Cargando…

Serotonergic Modulation of Locomotor Activity From Basal Vertebrates to Mammals

During the last 50 years, the serotonergic (5-HT) system was reported to exert a complex modulation of locomotor activity. Here, we focus on two key factors that likely contribute to such complexity. First, locomotion is modulated directly and indirectly by 5-HT neurons. The locomotor circuitry is d...

Descripción completa

Detalles Bibliográficos
Autores principales: Flaive, Aurélie, Fougère, Maxime, van der Zouwen, Cornelis Immanuel, Ryczko, Dimitri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674590/
https://www.ncbi.nlm.nih.gov/pubmed/33224027
http://dx.doi.org/10.3389/fncir.2020.590299
_version_ 1783611535439953920
author Flaive, Aurélie
Fougère, Maxime
van der Zouwen, Cornelis Immanuel
Ryczko, Dimitri
author_facet Flaive, Aurélie
Fougère, Maxime
van der Zouwen, Cornelis Immanuel
Ryczko, Dimitri
author_sort Flaive, Aurélie
collection PubMed
description During the last 50 years, the serotonergic (5-HT) system was reported to exert a complex modulation of locomotor activity. Here, we focus on two key factors that likely contribute to such complexity. First, locomotion is modulated directly and indirectly by 5-HT neurons. The locomotor circuitry is directly innervated by 5-HT neurons in the caudal brainstem and spinal cord. Also, indirect control of locomotor activity results from ascending projections of 5-HT cells in the rostral brainstem that innervate multiple brain centers involved in motor action planning. Second, each approach used to manipulate the 5-HT system likely engages different 5-HT-dependent mechanisms. This includes the recruitment of different 5-HT receptors, which can have excitatory or inhibitory effects on cell activity. These receptors can be located far or close to the 5-HT release sites, making their activation dependent on the level of 5-HT released. Here we review the activity of different 5-HT nuclei during locomotor activity, and the locomotor effects of 5-HT precursors, exogenous 5-HT, selective 5-HT reuptake inhibitors (SSRI), electrical or chemical stimulation of 5-HT neurons, genetic deletions, optogenetic and chemogenetic manipulations. We highlight both the coherent and controversial aspects of 5-HT modulation of locomotor activity from basal vertebrates to mammals. This mini review may hopefully inspire future studies aiming at dissecting the complex effects of 5-HT on locomotor function.
format Online
Article
Text
id pubmed-7674590
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-76745902020-11-19 Serotonergic Modulation of Locomotor Activity From Basal Vertebrates to Mammals Flaive, Aurélie Fougère, Maxime van der Zouwen, Cornelis Immanuel Ryczko, Dimitri Front Neural Circuits Neuroscience During the last 50 years, the serotonergic (5-HT) system was reported to exert a complex modulation of locomotor activity. Here, we focus on two key factors that likely contribute to such complexity. First, locomotion is modulated directly and indirectly by 5-HT neurons. The locomotor circuitry is directly innervated by 5-HT neurons in the caudal brainstem and spinal cord. Also, indirect control of locomotor activity results from ascending projections of 5-HT cells in the rostral brainstem that innervate multiple brain centers involved in motor action planning. Second, each approach used to manipulate the 5-HT system likely engages different 5-HT-dependent mechanisms. This includes the recruitment of different 5-HT receptors, which can have excitatory or inhibitory effects on cell activity. These receptors can be located far or close to the 5-HT release sites, making their activation dependent on the level of 5-HT released. Here we review the activity of different 5-HT nuclei during locomotor activity, and the locomotor effects of 5-HT precursors, exogenous 5-HT, selective 5-HT reuptake inhibitors (SSRI), electrical or chemical stimulation of 5-HT neurons, genetic deletions, optogenetic and chemogenetic manipulations. We highlight both the coherent and controversial aspects of 5-HT modulation of locomotor activity from basal vertebrates to mammals. This mini review may hopefully inspire future studies aiming at dissecting the complex effects of 5-HT on locomotor function. Frontiers Media S.A. 2020-11-05 /pmc/articles/PMC7674590/ /pubmed/33224027 http://dx.doi.org/10.3389/fncir.2020.590299 Text en Copyright © 2020 Flaive, Fougère, van der Zouwen and Ryczko. http://creativecommons.org/licenses/by/4.0/ 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) and the copyright owner(s) 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
Flaive, Aurélie
Fougère, Maxime
van der Zouwen, Cornelis Immanuel
Ryczko, Dimitri
Serotonergic Modulation of Locomotor Activity From Basal Vertebrates to Mammals
title Serotonergic Modulation of Locomotor Activity From Basal Vertebrates to Mammals
title_full Serotonergic Modulation of Locomotor Activity From Basal Vertebrates to Mammals
title_fullStr Serotonergic Modulation of Locomotor Activity From Basal Vertebrates to Mammals
title_full_unstemmed Serotonergic Modulation of Locomotor Activity From Basal Vertebrates to Mammals
title_short Serotonergic Modulation of Locomotor Activity From Basal Vertebrates to Mammals
title_sort serotonergic modulation of locomotor activity from basal vertebrates to mammals
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674590/
https://www.ncbi.nlm.nih.gov/pubmed/33224027
http://dx.doi.org/10.3389/fncir.2020.590299
work_keys_str_mv AT flaiveaurelie serotonergicmodulationoflocomotoractivityfrombasalvertebratestomammals
AT fougeremaxime serotonergicmodulationoflocomotoractivityfrombasalvertebratestomammals
AT vanderzouwencornelisimmanuel serotonergicmodulationoflocomotoractivityfrombasalvertebratestomammals
AT ryczkodimitri serotonergicmodulationoflocomotoractivityfrombasalvertebratestomammals