Evidence map›Paper›PMID 28828223›Full record

ArticleBrain and behavior2017

Effects of haloperidol, olanzapine, ziprasidone, and PHA-543613 on spatial learning and memory in the Morris water maze test in naïve and MK-801-treated mice.

Houxu Ning, Dong Cao, Haidong Wang, Bing Kang, Shiping Xie, Yujing Meng

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

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  6. Developmental Manipulation-Induced Changes in Cognitive Functioning.Current topics in behavioral neurosciences · 2023
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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

6 authors at 3 institutions in 1 country.

Houxu NingDepartment of Psychiatry of Chinese Medicine Affiliated Nanjing Brain Hospital of Nanjing Medical University Nanjing China.ORCID 0000-0002-4326-4706
Dong CaoDepartment of Psychiatry Affiliated Nanjing Brain Hospital of Nanjing Medical University Nanjing China.
Haidong WangDepartment of Psychiatry of Chinese Medicine Affiliated Nanjing Brain Hospital of Nanjing Medical University Nanjing China.
Bing KangDepartment of Psychiatry of Chinese Medicine Affiliated Nanjing Brain Hospital of Nanjing Medical University Nanjing China.
Shiping XieDepartment of Psychiatry Affiliated Nanjing Brain Hospital of Nanjing Medical University Nanjing China.
Yujing MengDepartment of Psychiatry Nanjing Medical University Nanjing China.
Nanjing University of Chinese Medicine · CNNanjing Brain Hospital · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCognitive impairment is the core symptom of schizophrenia, significantly impacting the functional outcome. Improvement of cognitive function has been an important aspect of the treatment of schizophrenia. Therefore, this study is to demonstrate the effects of first-generation antipsychotic haloperidol, second-generation antipsychotic olanzapine and ziprasidone, and alpha-7 nicotinic acetylcholine receptor agonist PHA-543613 on spatial learning and memory. MATERIAL AND

methodsC57BL/6 mice received intraperitoneal injections of haloperidol (2 mg/kg), olanzapine (2.5 mg/kg), ziprasidone (2 mg/kg), and PHA-543613 (1 mg/kg), and cognitive dysfunctions were induced by MK-801 (0.1 mg/kg). Morris water maze was used for investigating the effects of all agents.

resultsMk-801 significantly increased the mean escape latency to the platform and decreased the number of platform area crossings. Ziprasidone had no effect on the mean escape latency to platform and the number of platform area crossings in naïve mice, but haloperidol, olanzapine, and PHA-543613 did not. Haloperidol and olanzapine significantly increased the mean escape latency to platform and decreased the number of platform area crossings, while ziprasidone and PHA-543613 did not. All the agents had no effect on swimming speed.

conclusionsZiprasidone and alpha-7 nicotinic acetylcholine receptor agonist PHA-543613 might be helpful in the treatment of CIAS.

Indexed as

AnimalsAntipsychotic AgentsBenzodiazepinesBridged Bicyclo Compounds, HeterocyclicDisease Models, AnimalHaloperidolMaleMaze LearningMemoryMiceMice, Inbred C57BLOlanzapinePiperazinesQuinuclidinesSchizophreniaSpatial LearningAntipsychotic AgentsBenzodiazepinesBridged Bicyclo Compounds, HeterocyclicHaloperidolN-(1-azabicyclo(2.2.2)oct-3-yl)furo(2,3-c)pyridine-5-carboxamideOlanzapinePiperazinesQuinuclidinesThiazolesziprasidonehaloperidolmiceMK‐801Morris water mazeolanzapinePHA‐543613RRID: SCR_014289ziprasidone

Identifiers

PMID28828223
PMCPMC5561323
OpenAlexW2736066179

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.