Evidence map›Paper›PMID 38903649›Full record

ArticleFrontiers in psychiatry2024

NARP-related alterations in the excitatory and inhibitory circuitry of socially isolated mice: developmental insights and implications for autism spectrum disorder.

Yasunari Yamaguchi, Kazuya Okamura, Kazuhiko Yamamuro, Kazuki Okumura, Takashi Komori, Michihiro Toritsuka, Ryohei Takada, Yosuke Nishihata, Daisuke Ikawa, Takahira Yamauchi and 6 more

Abstract read
In one paragraph

Article in Frontiers in psychiatry, 2024. 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

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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. Review
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

16 authors.

Yasunari Yamaguchi *Department of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Kazuya Okamura *Department of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Kazuhiko YamamuroDepartment of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Kazuki OkumuraDepartment of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Takashi KomoriDepartment of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Michihiro ToritsukaDepartment of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Ryohei TakadaDepartment of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Yosuke NishihataDepartment of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Daisuke IkawaDepartment of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Takahira YamauchiDepartment of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Manabu MakinodanDepartment of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Hiroki YoshinoDepartment of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Yasuhiko SaitoDepartment of Neurophysiology, Nara Medical University School of Medicine, Nara, Japan.
Hideo MatsuzakiResearch Center for Child Mental Development, University of Fukui, Fukui, Japan.
Toshifumi KishimotoDepartment of Psychiatry, Nara Medical University School of Medicine, Nara, Japan.
Sohei KimotoDepartment of Neuropsychiatry, Wakayama Medical University School of Medicine, Wakayama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Social isolation during critical periods of development is associated with alterations in behavior and neuronal circuitry. This study aimed to investigate the immediate and developmental effects of social isolation on firing properties, neuronal activity-regulated pentraxin (NARP) and parvalbumin (PV) expression in the prefrontal cortex (PFC), social behavior in juvenile socially isolated mice, and the biological relevance of NARP expression in autism spectrum disorder (ASD). Methods: Mice were subjected to social isolation during postnatal days 21-35 (P21-P35) and were compared with group-housed control mice. Firing properties in the PFC pyramidal neurons were altered in P35 socially isolated mice, which might be associated with alterations in NARP and PV expression. Results: In adulthood, mice that underwent juvenile social isolation exhibited difficulty distinguishing between novel and familiar mice during a social memory task, while maintaining similar levels of social interaction as the control mice. Furthermore, a marked decrease in NARP expression in lymphoblastoid cell lines derived from adolescent humans with ASD as compared to typically developing (TD) humans was found. Conclusion: Our study highlights the role of electrophysiological properties, as well as NARP and PV expression in the PFC in mediating the developmental consequences of social isolation on behavior.

Indexed as

autism spectrum disorder (ASD)brain developmentneuronal activity-regulated pentraxin (NARP)parvalbumin (PV)prefrontal cortex (PFC)social behaviorsocial isolation

Identifiers

PMID38903649
PMCPMC11187327

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