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5-HT(7) receptors as modulators of neuronal excitability, synaptic transmission and plasticity: physiological role and possible implications in autism spectrum disorders
Serotonin type 7 receptors (5-HT(7)) are expressed in several brain areas, regulate brain development, synaptic transmission and plasticity, and therefore are involved in various brain functions such as learning and memory. A number of studies suggest that 5-HT(7) receptors could be potential pharma...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145633/ https://www.ncbi.nlm.nih.gov/pubmed/25221471 http://dx.doi.org/10.3389/fncel.2014.00250 |
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author | Ciranna, Lucia Catania, Maria Vincenza |
author_facet | Ciranna, Lucia Catania, Maria Vincenza |
author_sort | Ciranna, Lucia |
collection | PubMed |
description | Serotonin type 7 receptors (5-HT(7)) are expressed in several brain areas, regulate brain development, synaptic transmission and plasticity, and therefore are involved in various brain functions such as learning and memory. A number of studies suggest that 5-HT(7) receptors could be potential pharmacotherapeutic target for cognitive disorders. Several abnormalities of serotonergic system have been described in patients with autism spectrum disorder (ASD), including abnormal activity of 5-HT transporter, altered blood and brain 5-HT levels, reduced 5-HT synthesis and altered expression of 5-HT receptors in the brain. A specific role for 5-HT(7) receptors in ASD has not yet been demonstrated but some evidence implicates their possible involvement. We have recently shown that 5-HT(7) receptor activation rescues hippocampal synaptic plasticity in a mouse model of Fragile X Syndrome, a monogenic cause of autism. Several other studies have shown that 5-HT(7) receptors modulate behavioral flexibility, exploratory behavior, mood disorders and epilepsy, which include core and co-morbid symptoms of ASD. These findings further suggest an involvement of 5-HT(7) receptors in ASD. Here, we review the physiological roles of 5-HT(7) receptors and their implications in Fragile X Syndrome and other ASD. |
format | Online Article Text |
id | pubmed-4145633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41456332014-09-12 5-HT(7) receptors as modulators of neuronal excitability, synaptic transmission and plasticity: physiological role and possible implications in autism spectrum disorders Ciranna, Lucia Catania, Maria Vincenza Front Cell Neurosci Neuroscience Serotonin type 7 receptors (5-HT(7)) are expressed in several brain areas, regulate brain development, synaptic transmission and plasticity, and therefore are involved in various brain functions such as learning and memory. A number of studies suggest that 5-HT(7) receptors could be potential pharmacotherapeutic target for cognitive disorders. Several abnormalities of serotonergic system have been described in patients with autism spectrum disorder (ASD), including abnormal activity of 5-HT transporter, altered blood and brain 5-HT levels, reduced 5-HT synthesis and altered expression of 5-HT receptors in the brain. A specific role for 5-HT(7) receptors in ASD has not yet been demonstrated but some evidence implicates their possible involvement. We have recently shown that 5-HT(7) receptor activation rescues hippocampal synaptic plasticity in a mouse model of Fragile X Syndrome, a monogenic cause of autism. Several other studies have shown that 5-HT(7) receptors modulate behavioral flexibility, exploratory behavior, mood disorders and epilepsy, which include core and co-morbid symptoms of ASD. These findings further suggest an involvement of 5-HT(7) receptors in ASD. Here, we review the physiological roles of 5-HT(7) receptors and their implications in Fragile X Syndrome and other ASD. Frontiers Media S.A. 2014-08-27 /pmc/articles/PMC4145633/ /pubmed/25221471 http://dx.doi.org/10.3389/fncel.2014.00250 Text en Copyright © 2014 Ciranna and Catania. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Ciranna, Lucia Catania, Maria Vincenza 5-HT(7) receptors as modulators of neuronal excitability, synaptic transmission and plasticity: physiological role and possible implications in autism spectrum disorders |
title | 5-HT(7) receptors as modulators of neuronal excitability, synaptic transmission and plasticity: physiological role and possible implications in autism spectrum disorders |
title_full | 5-HT(7) receptors as modulators of neuronal excitability, synaptic transmission and plasticity: physiological role and possible implications in autism spectrum disorders |
title_fullStr | 5-HT(7) receptors as modulators of neuronal excitability, synaptic transmission and plasticity: physiological role and possible implications in autism spectrum disorders |
title_full_unstemmed | 5-HT(7) receptors as modulators of neuronal excitability, synaptic transmission and plasticity: physiological role and possible implications in autism spectrum disorders |
title_short | 5-HT(7) receptors as modulators of neuronal excitability, synaptic transmission and plasticity: physiological role and possible implications in autism spectrum disorders |
title_sort | 5-ht(7) receptors as modulators of neuronal excitability, synaptic transmission and plasticity: physiological role and possible implications in autism spectrum disorders |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145633/ https://www.ncbi.nlm.nih.gov/pubmed/25221471 http://dx.doi.org/10.3389/fncel.2014.00250 |
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