Evidence map›Paper›PMID 28612134›Full record

ArticlePsychopharmacology2017

Ketamine-induced behavioural and brain oxidative changes in mice: an assessment of possible beneficial effects of zinc as mono- or adjunct therapy.

Olakunle James Onaolapo, Olayemi Quyyom Ademakinwa, Temitayo Opeyemi Olalekan, Adejoke Yetunde Onaolapo

Abstract read
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In one paragraph

Article in Psychopharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Zinc in psychosis (Review).Molecular medicine reports · 2025
    Review
  5. Review
  6. Article
  7. Article
  8. Advantages and Limitations of Animal Schizophrenia Models.International journal of molecular sciences · 2022
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. 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

4 authors at 1 institution in 1 country.

Olakunle James OnaolapoDepartment of Pharmacology, Ladoke Akintola University of Technology, Osogbo, Osun State, Nigeria. olakunleonaolapo@yahoo.co.uk.
Olayemi Quyyom AdemakinwaDepartment of Pharmacology, Ladoke Akintola University of Technology, Osogbo, Osun State, Nigeria.
Temitayo Opeyemi OlalekanDepartment of Anatomy, Ladoke Akintola University of Technology, Ogbomoso, Oyo State, Nigeria.
Adejoke Yetunde OnaolapoDepartment of Anatomy, Ladoke Akintola University of Technology, Ogbomoso, Oyo State, Nigeria. adegbayibiy@yahoo.com.
Ladoke Akintola University of Technology · NG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleWe studied the influence of zinc, haloperidol or olanzapine on neurobehaviour (open-field, radial arm maze and elevated plus maze) and brain antioxidant status in vehicle- or ketamine-treated mice, with the aim of ascertaining the potentials of zinc in counteracting ketamine's effects.

objectivesExperiment 1 assessed the effects of zinc in healthy animals and the relative degrees of modulation of ketamine's effects by zinc, haloperidol or olanzapine, respectively. Experiment 2 assessed the modulation of ketamine's effects following co-administration of zinc with haloperidol or olanzapine.

methodsMale mice weighing 18-20 g each were used. Animals were pretreated with ketamine (except vehicle, zinc, haloperidol and olanzapine controls) for 10 days before commencement of 14-day treatment (day 11-24) with vehicle, zinc, haloperidol or olanzapine (alone or in combination). Ketamine injection also continued alongside zinc and/or standard drugs in the ketamine-treated groups. Zinc, haloperidol and olanzapine were administered by gavage. Treatments were given daily and behaviours assessed on days 11 and 24. On day 24, animals were sacrificed and whole brain homogenates used for estimation of glutathione, nitric oxide and malondialdehyde (MDA) levels.

resultsKetamine increased open-field behaviours, nitric oxide and MDA levels, while it decreased working memory, social interaction and glutathione. Administration of zinc alone or in combination with haloperidol or olanzapine was associated with variable degrees of reversal of these effects.

conclusionZinc may have the potential of a possible therapeutic agent and/or adjunct in the reversal of schizophrenia-like changes in behaviour and brain oxidative status.

Indexed as

Interpersonal RelationsAnesthetics, DissociativeAnimalsAntioxidantsAntipsychotic AgentsBenzodiazepinesBrainDrug Therapy, CombinationHaloperidolKetamineMaleMaze LearningMiceOlanzapineOxidative StressSchizophreniaAnesthetics, DissociativeAntioxidantsAntipsychotic AgentsBenzodiazepinesHaloperidolKetamineOlanzapineZincAntipsychoticKetamineMemoryOxidative stressSchizophreniaSocial interactionTrace element

Identifiers

PMID28612134
OpenAlexW2626119011

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.