Evidence map›Paper›PMID 25979645›Full record

ArticleDrug and alcohol dependence2015

Clozapine reconstructed: Haloperidol's ability to reduce alcohol intake in the Syrian golden hamster can be enhanced through noradrenergic modulation by desipramine and idazoxan.

Jibran Y Khokhar, David T Chau, Ree Dawson, Alan I Green

Abstract read
In one paragraph

Article in Drug and alcohol dependence, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Unique Effects of Clozapine: A Pharmacological Perspective.Advances in pharmacology (San Diego, Calif.) · 2018
    Review
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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

4 authors at 2 institutions in 1 country.

Jibran Y KhokharDepartment of Psychiatry, Geisel School of Medicine at Dartmouth, Dartmouth College, Lebanon, NH, United States.
David T ChauDepartment of Psychiatry, Geisel School of Medicine at Dartmouth, Dartmouth College, Lebanon, NH, United States.
Ree DawsonFrontier Science Research and Technology Foundation, Boston, MA, United States.
Alan I GreenDepartment of Psychiatry, Geisel School of Medicine at Dartmouth, Dartmouth College, Lebanon, NH, United States; The Dartmouth Clinical and Translational Science Institute, Dartmouth College, Hanover, NH, United States. Electronic address: alan.i.green@dartmouth.edu.
Dartmouth College · USFrontier Science & Technology Research Foundation · US

Funding

SYNERGY: The Dartmouth Center for clinical and Translational ScienceUL1TR001086 · NCATS · DARTMOUTH COLLEGE · PI GREEN, ALAN I · 2013 to 2017
$18.3M
Deconstructing Clozapine: Toward Medication for Alcoholism in SchizophreniaR01AA018151 · NIAAA · DARTMOUTH COLLEGE · PI GREEN, ALAN I · 2010 to 2011
$700k
Antipsychotics and Alcohol Drinking in RodentsR03AA014644 · NIAAA · DARTMOUTH COLLEGE · PI GREEN, ALAN I · 2004 to 2005
$158k
NCATS NIH HHS UL1 TR001086NCATS NIH HHS UL1TR001086NIAAA NIH HHS 1R01AA018151NIAAA NIH HHS 1R03AA014644NIAAA NIH HHS R01 AA018151NIAAA NIH HHS R03 AA014644
6 · The paper itself

Abstract

backgroundAlcohol use disorder commonly occurs in patients with schizophrenia. Most antipsychotic drugs do not lessen alcohol use; although the atypical antipsychotic clozapine has been shown to reduce alcohol use in patients with schizophrenia, its toxicity severely limits its use in patients. With an eye toward creation of a safer clozapine-like drug, we have investigated the pharmacological basis of the clozapine's effects on alcohol drinking in the Syrian golden hamster. In this animal, as in patients with schizophrenia, clozapine reduces alcohol drinking while the typical antipsychotic haloperidol does not. We have suggested that clozapine decreases alcohol drinking due to its weak dopamine D2 receptor blockade, its potent norepinephrine α-2 receptor antagonism, as well as its ability to elevate plasma norepinephrine.

methodsWe recreated a clozapine-like drug to reduce alcohol drinking in the Syrian golden hamster by combining low dose haloperidol with a norepinephrine α-2 receptor antagonist, idazoxan, and a norepinephrine reuptake inhibitor, desipramine. Hamsters were given free access to water and alcohol (15% v/v) and were treated daily with each drug or with the three-drug combination for 23 days.

resultsThe drug combination reduced alcohol drinking and preference significantly as compared to vehicle or to haloperidol, idazoxan or desipramine, while not altering food-intake or body-weight.

conclusionThese findings suggest that that haloperidol, which does not reduce alcohol drinking in patients with schizophrenia or the hamster, if combined with idazoxan and desipramine (producing a drug combination that mimics aspects of clozapine's pharmacology) is able to reduce alcohol drinking in the hamster.

Indexed as

Adrenergic alpha-2 Receptor AntagonistsAdrenergic Uptake InhibitorsAdultAlcohol DrinkingAnimalsClozapineDesipramineDose-Response Relationship, DrugDrug SynergismEatingFemaleHaloperidolHumansIdazoxanMaleMesocricetusAdrenergic alpha-2 Receptor AntagonistsAdrenergic Uptake InhibitorsClozapineDesipramineHaloperidolIdazoxanReceptors, Dopamine D2AddictionAlcoholismAntipsychoticNorepinephrineSchizophrenia

Identifiers

PMID25979645
PMCPMC4458150
OpenAlexW2059657509

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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.