Cited by 33Neuroscience and Neuropharmacology ResearchNeurotransmitter Receptor Influence on BehaviorNeurogenesis and neuroplasticity mechanisms

Subtype specific roles of serotonin receptors in the spine formation of cortical neurons in vitro

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Yoshida, Hiroyuki, Kanamaru, Chisako, Ohtani, Akiko, Li, Fei, Senzaki, Kouji, Shiga, Takashi·2011·Neuroscience Research

Abstract

Dendritic spines are postsynaptic structures which are formed from filopodia. We examined roles of serotonin (5-HT) receptors in the spine formation. Embryonic rat cortical neurons were cultured for 10 or 14 days and treated by 5-HT receptor agonists for 24 h. At 11 days in vitro, 5-HT(1A) agonist increased filopodia density, whereas 5-HT(2A/2C) agonist increased the density of puncta and spines. At 15 days in vitro, 5-HT(1A) agonist decreased the density of puncta and spines, whereas 5-HT(2A/2C) agonist decreased filopodia density with increase of spines. In conclusion, the present study shows 5-HT receptors have subtype-specific effects on the spine formation.

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Crossref · 10.1016/j.neures.2011.07.1824

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  • DOI increases synaptic puncta in cultured cortical neurons.

    “DOI, one of the more readily accessible psychedelics to researchers, has been shown to increase dendritic growth (Persico et al., 2006;Ohtani et al., 2014;Ly, Greb et al., 2018;Ly et al., 2021), synaptic puncta, spine density (Yoshida et al., 2011;Ly et al., 2018), and spine size (Jones et al., 2009) in cultured cortical neurons.”

    From Psychedelics and Neural Plasticity: Therapeutic Implications (2022) · cites this paper as Yoshida et al., 2011

  • DOI increases spine density in cultured cortical neurons.

    “DOI, one of the more readily accessible psychedelics to researchers, has been shown to increase dendritic growth (Persico et al., 2006;Ohtani et al., 2014;Ly, Greb et al., 2018;Ly et al., 2021), synaptic puncta, spine density (Yoshida et al., 2011;Ly et al., 2018), and spine size (Jones et al., 2009) in cultured cortical neurons.”

    From Psychedelics and Neural Plasticity: Therapeutic Implications (2022) · cites this paper as Yoshida et al., 2011

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Authors
Yoshida, H., Kanamaru, C., Ohtani, A., Li, F., Senzaki, K., & Shiga, T.
Affiliations
University of Tsukuba (JP)
Corresponding author
Shiga, Takashi
Venue
Neuroscience Research
Publisher
Elsevier BV
Published
2011-11
Volume
71
Issue
3
Pages
311-314
ISSN
0168-0102 (ISSN-L)
OpenAlex
W1967868449
Cited by
33
References
2
Citations by year
2026: 4 · 2024: 1 · 2023: 3 · 2022: 4 · 2021: 3 · 2020: 4 · 2019: 1 · 2018: 1 · 2017: 2 · 2016: 2 · 2015: 2 · 2014: 4 · 2013: 1 · 2012: 1
FWCI
0.79
Type
journal article
Language
en
Open access
Locations
  • Neuroscience Research (publishedVersion)
  • PubMed (publishedVersion)
  • Terrestrial Environment Research Center (University of Tsukuba) (publishedVersion)
  • Institutional Repositories DataBase (IRDB) (acceptedVersion)
Funders
  • Ministry of Education, Culture, Sports, Science and Technology
  • Lupus Research Institute
  • Japan Chemical Industry Association
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords
serotonin receptors, dendritic spine formation, filopodia, 5-HT1A receptor, 5-HT2A/2C receptors, cortical neurons, postsynaptic structures, receptor subtype specificity, serotonin receptor agonists
MeSH terms
Animals, Cell Differentiation, Cerebral Cortex, Neurons, Receptors, Serotonin, Rats, Wistar, Receptor, Serotonin, 5-HT1A, Receptor, Serotonin, 5-HT2A, Receptor, Serotonin, 5-HT2C, Dendritic Spines, Rats, Neurogenesis, Primary Cell Culture

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