Cited by 86Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental DisordersNeurotransmitter Receptor Influence on Behavior

Social Isolation During the Critical Period Reduces Synaptic and Intrinsic Excitability of a Subtype of Pyramidal Cell in Mouse Prefrontal Cortex

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Yamamuro, Kazuhiko, Yoshino, Hiroki, Ogawa, Yoichi, Makinodan, Manabu, Toritsuka, Michihiro, Yamashita, Masayuki, Corfas, Gabriel, Kishimoto, Toshifumi·2018·Cerebral Cortex

Abstract

Juvenile social experience is crucial for the functional development of forebrain regions, especially the prefrontal cortex (PFC). We previously reported that social isolation for 2 weeks after weaning induces prefrontal cortex dysfunction and hypomyelination. However, the effect of social isolation on physiological properties of PFC neuronal circuit remained unknown. Since hypomyelination due to isolation is prominent in deep-layer of medial PFC (mPFC), we focused on 2 types of Layer-5 pyramidal cells in the mPFC: prominent h-current (PH) cells and nonprominent h-current (non-PH) cells. We found that a 2-week social isolation after weaning leads to a specific deterioration in action potential properties and reduction in excitatory synaptic inputs in PH cells. The effects of social isolation on PH cells, which involve reduction in functional glutamatergic synapses and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid/N-methyl-d-aspartate charge ratio, are specific to the 2 weeks after weaning and to the mPFC. We conclude that juvenile social experience plays crucial roles in the functional development in a subtype of Layer-5 pyramidal cells in the mPFC. Since these neurons project to subcortical structures, a deficit in social experience during the critical period may result in immature neural circuitry between mPFC and subcortical targets.

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  • In rodents, depending on the duration of juvenile social isolation, increased or decreased sociability in adulthood has been reported, suggesting that adolescence is a sensitive period for establishing social behavior later in life.

    “In rodents, depending on the duration of juvenile social isolation, increased or decreased sociability in adulthood has been reported, suggesting that adolescence is a sensitive period for establishing social behavior later in life (Yamamuro et al., 2020; Yamamuro et al., 2018; Makinodan et al., 2012; Rivera-Irizarry et al., 2020).”

    From Oxytocin neurons mediate the effect of social isolation via the VTA circuits (2022) · cites this paper as Yamamuro et al., 2018

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References 54 · Cited by 86

Authors
Yamamuro, K., Yoshino, H., Ogawa, Y., Makinodan, M., Toritsuka, M., Yamashita, M., Corfas, G., & Kishimoto, T.
Affiliations
  • Nara Medical University (JP)
  • International University of Health and Welfare (JP)
  • University of Michigan (US)
  • Department of Psychiatry, Nara Medical University, Kashihara, Nara 634-8522, Japan
Corresponding author
Yoshino, Hiroki
Venue
Cerebral Cortex
Published
2017-02-03
Volume
28
Issue
3
Pages
998-1010
ISSN
  • 1047-3211 (ISSN-L)
  • 1460-2199
OpenAlex
W2584673575
Cited by
86
References
54
Citations by year
2026: 9 · 2025: 8 · 2024: 9 · 2023: 12 · 2022: 13 · 2021: 9 · 2020: 12 · 2019: 6 · 2018: 6 · 2017: 2
FWCI
3.48
Type
journal article
Language
en
Open access
Locations
  • Cerebral Cortex (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Grant-in-Aid for Scientific Research C (25461778)
  • Challenging Exploratory research (15K15432)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Keywords
social isolation, medial prefrontal cortex, layer 5 pyramidal cells, excitability, synaptic excitability, glutamatergic synapses, action potential properties, critical period, hypomyelination, neural circuit development
MeSH terms
Action Potentials, Animals, Animals, Newborn, Critical Period, Psychological, Electric Stimulation, Male, Mice, Inbred C57BL, Social Isolation, Synapses, Tetrodotoxin, Prefrontal Cortex, Pyramidal Cells, Receptors, AMPA, Patch-Clamp Techniques, Excitatory Amino Acid Antagonists, 6-Cyano-7-nitroquinoxaline-2,3-dione, Excitatory Postsynaptic Potentials, Mice, In Vitro Techniques

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