Evidence map›Paper›PMID 24432188›Full record

ArticleOA alcohol2013

Novel anticonvulsants for reducing alcohol consumption: A review of evidence from preclinical rodent drinking models.

A E Padula, N S McGuier, W C Griffin, M F Lopez, H C Becker, P J Mulholland

Open access · hybridAbstract read
In one paragraph

Article in OA alcohol, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. KCNN Genes that Encode Small-Conductance Ca2+-Activated K+ Channels Influence Alcohol and Drug Addiction.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2015
    Article
  8. Review
  9. 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

6 authors at 1 institution in 1 country.

A E Padula *Department of Neurosciences, Charleston Alcohol Research Center Medical University of South Carolina Charleston, SC 29425, USA.
N S McGuier *Department of Neurosciences, Charleston Alcohol Research Center Medical University of South Carolina Charleston, SC 29425, USA.
W C GriffinDepartment of Psychiatry and Behavioral Sciences,, Charleston Alcohol Research Center Medical University of South Carolina Charleston, SC 29425, USA.
M F LopezDepartment of Psychiatry and Behavioral Sciences,, Charleston Alcohol Research Center Medical University of South Carolina Charleston, SC 29425, USA.
H C BeckerDepartment of Psychiatry and Behavioral Sciences,, Charleston Alcohol Research Center Medical University of South Carolina Charleston, SC 29425, USA.
P J MulhollandDepartment of Neurosciences, Charleston Alcohol Research Center Medical University of South Carolina Charleston, SC 29425, USA.
Medical University of South Carolina · US

Funding

Stress and Ethanol Dependence: SK Channels and GlutamateU01AA020930 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MULHOLLAND, PATRICK J. · 2012 to 2021
$2.6M
Mouse Chronic Intermittent Ethanol (CIE) CoreU01AA020929 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LOPEZ, MARCELO F. · 2012 to 2015
$1.5M
Chronic Ethanol and SK2 Potassium ChannelsR00AA017922 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MULHOLLAND, PATRICK J. · 2010 to 2012
$586k
Homer2 and Chronic Ethanol-Associated NeuroadaptationsF31AA021618 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI STRAIGHT, NATALIE M. · 2012 to 2014
$125k
NIAAA NIH HHS F31 AA021618NIAAA NIH HHS R00 AA017922NIAAA NIH HHS U01 AA020929NIAAA NIH HHS U01 AA020930
6 · The paper itself

Abstract

Alcohol use disorders (AUDs) are a major public health issue and have an enormous social and economic burden in developed, developing, and third-world countries. Current pharmacotherapies for treating AUDs suffer from deleterious side effects and are only effective in preventing relapse in a subset of individuals. This signifies an essential need for improved medications to reduce heavy episodic drinking and alcohol-related problems. Growing literature has provided support for the use of anticonvulsants in suppressing symptoms induced by alcohol withdrawal. Emerging clinical and preclinical evidence suggests that a number of well-tolerated anticonvulsants may also decrease alcohol drinking. This review will focus on recent evidence supporting the efficacy of novel anticonvulsants in reducing voluntary alcohol consumption in rodent models. The data demonstrate that anticonvulsants reduce drinking in standard home cage two-bottle choice paradigms, self-administration of alcohol in operant chambers, and cue- and stress-induced reinstatement of alcohol seeking behaviors in rats and mice. This review also highlights evidence that some anticonvulsants were only moderately effective in reducing drinking in select strains of rodents or models. This suggests that genetics, possible neuroadaptations, or the pharmacological target affect the ability of anticonvulsants to attenuate alcohol consumption. Nonetheless, anticonvulsants are relatively safe, have little abuse potential, and can work in combination with other drugs. The results from these preclinical and clinical studies provide compelling evidence that anticonvulsants are a promising class of medication for the treatment of AUDs.

Indexed as

alcoholanticonvulsantsconsumptionnovel pharmacotherapyrodent models

Identifiers

PMID24432188
PMCPMC3890354
OpenAlexW2051715579

What OpenQuestion holds

Textmetadata
LicenceTDM
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.