Evidence map›Paper›PMID 36692676›Full record

ReviewMolecular biology reports2023

Understanding translational research in schizophrenia: A novel insight into animal models.

Jonaid Ahmad Malik, Zahid Yaseen, Lahari Thotapalli, Sakeel Ahmed, Mohd Farooq Shaikh, Sirajudheen Anwar

Erratum issuedOpen access · hybridFull text readReview
In one paragraph

Review in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  6. N-acetyl cysteine through modulation of HDACIBRO neuroscience reports · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 6 institutions in 4 countries.

Jonaid Ahmad MalikDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research, Guwahati, India.
Zahid YaseenDepartment of Pharmaceutical Biotechnology, Delhi Pharmaceutical Sciences and Research University, Delhi, India.
Lahari ThotapalliDepartment of Pharmaceutical Sciences, JNTU University, Anantapur, India.
Sakeel AhmedDepartment of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research, Ahmedabad, Gujarat, 382355, India.
Mohd Farooq ShaikhNeuropharmacology Research Strength, Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia, 47500, Bandar Sunway, Selangor, Malaysia. farooq.shaikh@monash.edu.ORCID http://orcid.org/0000-0001-9865-6224
Sirajudheen AnwarDepartment of Pharmacology, College of Pharmacy, University of Hail, Hail, 81422, Saudi Arabia. si.anwar@uoh.edu.
Delhi Pharmaceutical Science and Research University · INIndian Institute of Technology Ropar · INJawaharlal Nehru Technological University Anantapur · INMonash University Malaysia · MYNational Institute of Pharmaceutical Education and Research (NIPER) - Ahmedabad · INUniversity of Ha'il · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schizophrenia affects millions of people worldwide and is a major challenge for the scientific community. Like most psychotic diseases, it is also considered a complicated mental disorder caused by an imbalance in neurotransmitters. Due to the complexity of neuropathology, it is always a complicated disorder. The lack of proper understanding of the pathophysiology makes the disorder unmanageable in clinical settings. However, due to recent advances in animal models, we hope we can have better therapeutic approaches with more success in clinical settings. Dopamine, glutamate, GABA, and serotonin are the neurotransmitters involved in the pathophysiology of schizophrenia. Various animal models have been put forward based on these neurotransmitters, including pharmacological, neurodevelopmental, and genetic models. Polymorphism of genes such as dysbindin, DICS1, and NRG1 has also been reported in schizophrenia. Hypothesis based on dopamine, glutamate, and serotonin are considered successful models of schizophrenia on which drug therapies have been designed to date. New targets like the orexin system, muscarinic and nicotinic receptors, and cannabinoid receptors have been approached to alleviate the negative and cognitive symptoms. The non-pharmacological models like the post-weaning social isolation model (maternal deprivation), the isolation rearing model etc. have been also developed to mimic the symptoms of schizophrenia and to create and test new approaches of drug therapy which is a breakthrough at present in psychiatric disorders. Different behavioral tests have been evaluated in these specific models. This review will highlight the currently available animal models and behavioral tests in psychic disorders concerning schizophrenia.

Indexed as

SchizophreniaAnimalsDisease Models, AnimalDopamineGlutamic AcidSerotoninTranslational Research, BiomedicalDopamineGlutamic AcidSerotoninAnimal modelsAnimal models of schizophreniaPsychotic diseasesSchizophreniaSchizophrenia models

Identifiers

PMID36692676
PMCPMC10042983
OpenAlexW4317869765

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read35
identifiers read8
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.