Evidence map›Paper›PMID 41404898›Full record

ArticleThe European journal of neuroscience2025

Conspecific Presence Promotes Social Buffering, Restores Social Reward, and Enhances Spatial Navigation in a Ketamine-Induced Model of Schizophrenia in Mice.

Rayan Fidel Martins Monteiro, Marcos Vinícius Lebrego Nascimento, Klinsmann Thiago Lima, Valdina Solimar Lopes Cardoso, José Ramon Gama Almeida, Wellington Junior Taisho Nagahama Costa, Bruno Eduardo Godinho Teixeira, Vinicius Teles Shirakura, Soraya Amin Souza, Juliana Silva Cassoli and 1 more

Abstract read
In one paragraph

Article in The European journal of neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

11 authors.

Rayan Fidel Martins MonteiroLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Pará, Brazil.
Marcos Vinícius Lebrego NascimentoLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Pará, Brazil.
Klinsmann Thiago LimaLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Pará, Brazil.
Valdina Solimar Lopes CardosoLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Pará, Brazil.
José Ramon Gama AlmeidaLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Pará, Brazil.
Wellington Junior Taisho Nagahama CostaLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Pará, Brazil.
Bruno Eduardo Godinho TeixeiraLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Pará, Brazil.
Vinicius Teles ShirakuraLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Pará, Brazil.
Soraya Amin SouzaLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Pará, Brazil.
Juliana Silva CassoliLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Pará, Brazil.
Gilmara de Nazareth Tavares BastosLaboratory of Neuroinflammation, Institute of Biological Sciences, Federal University of Pará, Belém, Pará, Brazil.ORCID 0000-0002-4899-6500

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)National Council of Scientific and Technological Development (CNPq)
6 · The paper itself

Abstract

Despite extensive research on the effects of enriched environments in mouse models of psychiatric disorders, the role of social context remains poorly explored. Therefore, we assessed the impact of a conspecific during the evaluation of negative and cognitive symptoms in a mouse model of schizophrenia (SCZ). Male C57BL/6J mice received daily injections of ketamine (25 mg/kg) or vehicle. Behavioral testing was conducted with mice either alone or in dyads of varying familiarity. Anxiety-like behavior and habituation were assessed using the 3D maze test (3DM). Social reward was measured with a social conditioned place preference test. Finally, episodic memory was evaluated using an object recognition memory test (ORMT). Ketamine induced anxiogenic-like behavior and impaired habituation, social reward, and spatial memory. In contrast, the presence of a conspecific induced anxiolytic-like behavior, accelerated habituation, and restored social reward. Additionally, greater dyad familiarity led to better performance in the 3DM. Conversely, the presence of a conspecific did not rescue cognitive deficits in the ORMT; however, spatial navigation in the 3DM was improved. These results support that the presence of a conspecific induces social buffering and promotes prosocial behavior. Therefore, this highlights a therapeutic effect modulated by social context and introduces a new model to evaluate social cognition in a mouse model of SCZ.

Indexed as

RewardSchizophreniaSocial BehaviorSpatial NavigationAnimalsAnxietyBehavior, AnimalDisease Models, AnimalKetamineMaleMaze LearningMiceMice, Inbred C57BLRecognition, PsychologyKetamineanxiety‐like behaviorketamineschizophreniasocial bufferingsocial cognition

Identifiers

PMID41404898
PMCPMC12710120

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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.