Evidence map›Paper›PMID 28847378›Full record

ArticleAlcohol (Fayetteville, N.Y.)2017

Persistent negative effects of alcohol drinking on aspects of novelty-directed behavior in male rhesus macaques.

Cassie M Chandler, Meagan E Follett, Nicholas J Porter, Kevin Y Liang, Eric J Vallender, Gregory M Miller, James K Rowlett, Donna M Platt

Abstract read
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2017. 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
–field-weighted citation impact
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.

  1. Article
  2. GABAergic compounds for the treatment of alcohol use disorder.International review of neurobiology · 2024
    Review
  3. Article
  4. Review
  5. Review
  6. Behavioral Flexibility in Alcohol-Drinking Monkeys: The Morning After.Alcoholism, clinical and experimental research · 2020
    Article
  7. Article
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

8 authors.

Cassie M ChandlerGraduate Program in Neuroscience, University of Mississippi Medical Center, Jackson, MS 39216, USA.
Meagan E FollettDepartment of Psychiatry & Human Behavior, University of Mississippi Medical Center, Jackson, MS 39216, USA.
Nicholas J PorterHarvard Medical School/NEPRC, Southborough, MA 01772, USA.
Kevin Y LiangHarvard Medical School/NEPRC, Southborough, MA 01772, USA.
Eric J VallenderGraduate Program in Neuroscience, University of Mississippi Medical Center, Jackson, MS 39216, USA; Department of Psychiatry & Human Behavior, University of Mississippi Medical Center, Jackson, MS 39216, USA; Harvard Medical School/NEPRC, Southborough, MA 01772, USA.
Gregory M MillerHarvard Medical School/NEPRC, Southborough, MA 01772, USA; Department of Pharmaceutical Sciences, Northeastern University, Boston, MA 02115, USA; Department of Chemical Engineering, Northeastern University, Boston, MA 02115, USA.
James K RowlettGraduate Program in Neuroscience, University of Mississippi Medical Center, Jackson, MS 39216, USA; Department of Psychiatry & Human Behavior, University of Mississippi Medical Center, Jackson, MS 39216, USA; Department of Neurobiology & Anatomical Sciences, University of Mississippi Medical Center, Jackson, MS 39216, USA; Harvard Medical School/NEPRC, Southborough, MA 01772, USA.
Donna M PlattGraduate Program in Neuroscience, University of Mississippi Medical Center, Jackson, MS 39216, USA; Department of Psychiatry & Human Behavior, University of Mississippi Medical Center, Jackson, MS 39216, USA; Department of Neurobiology & Anatomical Sciences, University of Mississippi Medical Center, Jackson, MS 39216, USA; Harvard Medical School/NEPRC, Southborough, MA 01772, USA. Electronic address: dplatt@umc.edu.

Funding

New England Primate Research Center Base GrantP51OD011103 · OD · HARVARD MEDICAL SCHOOL · PI FLIER, JEFFREY S · 2012 to 2013
$24.7M
ANXIOLYTIC EFFECTS AND ABUSE OF BZ RECEPTOR LIGANDSR01DA011792 · NIDA · UNIVERSITY OF MISSISSIPPI MED CTR · PI ROWLETT, JAMES K · 1998 to 2024
$7.8M
GABAa receptor subtype mechanisms in nonhuman primatesR01AA016179 · NIAAA · UNIVERSITY OF MISSISSIPPI MED CTR · PI PLATT, DONNA M · 2006 to 2016
$3.2M
Opioid Receptor Polymorphisms and Nonhuman Primate Models of Alcohol AbuseR01AA016828 · NIAAA · UNIVERSITY OF MISSISSIPPI MED CTR · PI PLATT, DONNA M · 2009 to 2013
$1.9M
NIAAA NIH HHS R01 AA016179NIAAA NIH HHS R01 AA016828NIDA NIH HHS R01 DA011792NIH HHS P51 OD011103
6 · The paper itself

Abstract

Humans with histories of prolonged heavy alcohol use exhibit poorer performance on cognitive tasks associated with problem solving, short-term memory, and visuospatial reasoning, even following the cessation of drinking, when compared with healthy controls. It is unclear, however, whether the cognitive problems are a consequence of alcohol exposure or a contributing factor to alcohol-use disorders. Here, we examined the relationship between performance on a novel object recognition (NOR) task and total alcohol consumption (TAC) in adult male rhesus macaques (n = 12; ETH group; trained to self-administer alcohol). NOR performance in this group was assessed prior to induction of alcohol drinking ("pre") and, again, after a 1-year abstinence period ("post") and was compared to the performance of a second group (n = 6; Control group), which was alcohol-naïve. In the NOR task, difficulty was manipulated across three phases by varying specific object features and/or by varying duration of access to objects. For each monkey, we measured aspects of novelty-related behavior including novelty detection, novelty reactivity, and perseverative behavior. TAC during induction and a "free" access period in which the monkey could choose between water and a 4% w/v ethanol solution also was determined. We found that performance deficits in the NOR task were a consequence of high total alcohol intake instead of a predictor of subsequent high intake. Poor NOR performance in drinkers with the highest intakes was characterized by increased perseverative behavior rather than an inability to detect or react to novelty. Finally, the observed deficits are long-lasting - persisting even after a year of abstinence. Given the prevalent and persistent nature of alcohol-induced cognitive deficits in patients in treatment settings, understanding the nature of the deficit and its neural basis could ultimately offer novel treatment approaches based on the reversal of alcohol-induced impairment.

Indexed as

Alcohol DrinkingAnimalsEthanolExploratory BehaviorMacaca mulattaMalePsychomotor PerformanceSelf AdministrationEthanolAlcohol-use disorderCognitive deficitNovelty taskRhesus macaqueSelf-administration

Identifiers

PMID28847378
PMCPMC5584881

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.