Evidence map›Paper›PMID 24722355›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2014

Activation of the trace amine-associated receptor 1 prevents relapse to cocaine seeking.

Yui Pei, Jungah Lee, Damiana Leo, Raul R Gainetdinov, Marius C Hoener, Juan J Canales

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.8field-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

40 citing papers in PubMed, 86 citations in OpenAlex.

  1. Preclinical development of [European journal of nuclear medicine and molecular imaging · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Trace amine-associated receptor 1 and drug abuse.Advances in pharmacology (San Diego, Calif.) · 2022
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. TAAR1 and Psychostimulant Addiction.Cellular and molecular neurobiology · 2020
    Review
  17. TAAR Agonists.Cellular and molecular neurobiology · 2020
    Review
  18. Role of trace amine-associated receptor 1 in nicotine's behavioral and neurochemical effects.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
  19. Article
  20. Review
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 3 institutions in 3 countries.

Yui PeiBehavioural Neuroscience, Department of Psychology, University of Canterbury, Christchurch, New Zealand.
Jungah LeeBehavioural Neuroscience, Department of Psychology, University of Canterbury, Christchurch, New Zealand.
Damiana LeoDepartment of Neuroscience and Brain Technologies, Italian Institute of Technology, Genoa, Italy.
Raul R Gainetdinov1] Department of Neuroscience and Brain Technologies, Italian Institute of Technology, Genoa, Italy [2] Skolkovo Institute of Science and Technology, Skolkovo, Russia [3] Faculty of Biology and Soil Science, St Petersburg State University, St Petersburg, Russia.
Marius C HoenerNeuroscience Research, Pharmaceuticals Division, F Hoffmann-La Roche, Basel, Switzerland.
Juan J CanalesBehavioural Neuroscience, Department of Psychology, University of Canterbury, Christchurch, New Zealand.
University of Canterbury · NZItalian Institute of Technology · ITRoche (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The trace amine-associated receptor 1 (TAAR1) has emerged as a promising target for medication development in addiction because of its ability to regulate dopamine (DA) transmission. We tested in rats the efficacy of RO5203648 and RO5256390, partial and full TAAR1 agonists, respectively, in models of cocaine relapse. Using a model of context-induced relapse, both RO5203648 and RO5256390 dose-dependently suppressed cocaine seeking after a 2-week period of withdrawal from chronic cocaine self-administration. In a model of extinction-reinstatement, RO5203648 completely inhibited cocaine-primed reinstatement of cocaine seeking. At doses that effectively suppressed cocaine seeking neither RO5203648 nor RO5256390 altered responding maintained by a natural reward. Moreover, fast scan cyclic voltammetry data showed that RO5203648 prevented cocaine-induced DA overflow in the nucleus accumbens without altering DA half-life, suggesting that the partial TAAR1 agonist attenuated cocaine-stimulated DA overflow by mechanisms other than direct interference with DA uptake. Collectively, these data provide strong evidence in support of TAAR1 as a neuropharmacological target for the treatment of cocaine addiction.

Indexed as

AnimalsCentral Nervous System AgentsChronic DiseaseCocaineCocaine-Related DisordersDopamineDopamine Uptake InhibitorsDose-Response Relationship, DrugDrug-Seeking BehaviorExtinction, PsychologicalMaleNucleus AccumbensOxazolesRandom AllocationRatsRats, Long-Evans4-(3,4-dichlorophenyl)-4,5-dihydrooxazol-2-ylamineCentral Nervous System AgentsCocaineDopamineDopamine Uptake InhibitorsOxazolesReceptors, G-Protein-CoupledTrace Amine-Associated Receptors

Identifiers

PMID24722355
PMCPMC4138750
OpenAlexW2037699379

What OpenQuestion holds

Textmetadata
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.