Evidence map›Paper›PMID 26260061›Full record

ArticleAlcoholism, clinical and experimental research2015

Prazosin + Naltrexone Decreases Alcohol Drinking More Effectively Than Does Either Drug Alone in P Rats with a Protracted History of Extensive Voluntary Alcohol Drinking, Dependence, and Multiple Withdrawals.

Dennis D Rasmussen, Carrie L Kincaid, Janice C Froehlich

Open access · greenAbstract 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Prazosin in the Pharmacologic Management of Alcohol Use Disorder.Biological psychiatry global open science · 2026
    Article
  3. Neurogenetics and Epigenetics of Loneliness.Psychology research and behavior management · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
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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

3 authors at 3 institutions in 1 country.

Dennis D RasmussenVISN 20 Mental Illness Research, Education and Clinical Center, Seattle, Washington.
Carrie L KincaidVA Puget Sound Health Care System, Seattle, Washington.
Janice C FroehlichDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
Indiana University – Purdue University Indianapolis · USUniversity of Washington · USVA Northwest Network · US

Funding

Translational Research and Science Education (OUT)P60AA007611 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Marian Lee Logrip · 2003 to 2026
$45.5M
Rodents with Genetic Differences in Alcohol PreferenceR24AA015512 · NIAAA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI BELL, RICHARD LOWELL · 2005 to 2014
$5.1M
Rodents with Genetic Differences in Alcohol PreferenceU24AA015512 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI BELL, RICHARD LOWELL · 2015 to 2019
$2.7M
Noradrenergic Agents As Potential New Pharmacotherapies for Alcohol DrinkingR01AA018604 · NIAAA · SEATTLE INST FOR BIOMEDICAL/CLINICAL RES · PI FROEHLICH, JANICE C, RASMUSSEN, DENNIS D · 2010 to 2014
$1.6M
Center for Neuroregulation in Alcohol Dependence (CeNiAD)P20AA017839 · NIAAA · SEATTLE INST FOR BIOMEDICAL/CLINICAL RES · PI SAXON, ANDREW J · 2009 to 2010
$984k
NIAAA NIH HHS P20 AA017839NIAAA NIH HHS P60 AA007611NIAAA NIH HHS R01 AA018604NIAAA NIH HHS R24 AA015512NIAAA NIH HHS U24 AA015512
6 · The paper itself

Abstract

backgroundPrazosin (PRZ; an α1 -adrenergic receptor antagonist) and naltrexone (NTX; a nonspecific opioid receptor antagonist) each decrease alcohol drinking when administered to rats selectively bred for high voluntary alcohol drinking (alcohol-preferring or "P"), and the combination of PRZ + NTX decreases alcohol drinking more effectively than does either drug alone. As drug responsiveness can depend on history of alcohol drinking and dependence, we investigated whether various schedules of PRZ and NTX administration, alone or in combination, are effective in decreasing alcohol drinking in male P rats with a history of protracted voluntary alcohol drinking, dependence, and repeated withdrawals closely resembling human alcoholism.

methodsMale P rats became alcohol-dependent during 1 year of ad libitum 24 h/d access to food, water, and 20% alcohol with repetitive temporary alcohol withdrawals. Four sequential studies then addressed effects of oral PRZ (2 mg/kg) and NTX (10 mg/kg), alone or together, on alcohol drinking during: (i) daily alcohol access with daily drug treatment, (ii) intermittent alcohol access with daily drug treatment, (iii) intermittent alcohol access with occasional drug treatment, and (iv) postdeprivation reinstatement of alcohol access.

resultsThe combination of PRZ + NTX consistently suppressed alcohol drinking during daily or intermittent alcohol access conditions and when drug treatment was either daily or occasional. PRZ + NTX was consistently more effective than either drug alone. The reduction in alcohol drinking was not due to sedation, motor effects, or malaise.

conclusionsBoth daily and "as-needed" treatment with PRZ + NTX are highly effective in suppressing daily, intermittent, and postdeprivation alcohol drinking in male P rats with a protracted history of alcohol dependence and repeated withdrawals. This drug combination may be especially effective for treating individuals with long histories of heavy alcohol abuse, dependence, and repeated relapse, as commonly encountered in clinical practice.

Indexed as

Adrenergic alpha-1 Receptor AntagonistsAlcohol DrinkingAlcoholismAnimalsDrug Therapy, CombinationMaleNaltrexoneNarcotic AntagonistsPrazosinRatsSubstance Withdrawal SyndromeTreatment OutcomeAdrenergic alpha-1 Receptor AntagonistsNaltrexoneNarcotic AntagonistsPrazosinAlcoholAlcoholism TreatmentNaltrexoneNoradrenergicOpioidPrazosin

Identifiers

PMID26260061
PMCPMC4558320
OpenAlexW1944091438

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.