Evidence map›Paper›PMID 25878294›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Chronic nicotine activates stress/reward-related brain regions and facilitates the transition to compulsive alcohol drinking.

Rodrigo M Leão, Fábio C Cruz, Leandro F Vendruscolo, Giordano de Guglielmo, Marian L Logrip, Cleopatra S Planeta, Bruce T Hope, George F Koob, Olivier George

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 78 citations in OpenAlex.

  1. A Phase 2, Double-Blind, Placebo-Controlled Randomized Trial Assessing the Efficacy of ABT-436, a Novel V1b Receptor Antagonist, for Alcohol Dependence.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    Trial
  2. Review
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  5. Cannabidiol mitigates alcohol dependence and withdrawal with neuroprotective effects in the basolateral amygdala and striatum.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Rodrigo M LeãoLaboratory of Pharmacology, Department of Natural Active Principles and Toxicology, School of Pharmaceutical Sciences, Universidade Estadual Paulista - UNESP, Araraquara, Sao Paulo 14801-902, Brazil, Committee on the Neurobiology of Addictive Disorders, The Scripps Research Institute, La Jolla, California 92037, and Behavioral Neuroscience Branch, IRP/NIDA/NIH/DHHS, Baltimore, Maryland 21224 ogeorge@scripps.edu rodrigomolini@yahoo.com.br.
Fábio C CruzBehavioral Neuroscience Branch, IRP/NIDA/NIH/DHHS, Baltimore, Maryland 21224.
Leandro F VendruscoloCommittee on the Neurobiology of Addictive Disorders, The Scripps Research Institute, La Jolla, California 92037, and Behavioral Neuroscience Branch, IRP/NIDA/NIH/DHHS, Baltimore, Maryland 21224.ORCID http://orcid.org/0000-0002-8829-8627
Giordano de GuglielmoCommittee on the Neurobiology of Addictive Disorders, The Scripps Research Institute, La Jolla, California 92037, and.
Marian L LogripCommittee on the Neurobiology of Addictive Disorders, The Scripps Research Institute, La Jolla, California 92037, and.
Cleopatra S PlanetaLaboratory of Pharmacology, Department of Natural Active Principles and Toxicology, School of Pharmaceutical Sciences, Universidade Estadual Paulista - UNESP, Araraquara, Sao Paulo 14801-902, Brazil.
Bruce T HopeBehavioral Neuroscience Branch, IRP/NIDA/NIH/DHHS, Baltimore, Maryland 21224.
George F KoobCommittee on the Neurobiology of Addictive Disorders, The Scripps Research Institute, La Jolla, California 92037, and.
Olivier GeorgeCommittee on the Neurobiology of Addictive Disorders, The Scripps Research Institute, La Jolla, California 92037, and ogeorge@scripps.edu rodrigomolini@yahoo.com.br.ORCID http://orcid.org/0000-0002-3700-5003
Scripps Research Institute · USUnited States Department of Health and Human Services · USUniversidade Estadual Paulista (Unesp) · BR

Funding

Viral Vector CoreP60AA006420 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI MARISA ROBERTO · 2003 to 2026
$46.3M
Characterization of neuronal ensembles activated during drug-induced behaviorZIADA000467 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI HOPE, BRUCE · 2009 to 2025
$35.8M
SYSTEMIC NEUROPHARMACOLOGYP50AA006420 · NIAAA · SCRIPPS RESEARCH INSTITUTE · PI HENRIKSEN, STEVEN J · 1985 to 2002
$5.1M
Alcohol Vapor Self-Administration in RatsR01AA022977 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Olivier George · 2014 to 2026
$5.1M
NEUROPHARMACOLOGY OF ETHANOL REINFORCEMENTR01AA008459 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI GEORGE, OLIVIER · 1990 to 2013
$4.2M
Central mechanisms of nicotine reinforcement and dependenceR01DA023597 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI KOOB, GEORGE F. · 2008 to 2012
$1.9M
The Role of Brain Stress Systems in the Prefrontal Cortex in Compulsive DrinkingR01AA020608 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI GEORGE, OLIVIER · 2011 to 2015
$1.8M
NEUROPHARMACOLOGY OF ETHANOL REINFORCEMENTR37AA008459 · NIAAA · SCRIPPS RESEARCH INSTITUTE · PI KOOB, GEORGE F · 1993 to 2002
$788k
Stress history enhances ethanol self-administration: role of neuronal pentraxin 2F32AA018914 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI LOGRIP, MARIAN LEE · 2009 to 2011
$151k
NIAAA NIH HHS AA006420NIAAA NIH HHS AA008459NIAAA NIH HHS AA018914NIAAA NIH HHS AA020608NIAAA NIH HHS AA022977NIAAA NIH HHS F32 AA018914NIAAA NIH HHS P50 AA006420NIAAA NIH HHS P60 AA006420NIAAA NIH HHS R01 AA008459NIAAA NIH HHS R01 AA020608NIAAA NIH HHS R01 AA022977NIAAA NIH HHS R37 AA008459NIDA NIH HHS DA023597NIDA NIH HHS R01 DA023597
6 · The paper itself

Abstract

Alcohol and nicotine are the two most co-abused drugs in the world. Previous studies have shown that nicotine can increase alcohol drinking in nondependent rats, yet it is unknown whether nicotine facilitates the transition to alcohol dependence. We tested the hypothesis that chronic nicotine will speed up the escalation of alcohol drinking in rats and that this effect will be accompanied by activation of sparsely distributed neurons (neuronal ensembles) throughout the brain that are specifically recruited by the combination of nicotine and alcohol. Rats were trained to respond for alcohol and made dependent using chronic, intermittent exposure to alcohol vapor, while receiving daily nicotine (0.8 mg/kg) injections. Identification of neuronal ensembles was performed after the last operant session, using immunohistochemistry. Nicotine produced an early escalation of alcohol drinking associated with compulsive alcohol drinking in dependent, but not in nondependent rats (air exposed), as measured by increased progressive-ratio responding and increased responding despite adverse consequences. The combination of nicotine and alcohol produced the recruitment of discrete and phenotype-specific neuronal ensembles (∼4-13% of total neuronal population) in the nucleus accumbens core, dorsomedial prefrontal cortex, central nucleus of the amygdala, bed nucleus of stria terminalis, and posterior ventral tegmental area. Blockade of nicotinic receptors using mecamylamine (1 mg/kg) prevented both the behavioral and neuronal effects of nicotine in dependent rats. These results demonstrate that nicotine and activation of nicotinic receptors are critical factors in the development of alcohol dependence through the dysregulation of a set of interconnected neuronal ensembles throughout the brain.

Indexed as

RewardAlcohol DrinkingAnimalsBrainCalcium-Calmodulin-Dependent Protein Kinase Type 2Central Nervous System DepressantsCompulsive BehaviorConditioning, OperantDisease Models, AnimalEthanolGlutamate DecarboxylaseMaleNicotineNicotinic AgonistsPhosphopyruvate HydrataseProto-Oncogene Proteins c-fosCalcium-Calmodulin-Dependent Protein Kinase Type 2Central Nervous System DepressantsEthanolGlutamate Decarboxylaseglutamate decarboxylase 1NicotineNicotinic AgonistsPhosphopyruvate HydrataseProto-Oncogene Proteins c-fosQuinineaddictionalcoholcompulsivityFosneuronal ensemblestobacco

Identifiers

PMID25878294
PMCPMC4397613
OpenAlexW2020623859

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.