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.
Copyright © 2011 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Cell Differentiation / drug effects
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Cell Differentiation / physiology*
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Cerebral Cortex / cytology*
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Cerebral Cortex / drug effects
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Cerebral Cortex / embryology*
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Dendritic Spines / drug effects
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Dendritic Spines / physiology*
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Neurogenesis / drug effects
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Neurogenesis / physiology*
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Neurons / drug effects
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Neurons / physiology*
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Primary Cell Culture
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Rats
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Rats, Wistar
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Receptor, Serotonin, 5-HT1A / physiology
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Receptor, Serotonin, 5-HT2A / physiology
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Receptor, Serotonin, 5-HT2C / physiology
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Receptors, Serotonin / classification*
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Receptors, Serotonin / physiology*
Substances
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Receptor, Serotonin, 5-HT2A
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Receptor, Serotonin, 5-HT2C
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Receptors, Serotonin
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Receptor, Serotonin, 5-HT1A