Evidence map›Paper›PMID 22827916›Full record

ArticleThe international journal of neuropsychopharmacology2013

Modification of cocaine self-administration by buspirone (buspar®): potential involvement of D3 and D4 dopamine receptors.

Jack Bergman, Rebecca A Roof, Cheryse A Furman, Jennie L Conroy, Nancy K Mello, David R Sibley, Phil Skolnick

Open access · bronzeAbstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
5.0field-weighted citation impact, top 3% 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

53 citing papers in PubMed, 99 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Substance Addiction Rehabilitation Drugs.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  6. Article
  7. The selective 5-HTNaunyn-Schmiedeberg's archives of pharmacology · 2022
    Article
  8. Article
  9. Review
  10. The effect of 5-HTBritish journal of pharmacology · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Occupancy of dopamine DNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    Article
  18. Dopamine DJournal of medicinal chemistry · 2019
    Article
  19. Article
  20. 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

7 authors at 4 institutions in 1 country.

Jack BergmanHarvard Medical School-McLean Hospital, Alcohol and Drug Abuse Research Center, Belmont, MA, USA. jbergman@hms.harvard.edu
Rebecca A Roof
Cheryse A Furman
Jennie L Conroy
Nancy K Mello
David R Sibley
Phil Skolnick
National Institute of Neurological Disorders and Stroke · USNational Institutes of Health · USHarvard University · USMcLean Hospital · 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
Molecular &Pharmacological Studies Of Dopamine ReceptorZ01NS002263 · NINDS · NEUROLOGICAL DISORDERS AND STROKE · PI SIBLEY, DAVID R. · 1985 to 2008
$3.1M
Intramural NIH HHS Z01 NS002263
6 · The paper itself

Abstract

Converging lines of evidence indicate that elevations in synaptic dopamine levels play a pivotal role in the reinforcing effects of cocaine, which are associated with its abuse liability. This evidence has led to the exploration of dopamine receptor blockers as pharmacotherapy for cocaine addiction. While neither D1 nor D2 receptor antagonists have proven effective, medications acting at two other potential targets, D3 and D4 receptors, have yet to be explored for this indication in the clinic. Buspirone, a 5-HT1A partial agonist approved for the treatment of anxiety, has been reported to also bind with high affinity to D3 and D4 receptors. In view of this biochemical profile, the present research was conducted to examine both the functional effects of buspirone on these receptors and, in non-human primates, its ability to modify the reinforcing effects of i.v. cocaine in a behaviourally selective manner. Radioligand binding studies confirmed that buspirone binds with high affinity to recombinant human D3 and D4 receptors (∼98 and ∼29 nm respectively). Live cell functional assays also revealed that buspirone, and its metabolites, function as antagonists at both D3 and D4 receptors. In behavioural studies, doses of buspirone that had inconsistent effects on food-maintained responding (0.1 or 0.3 mg/kg i.m.) produced a marked downward shift in the dose-effect function for cocaine-maintained behaviour, reflecting substantial decreases in self-administration of one or more unit doses of i.v. cocaine in each subject. These results support the further evaluation of buspirone as a candidate medication for the management of cocaine addiction.

Indexed as

Analysis of VarianceAnimalsBuspironeCocaineDopamineDopamine AgentsDose-Response Relationship, DrugDrug InteractionsG Protein-Coupled Inwardly-Rectifying Potassium ChannelsHEK293 CellsHumansMacaca mulattaMaleProtein BindingReceptors, Dopamine D3Receptors, Dopamine D4BuspironeCocaineDopamineDopamine AgentsG Protein-Coupled Inwardly-Rectifying Potassium ChannelsReceptors, Dopamine D3Receptors, Dopamine D4SerotoninSerotonin Receptor AgonistsTritium

Identifiers

PMID22827916
PMCPMC5100812
OpenAlexW2139475986

What OpenQuestion holds

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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.