechnic Institute and State University, 1981 Kraft Drive, Blacksburg, VA, USA.ORCID http://orcid.org/0000-0002-1551-2178
Gregory TharpYerkes National Primate Research Center, Atlanta, GA, USA.
David WeinshenkerDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
Zhouhui QinDepartment of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA, USA.
Gretchen N NeighDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, VA, USA. gretchen.mccandless@vcuhealth.org.

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
Virginia Commonwealth University IRADCAK12GM093857 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI DANIEL C BULLARD, John J Ryan · 2010 to 2026
$7.0M
Virginia Commonwealth University Initiative for Maximizing Student DevelopmentR25GM090084 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI AKBARALI, HAMID I, LLOYD, JOYCE A. · 2010 to 2022
$5.2M
Graduate Training in the Pharmacological StudiesT32GM008602 · NIGMS · EMORY UNIVERSITY · PI HALL, RANDY A. · 1996 to 2021
$5.1M
Virginia Commonwealth University Postbaccalaureate Research Education ProgramR25GM089614 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI Rebecca Kelley Martin · 2010 to 2026
$4.9M
Adult Implications of Chronic Adolescent Stress: Mediators and ModifiersR01NR014886 · NINR · VIRGINIA COMMONWEALTH UNIVERSITY · PI NEIGH, GRETCHEN N · 2014 to 2018
$2.1M
NIGMS NIH HHS 2R25GM090084-09NIGMS NIH HHS K12 GM093857NIGMS NIH HHS R25 GM089614NIGMS NIH HHS R25 GM090084NIGMS NIH HHS T32 GM008602NIH HHS P51 OD011132NINR NIH HHS R01 NR014886U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) T32-GM008602U.S. Department of Health & Human Services | NIH | National Institute of Nursing Research (NINR) NR014886
6 · The paper itself

Abstract

Chronic adolescent stress alters behavior in a sex-specific manner at the end of adolescence and in adulthood. Although prolonged behavioral repercussions of chronic adolescent stress have been documented, the potential underlying mechanisms are incompletely understood. In this study we demonstrate that a history of chronic adolescent stress modified the adult stress response, as measured by corticosterone concentration, such that a history of chronic adolescent stress resulted in a blunted response to a novel acute stressor. In order to begin to address potential mechanistic underpinnings, we assessed the extent to which chronic adolescent stress impacted global DNA methylation. Reduced global hippocampal methylation was evident in females with a history of chronic adolescent stress; thus, it was possible that chronic adolescent stress altered global transcription in the whole hippocampi of adult male and female rats. In addition, because acute stress can stimulate a genomic response, we assessed the transcriptome following exposure to an acute novel stressor to determine the extent to which a history of chronic adolescent stress modifies the adult transcriptional response to an acute stressor in males and females. In addition to the reduction in global methylation, chronic adolescent stress resulted in distinct patterns of gene expression in the adult hippocampus that differentiated by sex. Furthermore, both sex and a history of chronic adolescent stress influenced the transcriptional response to an acute novel stressor in adulthood, suggesting both latent and functional effects of chronic adolescent stress at the level of gene transcription. Pathway analysis indicated that ESR1 and IFN-α may be particularly influential transcription factors mediating these transcriptional differences and suggest candidate mechanisms for future studies. Collectively, these studies demonstrate sex-specific and enduring effects of adolescent stress exposure that are more pronounced in females than in males.

Indexed as

Sex CharacteristicsAge FactorsAnimalsCorticosteroneDNA MethylationFemaleHippocampusMaleRats, WistarStress, PsychologicalTranscriptomeCorticosterone

Identifiers

PMID30710108
PMCPMC6785712

What OpenQuestion holds

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Registered trials

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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.