Evidence map›Paper›PMID 38101612›Full record

ArticleNeuroscience letters2024

Acute restraint stress regulates brain DNMT3a and promotes defensive behaviors in male rats.

Richard L Spinieli, Rafael Cazuza, Amanda J Sales, Ruither Carolino, Janete A Franci, Maral Tajerian, Christie R A Leite-Panissi

Open access · hybridAbstract read
In one paragraph

Article in Neuroscience letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

4 citing papers in PubMed, 15 citations in OpenAlex.

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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

7 authors at 3 institutions in 2 countries.

Richard L SpinieliDepartment of Psychology, School of Philosophy, Science and Literature of Ribeirão Preto of the University of São Paulo, Brazil. Electronic address: rspiniel@bidmc.harvard.edu.
Rafael CazuzaDepartment of Psychology, School of Philosophy, Science and Literature of Ribeirão Preto of the University of São Paulo, Brazil.
Amanda J SalesDepartment of Pharmacology, Medical School of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.
Ruither CarolinoDepartment of Basic and Oral Biology, Dental School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Janete A FranciDepartment of Basic and Oral Biology, Dental School of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Maral TajerianDepartment of Biology, Queens College, City University of New York, Flushing, NY, United States; The Graduate Center, City University of New York, New York, NY, United States.
Christie R A Leite-PanissiDepartment of Psychology, School of Philosophy, Science and Literature of Ribeirão Preto of the University of São Paulo, Brazil. Electronic address: christie@usp.br.
Universidade de São Paulo · BRQueens College, CUNY · USUniversidade de Ribeirão Preto · BR

Funding

Hippocampal Extracellular Matrix Regulates Glia-Neuron Crosstalk after InjurySC2GM135114 · NIGMS · QUEENS COLLEGE · PI TAJERIAN, MARAL · 2020 to 2022
$462k
NIGMS NIH HHS SC2 GM135114
6 · The paper itself

Abstract

Depending on its duration and severity, stress may contribute to neuropsychiatric diseases such as depression and anxiety. Studies have shown that stress impacts the hypothalamic-pituitary-adrenal (HPA) axis, but its downstream molecular, behavioral, and nociceptive effects remain unclear. We hypothesized that a 2-hour single exposure to acute restraint stress (ARS) activates the HPA axis and changes DNA methylation, a molecular mechanism involved in the machinery of stress regulation. We further hypothesized that ARS induces anxiety-like and risk assessment behavior and alters nociceptive responses in the rat. We employed biochemical (radioimmunoassay for corticosterone; global DNA methylation by enzyme immunoassay and western blot for DNMT3a expression in the amygdala, ventral hippocampus, and prefrontal cortex) and behavioral (elevated plus maze and dark-light box for anxiety and hot plate test for nociception) tests in adult male Wistar rats exposed to ARS or handling (control). All analyses were performed 24 h after ARS or handling. We found that ARS increased corticosterone levels in the blood, increased the expression of DNMT3a in the prefrontal cortex, promoted anxiety-like and risk assessment behaviors in the elevated plus maze, and increased the nociceptive threshold observed in the hot plate test. Our findings suggest that ARS might be a helpful rat model for studying acute stress and its effects on physiology, epigenetic machinery, and behavior.

Indexed as

CorticosteroneHypothalamo-Hypophyseal SystemAnimalsAnxietyBrainMalePituitary-Adrenal SystemRatsRats, WistarRestraint, PhysicalStress, PsychologicalCorticosteroneAcute restraint stressAnxiety-like behaviorsDNA methylationPrefrontal cortex

Identifiers

PMID38101612
PMCPMC10947420
OpenAlexW4389704845

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.