Evidence map›Paper›PMID 32045935›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2020

Pubertal adversity alters chromatin dynamics and stress circuitry in the pregnant brain.

Kathleen E Morrison, Anthony B Cole, Patrick J Kane, Victoria E Meadows, Scott M Thompson, Tracy L Bale

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 23 citations in OpenAlex.

  1. Altered Postnatal Chromatin Development in the Nucleus Accumbens Primes Enduring Stress Sensitivity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
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  5. [Mechanisms by Which Paraventricular Hypothalamic Nucleus Participates in the Acupuncture Treatment of Diseases].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2025
    Review
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  11. Chemogenetic activation of CRF neurons as a model of chronic stress produces sex-specific physiological and behavioral effects.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  12. 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

6 authors at 1 institution in 1 country.

Kathleen E MorrisonDepartment of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA.ORCID http://orcid.org/0000-0002-3665-4757
Anthony B ColeDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Patrick J KaneDepartment of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA.
Victoria E MeadowsDepartment of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA.
Scott M ThompsonDepartment of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Tracy L BaleDepartment of Pharmacology, University of Maryland School of Medicine, Baltimore, MD, USA. tbale@som.umaryland.edu.
University of Maryland, Baltimore · US

Funding

Prepubertal Stress, Windows of Risk & Sex Bias for Affective DisturbanceP50MH099910 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI KIM, DEBORAH · 2012 to 2017
$6.5M
Paternal stress epigenetic programming of offspring neurodevelopmentR37MH108286 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BALE, TRACY L · 2015 to 2024
$6.2M
TRAINING PROGRAM IN INTEGRATIVE MEMBRANE BIOLOGYT32GM008181 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI RIZZO, MEGAN A, TRUDEAU, MATTHEW C · 1987 to 2022
$4.9M
Stress, Depression, Serotonin, and Plasticity of Excitatory TransmissionR01MH086828 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI THOMPSON, SCOTT M. · 2010 to 2019
$3.8M
Placental epigenetic mechanisms contributing to sex-specific impacts of maternal stress on fetal developmentR01HD097093 · NICHD · UNIVERSITY OF MARYLAND BALTIMORE · PI BALE, TRACY L · 2019 to 2023
$2.4M
Female preconception stress programming of offspring neurodevelopmentR01ES028202 · NIEHS · UNIVERSITY OF MARYLAND BALTIMORE · PI BALE, TRACY L · 2017 to 2021
$2.2M
Maternal stress and the vaginal microbiome: impacts on brain developmentR33MH104184 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BALE, TRACY L · 2016 to 2018
$1.9M
Role of hormonal state in programming effects of peripubertal stress in femalesR00HD091376 · NICHD · WEST VIRGINIA UNIVERSITY · PI MORRISON, KATHLEEN ELIZABETH · 2020 to 2022
$578k
Maternal stress and the vaginal microbiome: impacts on brain developmentR21MH104184 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI BALE, TRACY L · 2014 to 2015
$555k
Role of hormonal state in programming effects of peripubertal stress in femalesK99HD091376 · NICHD · UNIVERSITY OF MARYLAND BALTIMORE · PI MORRISON, KATHLEEN ELIZABETH · 2017 to 2018
$251k
NICHD NIH HHS K99 HD091376NICHD NIH HHS R00 HD091376NICHD NIH HHS R01 HD097093NIEHS NIH HHS R01 ES028202NIGMS NIH HHS T32 GM008181NIMH NIH HHS P50 MH099910NIMH NIH HHS R01 MH086828NIMH NIH HHS R21 MH104184NIMH NIH HHS R33 MH104184NIMH NIH HHS R37 MH108286
6 · The paper itself

Abstract

Women who have experienced adverse childhood events (ACEs) around puberty are at the greatest risk for neuropsychiatric disorders across the lifespan. This population is exceptionally vulnerable to neuropsychiatric disease presentation during the hormonally dynamic state of pregnancy. We previously established that chronic adversity around puberty in female mice significantly altered their HPA axis function specifically during pregnancy, modeling the effects of pubertal ACEs we also reported in women. We hypothesized that the pregnancy hormone, allopregnanolone, was involved in presentation of the blunted stress response phenotype by its interaction with the molecular programming that had occurred during pubertal adversity experience. Here, in adult mice previously stressed during puberty, allopregnanolone administration was sufficient to reproduce the decreased corticosterone response after acute stress. Examination of neuronal activation and the electrophysiological properties of CRF neurons in the paraventricular nucleus of the hypothalamus (PVN) found no significant changes in synaptic function that corresponded with the blunted HPA axis reactivity. However, at the chromatin level, utilization of ATAC-Seq profiling demonstrated a dramatic remodeling of DNA accessibility in the PVN following pubertal adversity. Altogether, these data establish a potential molecular mechanism whereby adversity during puberty can enact lasting transcriptional control that manifests only during a unique period of the lifespan where dynamic hormonal changes occur. These results highlight a biological process that may impart an increased risk for a highly vulnerable population, whereby pubertal programming of the PVN results in aberrant HPA axis responsiveness when exposed to the hormonal changes unique to pregnancy.

Indexed as

Hypothalamo-Hypophyseal SystemPituitary-Adrenal SystemAnimalsBrainChromatinCorticosteroneCorticotropin-Releasing HormoneFemaleMiceParaventricular Hypothalamic NucleusPregnancyStress, PsychologicalChromatinCorticosteroneCorticotropin-Releasing Hormone

Identifiers

PMID32045935
PMCPMC7297802
OpenAlexW3004720140

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.