Evidence map›Paper›PMID 39798835›Full record

ArticleNeuroscience2025

Peripubertal antagonism of corticotropin-releasing factor receptor 1 results in sustained changes in behavioral plasticity and the transcriptomic profile of the amygdala.

Julia Martz, Micah A Shelton, Tristen J Langen, Sakhi Srinivasan, Marianne L Seney, Amanda C Kentner

Abstract read
In one paragraph

Article in Neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Julia MartzSchool of Arts & Sciences, Health Psychology Program, Massachusetts College of Pharmacy and Health Sciences, Boston Massachusetts, 02115, United States.
Micah A SheltonDepartment of Psychiatry, University of Pittsburgh, 450 Technology Drive, Pittsburgh, PA, 15219, United States.
Tristen J LangenSchool of Arts & Sciences, Health Psychology Program, Massachusetts College of Pharmacy and Health Sciences, Boston Massachusetts, 02115, United States.
Sakhi SrinivasanSchool of Arts & Sciences, Health Psychology Program, Massachusetts College of Pharmacy and Health Sciences, Boston Massachusetts, 02115, United States.
Marianne L SeneyDepartment of Psychiatry, University of Pittsburgh, 450 Technology Drive, Pittsburgh, PA, 15219, United States.
Amanda C KentnerSchool of Arts & Sciences, Health Psychology Program, Massachusetts College of Pharmacy and Health Sciences, Boston Massachusetts, 02115, United States. Electronic address: amanda.kentner@mcphs.edu.

Funding

Sex-specific dendritic spine and microglia pathology in depressionR01MH120066 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SENEY, MARIANNE L · 2019 to 2023
$1.9M
The protective role of environmental enrichment on placental mediators of hypothalamic pituitary adrenal axis dysfunction in a prenatal inflammatory rat modelR15MH114035 · NIMH · MCPHS UNIVERSITY · PI KENTNER, AMANDA · 2018 to 2022
$788k
NIMH NIH HHS R01 MH120066NIMH NIH HHS R15 MH114035
6 · The paper itself

Abstract

Peripuberty is a significant period of neurodevelopment with long-lasting effects on the brain and behavior. Blocking type 1 corticotropin-releasing factor receptors (CRFR1) in neonatal and peripubertal rats attenuates detrimental effects of early-life stress on neural plasticity, behavior, and stress hormone action, long after exposure to the drug has ended. CRFR1 antagonism can also impact neural and behavioral development in the absence of stressful stimuli, suggesting sustained alterations under baseline conditions. To investigate this further, we administered the CRFR1 antagonist (CRFR1a) R121919 to young adolescent male and female rats across 4 days. Following each treatment, rats were tested for locomotion, social behavior, mechanical allodynia, or prepulse inhibition (PPI). Acute CRFR1 blockade immediately reduced PPI in peripubertal males, but not females. In adulthood, each assay was repeated without CRFR1a exposure to test for persistent effects of the adolescent treatment. Males continued to experience deficits in PPI while females displayed altered locomotion, PPI, and social behavior. The amygdala was collected to measure long-term effects on gene expression. In the adult amygdala, peripubertal CRFR1a induced alterations in pathways related to neural plasticity and stress in males. In females, pathways related to central nervous system myelination, cell junction organization, and glutamatergic regulation of synaptic transmission were affected. Understanding how acute exposure to neuropharmacological agents can have sustained impacts on brain and behavior, in the absence of further exposures, has important clinical implications for developing adolescents.

Indexed as

AmygdalaNeuronal PlasticityReceptors, Corticotropin-Releasing HormoneTranscriptomeAnimalsBehavior, AnimalCRF Receptor, Type 1FemaleLocomotionMalePrepulse InhibitionPyrimidinesRatsRats, Sprague-DawleySex CharacteristicsSocial BehaviorCRF Receptor, Type 1PyrimidinesR 121919Receptors, Corticotropin-Releasing HormoneAdolescenceAmygdalaCorticotropin releasing factorNeuroplasticityPubertyTranscriptomics

Identifiers

PMID39798835
PMCPMC11789919

What Socratic 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 Socratic graph.