Evidence map›Paper›PMID 40796994›Full record

ArticleJournal of molecular neuroscience : MN2025

Effects of Risperidone and Aripiprazole Antipsychotic Drugs on Behavioral Changes and the Expression Levels of DRD2, HTR2A, AKT1, and CACNA1C Genes in the Hippocampus of a Ketamine-induced Schizophrenia-like Rat Model.

Mobin Naderi, Hamed Ghazvini, Amir Maleksabet, Hossein Ghalehnoei, Rezvan Khajavi

Abstract read
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Article in Journal of molecular neuroscience : MN, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

5 authors.

Mobin NaderiStudent Research Committee, Faculty of Advanced Technologies in Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Hamed GhazviniDepartment of Neuroscience, Faculty of Advanced Technologies in Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Amir MaleksabetDepartment of Medical Biotechnology, Faculty of Advanced Technologies in Medicine, Molecular and Cell Biology Research Center, School of Advanced Technologies in Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Hossein GhalehnoeiDepartment of Medical Biotechnology, Faculty of Advanced Technologies in Medicine, Molecular and Cell Biology Research Center, School of Advanced Technologies in Medicine, Mazandaran University of Medical Sciences, Sari, Iran. hossein.ghalehnoei58@gmail.com.
Rezvan KhajaviMolecular and Cell Biology Research Center, Mazandaran University of Medical Sciences, Sari, Iran.

Funding

Mazandaran University of Medical Sciences 18071
6 · The paper itself

Abstract

Schizophrenia, a severe neuropsychiatric disorder, is characterized by significant impairments in neurological function. The disease includes a spectrum of symptoms that are divided into four main categories: positive, negative, cognitive, and mood symptoms. In this study, 32 male Wistar rats, approximately 10 to 12 weeks old, were randomly separated into four groups: vehicle (saline), ketamine (30 mg/kg), aripiprazole (0.75 mg/kg), and risperidone (1 mg/kg). Twenty-four hours following the final ketamine or saline administration, social interaction test (SIT), open field test (OFT), novel object recognition (NOR), and elevated plus-maze (EPM) were performed on the animals. Hippocampal tissue was used for molecular analysis using Real-Time PCR technique. Behavioral tests revealed that both risperidone and aripiprazole reduced anxiety-like behaviors and enhanced cognitive discrimination. At the molecular level, hippocampal expression of DRD2 and HTR2A did not differ significantly across groups. However, the ketamine-treated group exhibited elevated AKT1 expression relative to the vehicle group, whereas risperidone administration downregulated AKT1 compared to the ketamine group. Notably, CACNA1C expression was upregulated in the aripiprazole group compared to both the ketamine and vehicle groups. The findings of this study showed that the antipsychotic drugs risperidone and aripiprazole have the ability to moderately alleviate cognitive deficits in rats. The results also indicated that this treatment may affect the gene expression of AKT1, and CACNA1C genes.

Indexed as

Antipsychotic AgentsAripiprazoleHippocampusRisperidoneSchizophreniaAnimalsCalcium Channels, L-TypeKetamineMaleProto-Oncogene Proteins c-aktRatsRats, WistarReceptors, Dopamine D2Receptor, Serotonin, 5-HT2AAkt1 protein, ratAntipsychotic AgentsAripiprazoleCacna1c protein, ratCalcium Channels, L-TypeDRD2 protein, ratKetamineProto-Oncogene Proteins c-aktReceptors, Dopamine D2Receptor, Serotonin, 5-HT2ARisperidoneAripiprazoleBehavioral testsGene expressionKetamineRatRisperidoneSchizophrenia

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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.