Evidence map›Paper›PMID 39808339›Full record

ArticlePsychopharmacology2025

Poly ADP-ribosylation regulates Arc expression and promotes adaptive stress-coping.

Eliyahu Dahan, Leah Pergamenshik, Tze'ela Taub, Arthur Vovk, Jade Manier, Raphael Avneri, Elad Lax

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Article in Psychopharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Eliyahu Dahan *Department of Molecular Biology, Ariel University, Ariel, Israel.
Leah Pergamenshik *Department of Molecular Biology, Ariel University, Ariel, Israel.
Tze'ela TaubDepartment of Molecular Biology, Ariel University, Ariel, Israel.
Arthur VovkDepartment of Molecular Biology, Ariel University, Ariel, Israel.
Jade ManierDepartment of Molecular Biology, Ariel University, Ariel, Israel.
Raphael AvneriDepartment of Molecular Biology, Ariel University, Ariel, Israel.
Elad LaxDepartment of Molecular Biology, Ariel University, Ariel, Israel. eladl@ariel.ac.il.ORCID http://orcid.org/0000-0002-0310-0520

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleRapid adaptation to stressful events is essential for survival and requires acute stress response and stress-coping strategy. However, the molecular mechanisms that govern this coping strategy have yet to be fully discovered.

objectivesThis study aims to investigate the effects of poly ADP-ribosylation (PARylation) on stress-coping strategies following acute stress and to identify the target genes influenced by Parp1-induced histone PARylation.

methodsMice were subjected to a forced swim test, a well-established acute stress paradigm, to evaluate cortical PARylation and assess the expression of activity-dependent genes. The pharmacological inhibition of Parp1 was conducted using ABT888 (Veliparib) to determine its effects on stress-coping behavior and related molecular changes.

resultsThe forced swim test increased cortical PARylation and upregulated the expression of activity-dependent genes. Systemic inhibition of Parp1 with ABT888 led to impaired stress-coping behavior, evidenced by a reduced immobility response during a subsequent forced swim test done 24 hours later. This impairment was associated with decreased chromatin PARylation and histone H4 acetylation at the Arc promoter and reduced Arc expression observed one hour after Parp1 inhibition.

conclusionOur findings indicate that chromatin PARylation at the Arc promoters regulates histone H4 acetylation and Arc gene expression, and a subsequent impact on successful stress-coping behavior in response to acute stress.

Indexed as

Adaptation, PsychologicalCytoskeletal ProteinsNerve Tissue ProteinsPoly ADP RibosylationStress, PsychologicalAcetylationAnimalsBenzimidazolesGene Expression RegulationHistonesMaleMiceMice, Inbred C57BLPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) Polymerasesactivity regulated cytoskeletal-associated proteinBenzimidazolesCytoskeletal ProteinsHistonesNerve Tissue ProteinsParp1 protein, mousePoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) PolymerasesveliparibActivity-dependent genesAcute stressImmediate-early genesPoly ADP-ribosylationStress adaptationStress coping

Identifiers

PMID39808339
PMCPMC11890342

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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.