Evidence map›Paper›PMID 28957664›Full record

ArticleNeuron2017

HDAC5 and Its Target Gene, Npas4, Function in the Nucleus Accumbens to Regulate Cocaine-Conditioned Behaviors.

Makoto Taniguchi, Maria B Carreira, Yonatan A Cooper, Ana-Clara Bobadilla, Jasper A Heinsbroek, Nobuya Koike, Erin B Larson, Evan A Balmuth, Brandon W Hughes, Rachel D Penrod and 9 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 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

74 citing papers in PubMed, 122 citations in OpenAlex.

  1. Article
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  15. Article
  16. Epigenetics in Learning and Memory.Sub-cellular biochemistry · 2025
    Review
  17. Article
  18. Review
  19. Article
  20. Article

14 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 5 institutions in 1 country.

Makoto TaniguchiDepartments of Neuroscience and Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, SC 29425, USA; Department of Psychiatry, Harvard Medical School, McLean Hospital, Belmont, MA 02478, USA.
Maria B CarreiraDepartment of Psychiatry, Harvard Medical School, McLean Hospital, Belmont, MA 02478, USA; Neuroscience Graduate Program, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Yonatan A CooperDepartment of Brain and Cognitive Science, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Ana-Clara BobadillaDepartments of Neuroscience and Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
Jasper A HeinsbroekDepartments of Neuroscience and Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
Nobuya KoikeDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Erin B LarsonDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Evan A BalmuthDepartment of Psychiatry, Harvard Medical School, McLean Hospital, Belmont, MA 02478, USA.
Brandon W HughesDepartments of Neuroscience and Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
Rachel D PenrodDepartments of Neuroscience and Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, SC 29425, USA; Department of Psychiatry, Harvard Medical School, McLean Hospital, Belmont, MA 02478, USA.
Jaswinder KumarDepartment of Psychiatry, Harvard Medical School, McLean Hospital, Belmont, MA 02478, USA; Neuroscience Graduate Program, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Laura N SmithDepartment of Psychiatry, Harvard Medical School, McLean Hospital, Belmont, MA 02478, USA.
Daniel GuzmanDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Joseph S TakahashiDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Tae-Kyung KimDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Peter W KalivasDepartments of Neuroscience and Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
David W SelfDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Yingxi LinDepartment of Brain and Cognitive Science, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Christopher W CowanDepartments of Neuroscience and Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, SC 29425, USA; Department of Psychiatry, Harvard Medical School, McLean Hospital, Belmont, MA 02478, USA. Electronic address: cowanc@musc.edu.
Medical University of South Carolina · USThe University of Texas Southwestern Medical Center · USHarvard University · USMassachusetts Institute of Technology · USMcLean Hospital · US

Funding

TRANSGENIC COREP01DA008227 · NIDA · YALE UNIVERSITY · PI NESTLER, ERIC J. · 1993 to 2018
$28.1M
DRUG ABUSE TRAINING PROGRAMT32DA007288 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Christopher W Cowan, Rachel Penrod-Martin · 1991 to 2026
$11.8M
Role of Class IIa HDAC Target Genes in Opioid and Cocaine AddictionR01DA032708 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI COWAN, CHRISTOPHER W · 2013 to 2022
$3.8M
OPIOIDS, AMPHETAMINE &COCAIN IN DRUG ABUSER01DA003906 · NIDA · WASHINGTON STATE UNIVERSITY · PI KALIVAS, PETER W · 1985 to 2019
$3.6M
Transcriptional Mechanisms of Addiction-Related Neural PlasticityR01DA027664 · NIDA · UT SOUTHWESTERN MEDICAL CENTER · PI COWAN, CHRISTOPHER W · 2011 to 2021
$3.6M
Regulation of Addictive Behavior by Dopamine SignalingR01DA010460 · NIDA · UT SOUTHWESTERN MEDICAL CENTER · PI SELF, DAVID W · 2002 to 2012
$3.1M
COCAINE, OPIOIDS AND DRUG ABUSER37DA003906 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KALIVAS, PETER W · 2000 to 2009
$3.0M
The Role of GABAergic Synaptic Plasticity in Neural Circuit FunctionsR01MH091220 · NIMH · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LIN, YINGXI · 2010 to 2014
$2.1M
The epigenetic mechanism of enhancer RNA in behavioral plasticityR01NS085418 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI KIM, TAE-KYUNG · 2013 to 2017
$1.7M
INTRACELLULAR MECHANISMS OF DRUG REWARD AND ADDICTIONR29DA010460 · NIDA · YALE UNIVERSITY · PI SELF, DAVID W · 1996 to 2002
$303k
Epigenetic mechanimsms in cocaine rewardF32DA036319 · NIDA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI PENROD-MARTIN, RACHEL · 2014 to 2016
$164k
The role and regulation of HDAC5 in cocaine addictionF31DA035073 · NIDA · MCLEAN HOSPITAL · PI CARREIRA, MARIA B · 2013 to 2015
$77k
NIDA NIH HHS F31 DA035073NIDA NIH HHS F32 DA036319NIDA NIH HHS P01 DA008227NIDA NIH HHS R01 DA003906NIDA NIH HHS R01 DA010460NIDA NIH HHS R01 DA027664NIDA NIH HHS R01 DA032708NIDA NIH HHS R29 DA010460NIDA NIH HHS R37 DA003906NIDA NIH HHS T32 DA007288NIMH NIH HHS R01 MH091220NINDS NIH HHS R01 NS085418
6 · The paper itself

Abstract

Individuals suffering from substance-use disorders develop strong associations between the drug's rewarding effects and environmental cues, creating powerful, enduring triggers for relapse. We found that dephosphorylated, nuclear histone deacetylase 5 (HDAC5) in the nucleus accumbens (NAc) reduced cocaine reward-context associations and relapse-like behaviors in a cocaine self-administration model. We also discovered that HDAC5 associates with an activity-sensitive enhancer of the Npas4 gene and negatively regulates NPAS4 expression. Exposure to cocaine and the test chamber induced rapid and transient NPAS4 expression in a small subpopulation of FOS-positive neurons in the NAc. Conditional deletion of Npas4 in the NAc significantly reduced cocaine conditioned place preference and delayed learning of the drug-reinforced action during cocaine self-administration, without affecting cue-induced reinstatement of drug seeking. These data suggest that HDAC5 and NPAS4 in the NAc are critically involved in reward-relevant learning and memory processes and that nuclear HDAC5 limits reinstatement of drug seeking independent of NPAS4.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCocaineConditioning, OperantConditioning, PsychologicalDose-Response Relationship, DrugDrug-Seeking BehaviorExtinction, PsychologicalFearGene Expression RegulationHistone DeacetylasesMaleMiceMice, KnockoutMice, TransgenicNucleus AccumbensBasic Helix-Loop-Helix ProteinsCocaineHdac5 protein, ratHistone DeacetylasesNpas4 protein, ratChIP-seqchromatin immunoprecipitationcocaine addictionconditioned place preferencedrug self-administrationHDAC5histone deacetylaseNPAS4nucleus accumbensreinstatement

Identifiers

PMID28957664
PMCPMC5761688
OpenAlexW2758568627

What OpenQuestion holds

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Registered trials

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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.