Evidence map›Paper›PMID 26670281›Full record

ArticleTranslational psychiatry2015

Brain plasticity and cognitive functions after ethanol consumption in C57BL/6J mice.

E Stragier, V Martin, E Davenas, C Poilbout, R Mongeau, R Corradetti, L Lanfumey

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

38 citing papers in PubMed, 77 citations in OpenAlex.

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  11. DNA Methylation in Alcohol Use Disorder.International journal of molecular sciences · 2023
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  16. Chemogenetic stimulation of the GPharmacology research & perspectives · 2021
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  17. Article
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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 2 institutions in 2 countries.

E StragierCentre de Psychiatrie et Neurosciences, INSERM UMR 894, Paris, France.
V MartinCentre de Psychiatrie et Neurosciences, INSERM UMR 894, Paris, France.
E DavenasCentre de Psychiatrie et Neurosciences, INSERM UMR 894, Paris, France.
C PoilboutCentre de Psychiatrie et Neurosciences, INSERM UMR 894, Paris, France.
R MongeauUniversité Paris Descartes, UMR S894, Paris, France.
R CorradettiDepartment of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy.ORCID http://orcid.org/0000-0002-2588-0484
L LanfumeyCentre de Psychiatrie et Neurosciences, INSERM UMR 894, Paris, France.
Délégation Paris 5 · FRUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute or chronic administrations of high doses of ethanol in mice are known to produce severe cognitive deficits linked to hippocampal damage. However, we recently reported that chronic and moderate ethanol intake in C57BL/6J mice induced chromatin remodeling within the Bdnf promoters, leading to both enhanced brain-derived neurotrophic factor (BDNF) expression and hippocampal neurogenesis under free-choice protocol. We performed here a series of cellular and behavioral studies to analyze the consequences of these modifications. We showed that a 3-week chronic free-choice ethanol consumption in C57BL/6J mice led to a decrease in DNA methylation of the Bdnf gene within the CA1 and CA3 subfields of the hippocampus, and upregulated hippocampal BDNF signaling pathways mediated by ERK, AKT and CREB. However, this activation did not affect long-term potentiation in the CA1. Conversely, ethanol intake impaired learning and memory capacities analyzed in the contextual fear conditioning test and the novel object recognition task. In addition, ethanol increased behavioral perseveration in the Barnes maze test but did not alter the mouse overall spatial capacities. These data suggested that in conditions of chronic and moderate ethanol intake, the chromatin remodeling leading to BDNF signaling upregulation is probably an adaptive process, engaged via epigenetic regulations, to counteract the cognitive deficits induced by ethanol.

Indexed as

AnimalsBehavior, AnimalCentral Nervous System DepressantsCognitionEthanolHippocampusImmunoblottingMaleMiceMice, Inbred C57BLModels, AnimalNeuronal PlasticityPolymerase Chain ReactionCentral Nervous System DepressantsEthanol

Identifiers

PMID26670281
PMCPMC5068583
OpenAlexW2211943037

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.