Evidence map›Paper›PMID 27733613›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

Alcohol Regulates BK Surface Expression via Wnt/β-Catenin Signaling.

Cristina Velázquez-Marrero, Alexandra Burgos, José O García, Stephanie Palacio, Héctor G Marrero, Alexandra Bernardo, Juliana Pérez-Laspiur, Marla Rivera-Oliver, Garrett Seale, Steven N Treistman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Potassium Channels and Their Potential Roles in Substance Use Disorders.International journal of molecular sciences · 2021
    Review
  7. Article
  8. Review
  9. Article
  10. Glycogen synthase kinase 3 beta regulates ethanol consumption and is a risk factor for alcohol dependence.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
  11. Article
  12. Review
  13. 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

10 authors at 1 institution in 1 country.

Cristina Velázquez-MarreroInstitute of Neurobiology, University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico 00901, Steven.Treistman@upr.edu Cristina.Velazquez1@upr.edu.ORCID 0000-0002-3784-9791
Alexandra BurgosInstitute of Neurobiology, University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico 00901, University of Puerto Rico Río Piedras Campus, San Juan, Puerto Rico 00931.
José O GarcíaInstitute of Neurobiology, University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico 00901, University of Puerto Rico Natural Sciences Department, Carolina Campus, San Juan, Puerto Rico 00984, and.ORCID 0000-0002-6349-0583
Stephanie PalacioInstitute of Neurobiology, University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico 00901.ORCID 0000-0003-3706-5628
Héctor G MarreroInstitute of Neurobiology, University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico 00901.ORCID 0000-0001-9387-5524
Alexandra BernardoInstitute of Neurobiology, University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico 00901.ORCID 0000-0001-7384-6187
Juliana Pérez-LaspiurRCMI Translational Proteomics Center University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico 00936.
Marla Rivera-OliverInstitute of Neurobiology, University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico 00901, University of Puerto Rico Río Piedras Campus, San Juan, Puerto Rico 00931.
Garrett SealeInstitute of Neurobiology, University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico 00901.ORCID 0000-0002-7159-5131
Steven N TreistmanInstitute of Neurobiology, University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico 00901, Steven.Treistman@upr.edu Cristina.Velazquez1@upr.edu.
University of Puerto Rico, Medical Sciences Campus · PR

Funding

The Role of Sensory Input to Mammalian Locomotion After the Loss of supraspinal.P20GM103642 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI LASALDE-DOMINICCI, JOSE ANTONIO · 2013 to 2023
$20.6M
TRANSLATIONAL PROTEOMICS CENTERG12MD007600 · NIMHD · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI FERNANDEZ-REPOLLET, EMMA · 2012 to 2016
$11.0M
miRNA Regulation of Gene Expression in Alcohol Tolerance and WithdrawalR01AA017920 · NIAAA · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI PIETRZYKOWSKI, ANDRZEJ ZBIGNIEW, TREISTMAN, STEVEN N · 2009 to 2013
$2.0M
NIAAA NIH HHS R01 AA017920NIGMS NIH HHS P20 GM103642NIMHD NIH HHS G12 MD007600
6 · The paper itself

Abstract

It has been suggested that drug tolerance represents a form of learning and memory, but this has not been experimentally established at the molecular level. We show that a component of alcohol molecular tolerance (channel internalization) from rat hippocampal neurons requires protein synthesis, in common with other forms of learning and memory. We identify β-catenin as a primary necessary protein. Alcohol increases β-catenin, and blocking accumulation of β-catenin blocks alcohol-induced internalization in these neurons. In transfected HEK293 cells, suppression of Wnt/β-catenin signaling blocks ethanol-induced internalization. Conversely, activation of Wnt/β-catenin reduces BK current density. A point mutation in a putative glycogen synthase kinase phosophorylation site within the S10 region of BK blocks internalization, suggesting that Wnt/β-catenin directly regulates alcohol-induced BK internalization via glycogen synthase kinase phosphorylation. These findings establish de novo protein synthesis and Wnt/β-catenin signaling as critical in mediating a persistent form of BK molecular alcohol tolerance establishing a commonality with other forms of long-term plasticity. SIGNIFICANCE STATEMENT: Alcohol tolerance is a key step toward escalating alcohol consumption and subsequent dependence. Our research aims to make significant contributions toward novel, therapeutic approaches to prevent and treat alcohol misuse by understanding the molecular mechanisms of alcohol tolerance. In our current study, we identify the role of a key regulatory pathway in alcohol-induced persistent molecular changes within the hippocampus. The canonical Wnt/β-catenin pathway regulates BK channel surface expression in a protein synthesis-dependent manner reminiscent of other forms of long-term hippocampal neuronal adaptations. This unique insight opens the possibility of using clinically tested drugs, targeting the Wnt/β-catenin pathway, for the novel use of preventing and treating alcohol dependency.

Indexed as

Amino Acid SequenceAnimalsbeta CateninCentral Nervous System DepressantsDrug ToleranceEthanolGlycogen Synthase KinasesHEK293 CellsHumansLarge-Conductance Calcium-Activated Potassium ChannelsNeuronal PlasticityNeuronsPhosphorylationPoint MutationRatsWnt Signaling Pathwaybeta CateninCentral Nervous System DepressantsEthanolGlycogen Synthase KinasesLarge-Conductance Calcium-Activated Potassium Channelsbeta-cateninBKdownregulationEtOHtoleranceWnt

Identifiers

PMID27733613
PMCPMC5059430
OpenAlexW2530925364

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.