Evidence map›Paper›PMID 28890345›Full record

ArticleNeuron2017

Prosapip1-Dependent Synaptic Adaptations in the Nucleus Accumbens Drive Alcohol Intake, Seeking, and Reward.

Sophie Laguesse, Nadege Morisot, Jung Hoon Shin, Feng Liu, Martin F Adrover, Samuel A Sakhai, Marcelo F Lopez, Khanhky Phamluong, William C Griffin, Howard C Becker and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Neuron, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

42 citing papers in PubMed, 65 citations in OpenAlex.

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  16. Alcohol and the brain: from genes to circuits.Trends in neurosciences · 2021
    Review
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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

13 authors at 4 institutions in 1 country.

Sophie LaguesseDepartment of Neurology, University of California, San Francisco, CA, USA.
Nadege MorisotDepartment of Neurology, University of California, San Francisco, CA, USA.
Jung Hoon ShinLaboratory on Neurobiology of Compulsive Behaviors, National Institute of Alcohol Abuse and Alcoholism, US National Institutes of Health, Bethesda, MD, USA.
Feng LiuDepartment of Neurology, University of California, San Francisco, CA, USA.
Martin F AdroverLaboratory on Neurobiology of Compulsive Behaviors, National Institute of Alcohol Abuse and Alcoholism, US National Institutes of Health, Bethesda, MD, USA.
Samuel A SakhaiDepartment of Neurology, University of California, San Francisco, CA, USA.
Marcelo F LopezCharleston Alcohol Research Center, Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, USA.
Khanhky PhamluongDepartment of Neurology, University of California, San Francisco, CA, USA.
William C GriffinCharleston Alcohol Research Center, Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, USA.
Howard C BeckerCharleston Alcohol Research Center, Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, USA; Department of Neurosciences, Medical University of South Carolina, Charleston, SC, USA; RHJ Department of Veterans Affairs Medical Center, Charleston, SC, USA.
Kevin J BenderDepartment of Neurology, University of California, San Francisco, CA, USA.
Veronica A AlvarezLaboratory on Neurobiology of Compulsive Behaviors, National Institute of Alcohol Abuse and Alcoholism, US National Institutes of Health, Bethesda, MD, USA.
Dorit RonDepartment of Neurology, University of California, San Francisco, CA, USA. Electronic address: dorit.ron@ucsf.edu.
University of California, San Francisco · USMedical University of South Carolina · USNational Institute on Alcohol Abuse and Alcoholism · USNational Institutes of Health · US

Funding

TREATING ETHANOL WITHDRAWAL WITH LORAZEPAM/NALTREXONEP50AA010761 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI HOWARD C. BECKER · 1996 to 2026
$46.8M
Synaptic mechanisms underlying reward seeking and compulsive drug useZIAAA000421 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI ALVAREZ, VERONICA A · 2009 to 2025
$23.1M
Vector, Transgenic, and Imaging CoreP50AA017072 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RON, DORIT · 2008 to 2017
$13.9M
Ethanol Dependence &Stress Effects on Ethanol DrinkingU01AA014095 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI HOWARD C. BECKER · 2003 to 2026
$9.0M
Mouse Chronic Intermittent Ethanol (CIE) CoreU01AA020929 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LOPEZ, MARCELO F. · 2012 to 2015
$1.5M
Mouse Chronic Intermittent Ethanol (CIE) CoreU24AA020929 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LOPEZ, MARCELO F. · 2016 to 2021
$1.1M
Role of BDNF in Stress Effects on Ethanol Dependence-Induced Escalated DrinkingI01BX000813 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI BECKER, HOWARD C. · 2011 to 2024
–
BLRD VA I01 BX000813Intramural NIH HHS ZIA AA000421NIAAA NIH HHS P50 AA010761NIAAA NIH HHS P50 AA017072NIAAA NIH HHS U01 AA014095NIAAA NIH HHS U01 AA020929NIAAA NIH HHS U24 AA020929
6 · The paper itself

Abstract

The mammalian target of rapamycin complex 1 (mTORC1), a transducer of local dendritic translation, participates in learning and memory processes as well as in mechanisms underlying alcohol-drinking behaviors. Using an unbiased RNA-seq approach, we identified Prosapip1 as a novel downstream target of mTORC1 whose translation and consequent synaptic protein expression are increased in the nucleus accumbens (NAc) of mice excessively consuming alcohol. We demonstrate that alcohol-dependent increases in Prosapip1 levels promote the formation of actin filaments, leading to changes in dendritic spine morphology of NAc medium spiny neurons (MSNs). We further demonstrate that Prosapip1 is required for alcohol-dependent synaptic localization of GluA2 lacking AMPA receptors in NAc shell MSNs. Finally, we present data implicating Prosapip1 in mechanisms underlying alcohol self-administration and reward. Together, these data suggest that Prosapip1 in the NAc is a molecular transducer of structural and synaptic alterations that drive and/or maintain excessive alcohol use.

Indexed as

RewardActin CytoskeletonAlcohol DrinkingAnimalsCarrier ProteinsDendritic SpinesDrug-Seeking BehaviorEthanolMaleMechanistic Target of Rapamycin Complex 1Membrane ProteinsMiceMultiprotein ComplexesNeuronal PlasticityNucleus AccumbensReceptors, AMPACarrier ProteinsEthanolglutamate receptor ionotropic, AMPA 2Mechanistic Target of Rapamycin Complex 1Membrane ProteinsMultiprotein ComplexesProSAPiP1 protein, mouseReceptors, AMPATOR Serine-Threonine KinasesActinAddictionAlcoholDendritic spinesmTORC1PlasticityProsapip1

Identifiers

PMID28890345
PMCPMC6014831
OpenAlexW2753236023

What OpenQuestion holds

Textmetadata
LicenceTDM
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.