Evidence map›Paper›PMID 25833027›Full record

ArticleAlcoholism, clinical and experimental research2015

The effects of chronic alcohol self-administration in nonhuman primate brain networks.

Qawi K Telesford, Paul J Laurienti, April T Davenport, David P Friedman, Robert A Kraft, James B Daunais

Abstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

7 citing papers in PubMed, 13 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

6 authors at 2 institutions in 1 country.

Qawi K TelesfordSchool of Biomedical Engineering and Sciences, Virginia Tech-Wake Forest University, Winston-Salem, North Carolina.
Paul J Laurienti
April T Davenport
David P Friedman
Robert A Kraft
James B Daunais
Wake Forest University · USVirginia Tech - Wake Forest University School of Biomedical Engineering & Sciences · US

Funding

Monkey Alcohol Tissue Research Resource (MATRR)R24AA019431 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Mary Lauren Benton, Verginia Carmella Cuzon Carlson · 2010 to 2026
$10.3M
Early Stress & Alcoholism: Neurobiological AnalysisU01AA014106 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FRIEDMAN, DAVID P · 2003 to 2011
$3.4M
MRS Interrogation of Alcohol's Neurobiochemical EffectsR03AA017710 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI DAUNAIS, JAMES B · 2009 to 2010
$147k
Network Theory Analysis of Ethanol Self Administering Non-Human PrimatesF31AA019893 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI TELESFORD, QAWI KEVIN · 2011 to 2013
$120k
NIAAA NIH HHS AA014106NIAAA NIH HHS AA017710NIAAA NIH HHS AA019431NIAAA NIH HHS AA019893NIAAA NIH HHS F31 AA019893NIAAA NIH HHS R03 AA017710NIAAA NIH HHS R24 AA019431NIAAA NIH HHS U01 AA014106
6 · The paper itself

Abstract

backgroundLong-term alcohol abuse is associated with change in behavior, brain structure, and brain function. However, the nature of these changes is not well understood. In this study, we used network science to analyze a nonhuman primate model of ethanol self-administration to evaluate functional differences between animals with chronic alcohol use and animals with no exposure to alcohol. Of particular interest was how chronic alcohol exposure may affect the resting state network.

methodsBaseline resting state functional magnetic resonance imaging was acquired in a cohort of vervet monkeys. Animals underwent an induction period where they were exposed to an isocaloric maltose dextrin solution (control) or ethanol in escalating doses over three 30-day epochs. Following induction, animals were given ad libitum access to water and a maltose dextrin solution (control) or water and ethanol for 22 h/d over 12 months. Cross-sectional analyses examined region of interests in hubs and community structure across animals to determine differences between drinking and nondrinking animals after the 12-month free access period.

resultsAnimals were classified as lighter (<2.0 g/kg/d) or heavier drinkers (≥2.0 g/kg/d) based on a median split of their intake pattern during the 12-month ethanol free access period. Statistical analysis of hub connectivity showed significant differences in heavier drinkers for hubs in the precuneus, posterior parietal cortices, superior temporal gyrus, subgenual cingulate, and sensorimotor cortex. Heavier drinkers were also shown to have less consistent communities across the brain compared to lighter drinkers. The different level of consumption between the lighter and heavier drinking monkeys suggests that differences in connectivity may be intake dependent.

conclusionsAnimals that consume alcohol show topological differences in brain network organization, particularly in animals that drink heavily. Differences in the resting state network were linked to areas that are associated with spatial association, working memory, and visuomotor processing.

Indexed as

Alcohol DrinkingAnimalsBrainChlorocebus aethiopsEthanolFunctional NeuroimagingMagnetic Resonance ImagingMaleNeural PathwaysSelf AdministrationEthanolBrain NetworksFunctional Magnetic Resonance ImagingNetwork ScienceNonhuman Primates

Identifiers

PMID25833027
PMCPMC6724209
OpenAlexW2114300332

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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.