Evidence map›Paper›PMID 29931501›Full record

ArticleJournal of molecular neuroscience : MN2018

In Vivo and In Vitro Neuronal Plasticity Modulation by Epigenetic Regulators.

Melisa C Monteleone, María Eugenia Pallarés, Silvia C Billi, Marta C Antonelli, Marcela A Brocco

Abstract read
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In one paragraph

Article in Journal of molecular neuroscience : MN, 2018. 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
0.3field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
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

5 authors at 2 institutions in 1 country.

Melisa C MonteleoneInstituto de Investigaciones Biotecnológicas - Instituto Tecnológico de Chascomús (IIB-INTECH), Universidad Nacional de San Martín, Consejo Nacional de Investigaciones Científicas y Técnicas (UNSAM-CONICET), Av. 25 de Mayo y Francia, CP: 1650, San Martín, Buenos Aires, Argentina.
María Eugenia PallarésInstituto de Biología Celular y Neurociencias "Prof. Eduardo De Robertis," Facultad de Medicina, Universidad de Buenos Aires, Paraguay 2155, 3°Piso, C1121ABG, Buenos Aires, Argentina.
Silvia C BilliInstituto de Investigaciones Biotecnológicas - Instituto Tecnológico de Chascomús (IIB-INTECH), Universidad Nacional de San Martín, Consejo Nacional de Investigaciones Científicas y Técnicas (UNSAM-CONICET), Av. 25 de Mayo y Francia, CP: 1650, San Martín, Buenos Aires, Argentina.
Marta C AntonelliInstituto de Biología Celular y Neurociencias "Prof. Eduardo De Robertis," Facultad de Medicina, Universidad de Buenos Aires, Paraguay 2155, 3°Piso, C1121ABG, Buenos Aires, Argentina.
Marcela A BroccoInstituto de Investigaciones Biotecnológicas - Instituto Tecnológico de Chascomús (IIB-INTECH), Universidad Nacional de San Martín, Consejo Nacional de Investigaciones Científicas y Técnicas (UNSAM-CONICET), Av. 25 de Mayo y Francia, CP: 1650, San Martín, Buenos Aires, Argentina. mbrocco@iib.unsam.edu.ar.ORCID http://orcid.org/0000-0002-7120-0814
Consejo Nacional de Investigaciones Científicas y Técnicas · ARUniversidad de Buenos Aires · AR

Funding

Fondo para la Investigación Científica y Tecnológica 1093-2014Fondo para la Investigación Científica y Tecnológica PICT 0807-2011Universidad de San Martin 2014-2015
6 · The paper itself

Abstract

Prenatal stress (PS) induces molecular changes that alter neural connectivity, increasing the risk for neuropsychiatric disorders. Here we analyzed -in the hippocampus of adult rats exposed to PS- the epigenetic signature mediating the PS-induced neuroplasticity changes. Furthermore, using cultured hippocampal neurons, we investigated the effects on neuroplasticity of an epigenetic modulator. PS induced significant modifications in the mRNA levels of stress-related transcription factor MEF2A, SUV39H1 histone methyltransferase, and TET1 hydroxylase, indicating that PS modifies gene expression through chromatin remodeling. In in vitro analysis, histone acetylation inhibition with apicidin increased filopodium density, suggesting that the external regulation of acetylation levels might modulate neuronal morphology. These results offer a way to enhance neural connectivity that could be considered to revert PS effects.

Indexed as

Epigenesis, GeneticHistone CodeNeuronal PlasticityAnimalsCells, CulturedDioxygenasesFemaleHippocampusHistone Deacetylase InhibitorsMaleMEF2 Transcription FactorsMethyltransferasesNeurogenesisNeuronsPeptides, CyclicPregnancyapicidinDioxygenasesHistone Deacetylase InhibitorsMEF2A protein, ratMEF2 Transcription FactorsMethyltransferasesPeptides, CyclicRepressor ProteinsSuv39h1 protein, ratTET1 protein, ratGPM6AHistone deacetylase inhibitorsHydroxymethylationMEF2APrimary hippocampal neuronsRat

Identifiers

PMID29931501
OpenAlexW2808736049

What OpenQuestion holds

Textmetadata
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.