Evidence map›Paper›PMID 30043172›Full record

ArticlePsychopharmacology2018

Selective breeding for high alcohol consumption and response to nicotine: locomotor activity, dopaminergic in the mesolimbic system, and innate genetic differences in male and female alcohol-preferring, non-preferring, and replicate lines of high-alcohol drinking and low-alcohol drinking rats.

Gerald A Deehan, Sheketha R Hauser, Bruk Getachew, R Aaron Waeiss, Eric A Engleman, Christopher P Knight, William J McBride, William A Truitt, Richard L Bell, Zachary A Rodd

Abstract read
In one paragraph

Article in Psychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Gerald A DeehanDepartment of Psychology, East Tennessee State University, 420 Rogers Stout Hall, Johnson City, TN, 37614, USA. deehan@etsu.edu.ORCID http://orcid.org/0000-0002-9211-2610
Sheketha R HauserDepartment of Psychiatry and Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Bruk GetachewDepartment of Psychiatry and Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, Indiana, USA.
R Aaron WaeissDepartment of Psychiatry and Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Eric A EnglemanDepartment of Psychiatry and Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Christopher P KnightDepartment of Psychiatry and Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, Indiana, USA.
William J McBrideDepartment of Psychiatry and Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, Indiana, USA.
William A TruittDepartment of Psychiatry and Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Richard L BellDepartment of Psychiatry and Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Zachary A RoddDepartment of Psychiatry and Institute of Psychiatric Research, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Indiana University School of MedicineEast Tennessee State University · US

Funding

Translational Research and Science Education (OUT)P60AA007611 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI DAVID A. KAREKEN · 2003 to 2026
$45.5M
TRAINING GRANT ON GENETICS ASPECTS OF ALCOHOLISMT32AA007462 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI CRISTINE L CZACHOWSKI · 1985 to 2026
$10.7M
RAT RESEARCH COMPONENTP50AA007611 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI BOSRON, WILLIAM F · 1987 to 2002
$5.3M
CNS SITES FOR THE REWARDING ACTIONS OF ALCOHOLR01AA012262 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI MCBRIDE, WILLIAM J · 2000 to 2016
$4.3M
Ethanol and nicotine co-abuse: cross sensitization of their reinforcing actionsRC2AA019366 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI MCBRIDE, WILLIAM J · 2009 to 2010
$2.6M
Rat Animal Models & Drug and Gene Testing Core (RAM-DGTC)U24AA013522 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI BELL, RICHARD LOWELL · 2015 to 2021
$2.4M
7/8 NADIA UO1 Adolescent Alcohol and Neurocircuitry Mediating Ethanol ReinforcementU01AA024612 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI RODD, ZACHARY AARON · 2015 to 2019
$1.6M
Biological Basis of Conditioned Cues Effects on EtOH-SeekingR01AA020908 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI RODD, ZACHARY AARON · 2012 to 2016
$1.5M
NIAAA NIH HHS P50 AA007611NIAAA NIH HHS P60 AA007611NIAAA NIH HHS R01 AA012262NIAAA NIH HHS R01 AA020908NIAAA NIH HHS RC2 AA019366NIAAA NIH HHS T32 AA007462NIAAA NIH HHS U01 AA024612NIAAA NIH HHS U24 AA013522
6 · The paper itself

Abstract

rationaleThere is evidence for a common genetic link between alcohol and nicotine dependence. Rodents selectively bred for high alcohol consumption/responsivity are also more likely to self-administer nicotine than controls.

objectivesThe experiments examined the response to systemic nicotine, the effects of nicotine within the drug reward pathway, and innate expression of nicotine-related genes in a brain region regulating drug reward/self-administration in multiple lines of rats selectively bred for high and low alcohol consumption.

methodsThe experiments examined the effects of systemic administration of nicotine on locomotor activity, the effects of nicotine administered directly into the (posterior ventral tegmental area; pVTA) on dopamine (DA) release in the nucleus accumbens shell (AcbSh), and innate mRNA levels of acetylcholine receptor genes in the pVTA were determined in 6 selectively bred high/low alcohol consuming and Wistar rat lines.

resultsThe high alcohol-consuming rat lines had greater nicotine-induced locomotor activity compared to low alcohol-consuming rat lines. Microinjections of nicotine into the pVTA resulted in DA release in the AcbSh with the dose response curves for high alcohol-consuming rats shifted leftward and upward. Genetic analysis of the pVTA indicated P rats expressed higher levels of α2 and β4.

conclusionSelective breeding for high alcohol preference resulted in a genetically divergent behavioral and neurobiological sensitivity to nicotine. The observed behavioral and neurochemical differences between the rat lines would predict an increased likelihood of nicotine reinforcement. The data support the hypothesis of a common genetic basis for drug addiction and identifies potential receptor targets.

Indexed as

Alcohol DrinkingAnimalsDopamineEthanolFemaleLocomotionMaleNicotineNucleus AccumbensRatsRats, WistarReinforcement, PsychologySelective BreedingSelf AdministrationTobacco Use DisorderVentral Tegmental AreaDopamineEthanolNicotineAlcohol-preferring P ratsDopamineHigh-alcohol-drinking HAD ratsLocomotor activityNicotineNucleus accumbensVentral tegmental area

Identifiers

PMID30043172
PMCPMC6655552
OpenAlexW2883173235

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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.