Evidence map›Paper›PMID 22781742›Full record

ReviewBiochemical pharmacology2012

Medication discovery for addiction: translating the dopamine D3 receptor hypothesis.

Amy Hauck Newman, Brandi L Blaylock, Michael A Nader, Jack Bergman, David R Sibley, Phil Skolnick

Open access · greenAbstract readReview
In one paragraph

Review in Biochemical pharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

76 citing papers in PubMed, 131 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Substance Addiction Rehabilitation Drugs.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. A highly DNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

16 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

Amy Hauck NewmanMedicinal Chemistry Section, Molecular Targets and Medications Discovery Branch, National Institute on Drug Abuse-Intramural Research Program, Baltimore, MD 21224, USA.
Brandi L Blaylock
Michael A Nader
Jack Bergman
David R Sibley
Phil Skolnick
Wake Forest University · USHarvard University · USNational Institute of Neurological Disorders and Stroke · USNational Institutes of Health · US

Funding

Molecular And Pharmacological Studies Of Dopamine ReceptorsZIANS002263 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI SIBLEY, DAVID · 2009 to 2025
$37.4M
Novel Dopamine D3 Receptor Ligands ZIADA000424 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI NEWMAN, AMY HAUCK · 2009 to 2025
$25.9M
DOPAMINE D2 RECEPTORS IN PRIMATE MODELS OF COCAINE ABUSER01DA012460 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI NADER, MICHAEL A · 2000 to 2012
$3.4M
Transition to Cocaine Abuse in Monkey:Role of DopamineR01DA014637 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI NADER, MICHAEL A · 2001 to 2005
$1.8M
Behavior, physiology, and neurobiology of chronic nicotine exposure in monkeyF31DA033106 · NIDA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BLAYLOCK, BRANDI L · 2012 to 2012
$29k
Intramural NIH HHS ZIA DA000424NIDA NIH HHS F31 DA033106NIDA NIH HHS R01 DA012460NIDA NIH HHS R01 DA014637NIDA NIH HHS R01 DA12460
6 · The paper itself

Abstract

The dopamine D3 receptor (D3R) has been investigated as a potential target for medication development to treat substance use disorders (SUDs) with a particular focus on cocaine and methamphetamine. Currently, there are no approved medications to treat cocaine and methamphetamine addiction and thus developing pharmacotherapeutics to complement existing behavioral strategies is a fundamental goal. Novel compounds with high affinity and D3R selectivity have been evaluated in numerous animal models of drug abuse and favorable outcomes in nonhuman primate models of self-administration and relapse have provided compelling evidence to advance these agents into the clinic. One approach is to repurpose drugs that share the D3R mechanism and already have clinical utility, and to this end buspirone has been identified as a viable candidate for clinical trials. A second, but substantially more resource intensive and risky approach involves the development of compounds that exclusively target D3R, such as GSK598809 and PG 619. Clinical investigation of these drugs or other novel D3R-selective agents will provide a better understanding of the role D3R plays in addiction and whether or not antagonists or partial agonists that are D3R selective are effective in achieving abstinence in this patient population.

Indexed as

AnimalsCocaineCocaine-Related DisordersDisease Models, AnimalDopamine AgonistsDopamine AntagonistsHumansMethamphetamineMolecular StructureReceptors, Dopamine D3Substance-Related DisordersCocaineDopamine AgonistsDopamine AntagonistsMethamphetamineReceptors, Dopamine D3

Identifiers

PMID22781742
PMCPMC3836213
OpenAlexW2090518397

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.