Evidence map›Paper›PMID 29417763›Full record

ArticlePharmacology research & perspectives2018

Combined treatment with a selective PDE10A inhibitor TAK-063 and either haloperidol or olanzapine at subeffective doses produces potent antipsychotic-like effects without affecting plasma prolactin levels and cataleptic responses in rodents.

Kazunori Suzuki, Akina Harada, Hirobumi Suzuki, Clizia Capuani, Annarosa Ugolini, Mauro Corsi, Haruhide Kimura

Abstract read
In one paragraph

Article in Pharmacology research & perspectives, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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  7. 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

7 authors.

Kazunori SuzukiCNS Drug Discovery Unit, Research, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa, Japan.ORCID 0000-0002-9584-1974
Akina HaradaCNS Drug Discovery Unit, Research, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa, Japan.
Hirobumi SuzukiCNS Drug Discovery Unit, Research, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa, Japan.
Clizia CapuaniCenter for Drug Design & Discovery, Aptuit Inc., Verona, Italy.
Annarosa UgoliniCenter for Drug Design & Discovery, Aptuit Inc., Verona, Italy.
Mauro CorsiCenter for Drug Design & Discovery, Aptuit Inc., Verona, Italy.
Haruhide KimuraCNS Drug Discovery Unit, Research, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa, Japan.ORCID 0000-0002-8292-3647

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Activation of indirect pathway medium spiny neurons (MSNs) via promotion of cAMP production is the principal mechanism of action of current antipsychotics with dopamine D

Indexed as

Administration, OralAkathisia, Drug-InducedAnimalsAntipsychotic AgentsBenzodiazepinesCatalepsyCorpus StriatumDendritic SpinesDisease Models, AnimalDopamine AntagonistsDrug SynergismDrug Therapy, CombinationHaloperidolHumansMaleMethamphetamine1-(2-fluoro-4-(1H-pyrazol-1-yl)phenyl)-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-oneAntipsychotic AgentsBenzodiazepinesDopamine AntagonistsHaloperidolMethamphetamineOlanzapinePhosphodiesterase InhibitorsProlactinPyrazolesPyridazinesantipsychoticsmedium spiny neuronphosphodiesterase 10AschizophreniaTAK-063

Identifiers

PMID29417763
PMCPMC5817828

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.