Evidence map›Paper›PMID 16856172›Full record

ArticleSynapse (New York, N.Y.)2006

Dose-response analysis of locomotor activity and stereotypy in dopamine D3 receptor mutant mice following acute amphetamine.

Robert K McNamara, Aaron Logue, Kevin Stanford, Ming Xu, Jianhua Zhang, Neil M Richtand

Open access · bronzeAbstract read
In one paragraph

Article in Synapse (New York, N.Y.), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.3field-weighted citation impact, top 25% 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

25 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  5. Selective DNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
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  14. Review
  15. A Methionine-Induced Animal Model of Schizophrenia: Face and Predictive Validity.The international journal of neuropsychopharmacology · 2015
    Article
  16. Article
  17. Cocaine self-administration in dopamine D₃ receptor knockout mice.Experimental and clinical psychopharmacology · 2012
    Article
  18. Reduced levels of serotonin 2A receptors underlie resistance of Egr3-deficient mice to locomotor suppression by clozapine.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2012
    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

6 authors at 2 institutions in 1 country.

Robert K McNamaraDepartment of Psychiatry, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267, USA. robert.mcnamara@psychiatry.uc.edu
Aaron Logue
Kevin Stanford
Ming Xu
Jianhua Zhang
Neil M Richtand
University of Cincinnati · USUniversity of Cincinnati Medical Center · US

Funding

Molecular Determinants of Compulsive Cocaine-TakingR01DA014644 · NIDA · UNIVERSITY OF CINCINNATI · PI XU, MING · 2001 to 2006
$1.9M
Role of c-fos in cocaine actionsR01DA017323 · NIDA · UNIVERSITY OF CINCINNATI · PI XU, MING · 2005 to 2010
$1.6M
Role of D3 dopamine receptor in behavioral sensitizationR01DA016778 · NIDA · UNIVERSITY OF CINCINNATI · PI RICHTAND, NEIL MARK · 2004 to 2007
$1.2M
D1 DOPAMINE RECEPTOR SIGNALING AND EFFECTS OF COCAINER29DA011284 · NIDA · UNIVERSITY OF CINCINNATI · PI ZHANG, JIANHUA · 1997 to 2001
$214k
NIDA NIH HHS DA016778-01NIDA NIH HHS DA11284NIDA NIH HHS DA14644NIDA NIH HHS DA17323NIDA NIH HHS R01 DA014644NIDA NIH HHS R01 DA016778NIDA NIH HHS R01 DA017323
6 · The paper itself

Abstract

Accumulating evidence suggests that dopamine D3 receptor (D3R) stimulation is inhibitory to spontaneous and psychostimulant-induced locomotion through opposition of concurrent D1R and D2R-mediated signaling. To evaluate this model, we used homozygous D3R mutant mice and wild-type controls to investigate the role of the D3R in locomotor activity and stereotypy stimulated by acute amphetamine (AMPH) (0.2, 2.5, 5.0, 10.0 mg/kg). At the lowest dose tested (0.2 mg/kg), neither D3R mutant mice nor wild-type mice exhibited measurable change in locomotor activity or stereotypy relative to their respective saline-treated controls. D3R mutant mice exhibited a significantly greater increase in locomotor activity, but not stereotypy, relative to wild-type mice in response to treatment with AMPH 2.5 mg/kg. AMPH-induced locomotor activity and stereotypy were similar in both wild-type and D3R mutant mice at both the 5.0 and 10 mg/kg AMPH doses. These findings provide further support for an inhibitory role for the D3R in AMPH-induced locomotor activity, and demonstrate a more limited role for the D3R in modulating AMPH-induced stereotypy.

Indexed as

AmphetamineAnimalsBrainBrain ChemistryDisease Models, AnimalDopamineDopamine AgentsDose-Response Relationship, DrugMaleMiceMice, Inbred C57BLMice, KnockoutMotor ActivityNeural InhibitionReceptors, Dopamine D3Stereotypic Movement DisorderAmphetamineDopamineDopamine AgentsReceptors, Dopamine D3

Identifiers

PMID16856172
PMCPMC1815379
OpenAlexW1969579537

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.