Selective serotonin reuptake inhibitors induce spontaneous interneuronal activity in the leech nervous system

Serotonin [5-hydroxytryptamine (5-HT)] is a conspicuous neuromodulator of sensory-motor networks that affects a variety of neurons at different levels of the network hierarchy. Because of its many possible targets, it has been difficult to obtain a comprehensive picture of how 5-HT achieves its fina...

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Autores principales: Calviño, M.A., Iscla, I.R., Szczupak, L.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00223077_v93_n5_p2644_Calvino
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spelling todo:paper_00223077_v93_n5_p2644_Calvino2023-10-03T14:31:00Z Selective serotonin reuptake inhibitors induce spontaneous interneuronal activity in the leech nervous system Calviño, M.A. Iscla, I.R. Szczupak, L. citalopram clomipramine fluoxetine imipramine serotonin serotonin uptake inhibitor tricyclic antidepressant agent animal cell animal experiment article controlled study data analysis electrophysiology ganglion interneuron leech motor system nerve cell nervous system nonhuman priority journal sensory system synaptic potential Action Potentials Adrenergic Uptake Inhibitors Animals Citalopram Drug Interactions Electric Stimulation Fluoxetine Ganglia, Invertebrate Imipramine Interneurons Leeches Membrane Potentials Neural Networks (Computer) Paroxetine Serotonin Serotonin Uptake Inhibitors Synapses Serotonin [5-hydroxytryptamine (5-HT)] is a conspicuous neuromodulator of sensory-motor networks that affects a variety of neurons at different levels of the network hierarchy. Because of its many possible targets, it has been difficult to obtain a comprehensive picture of how 5-HT achieves its final modulatory output on any given network. Our hypothesis is that the profile of 5-HT actions is dictated by its pattern of release from endogenous sites. We tested this hypothesis in the leech nervous system by means of a selective serotonin reuptake blocker (SSRI), fluoxetine. Fluoxetine evoked barrages of synaptic potentials in identified sensory, motor, and interneurons. This effect was mimicked by the tricyclic antidepressants imipramine and clomipramine, and by the SSRI citalopram, with relative efficacies that matched their known relative selectivities for the 5-HT transporter. The synaptic responses evoked by fluoxetine in different neurons were temporally correlated, suggesting that they had a common origin. The profile of the synaptic responses matched that expected from the activation of the mechanosensory pressure cells, known to act by polysynaptic pathways. The results suggest that endogenous 5-HT acted on cord spanning interneurons. On the other hand, bath-applied 5-HT evoked an effect different from that of the SSRI. Taken together, the results evidenced that the pattern of action of the monoamine is dictated by the spatial distribution of the 5-HT release sites. Copyright © 2005 The American Physiological Society. Fil:Calviño, M.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Iscla, I.R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Szczupak, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00223077_v93_n5_p2644_Calvino
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic citalopram
clomipramine
fluoxetine
imipramine
serotonin
serotonin uptake inhibitor
tricyclic antidepressant agent
animal cell
animal experiment
article
controlled study
data analysis
electrophysiology
ganglion
interneuron
leech
motor system
nerve cell
nervous system
nonhuman
priority journal
sensory system
synaptic potential
Action Potentials
Adrenergic Uptake Inhibitors
Animals
Citalopram
Drug Interactions
Electric Stimulation
Fluoxetine
Ganglia, Invertebrate
Imipramine
Interneurons
Leeches
Membrane Potentials
Neural Networks (Computer)
Paroxetine
Serotonin
Serotonin Uptake Inhibitors
Synapses
spellingShingle citalopram
clomipramine
fluoxetine
imipramine
serotonin
serotonin uptake inhibitor
tricyclic antidepressant agent
animal cell
animal experiment
article
controlled study
data analysis
electrophysiology
ganglion
interneuron
leech
motor system
nerve cell
nervous system
nonhuman
priority journal
sensory system
synaptic potential
Action Potentials
Adrenergic Uptake Inhibitors
Animals
Citalopram
Drug Interactions
Electric Stimulation
Fluoxetine
Ganglia, Invertebrate
Imipramine
Interneurons
Leeches
Membrane Potentials
Neural Networks (Computer)
Paroxetine
Serotonin
Serotonin Uptake Inhibitors
Synapses
Calviño, M.A.
Iscla, I.R.
Szczupak, L.
Selective serotonin reuptake inhibitors induce spontaneous interneuronal activity in the leech nervous system
topic_facet citalopram
clomipramine
fluoxetine
imipramine
serotonin
serotonin uptake inhibitor
tricyclic antidepressant agent
animal cell
animal experiment
article
controlled study
data analysis
electrophysiology
ganglion
interneuron
leech
motor system
nerve cell
nervous system
nonhuman
priority journal
sensory system
synaptic potential
Action Potentials
Adrenergic Uptake Inhibitors
Animals
Citalopram
Drug Interactions
Electric Stimulation
Fluoxetine
Ganglia, Invertebrate
Imipramine
Interneurons
Leeches
Membrane Potentials
Neural Networks (Computer)
Paroxetine
Serotonin
Serotonin Uptake Inhibitors
Synapses
description Serotonin [5-hydroxytryptamine (5-HT)] is a conspicuous neuromodulator of sensory-motor networks that affects a variety of neurons at different levels of the network hierarchy. Because of its many possible targets, it has been difficult to obtain a comprehensive picture of how 5-HT achieves its final modulatory output on any given network. Our hypothesis is that the profile of 5-HT actions is dictated by its pattern of release from endogenous sites. We tested this hypothesis in the leech nervous system by means of a selective serotonin reuptake blocker (SSRI), fluoxetine. Fluoxetine evoked barrages of synaptic potentials in identified sensory, motor, and interneurons. This effect was mimicked by the tricyclic antidepressants imipramine and clomipramine, and by the SSRI citalopram, with relative efficacies that matched their known relative selectivities for the 5-HT transporter. The synaptic responses evoked by fluoxetine in different neurons were temporally correlated, suggesting that they had a common origin. The profile of the synaptic responses matched that expected from the activation of the mechanosensory pressure cells, known to act by polysynaptic pathways. The results suggest that endogenous 5-HT acted on cord spanning interneurons. On the other hand, bath-applied 5-HT evoked an effect different from that of the SSRI. Taken together, the results evidenced that the pattern of action of the monoamine is dictated by the spatial distribution of the 5-HT release sites. Copyright © 2005 The American Physiological Society.
format JOUR
author Calviño, M.A.
Iscla, I.R.
Szczupak, L.
author_facet Calviño, M.A.
Iscla, I.R.
Szczupak, L.
author_sort Calviño, M.A.
title Selective serotonin reuptake inhibitors induce spontaneous interneuronal activity in the leech nervous system
title_short Selective serotonin reuptake inhibitors induce spontaneous interneuronal activity in the leech nervous system
title_full Selective serotonin reuptake inhibitors induce spontaneous interneuronal activity in the leech nervous system
title_fullStr Selective serotonin reuptake inhibitors induce spontaneous interneuronal activity in the leech nervous system
title_full_unstemmed Selective serotonin reuptake inhibitors induce spontaneous interneuronal activity in the leech nervous system
title_sort selective serotonin reuptake inhibitors induce spontaneous interneuronal activity in the leech nervous system
url http://hdl.handle.net/20.500.12110/paper_00223077_v93_n5_p2644_Calvino
work_keys_str_mv AT calvinoma selectiveserotoninreuptakeinhibitorsinducespontaneousinterneuronalactivityintheleechnervoussystem
AT isclair selectiveserotoninreuptakeinhibitorsinducespontaneousinterneuronalactivityintheleechnervoussystem
AT szczupakl selectiveserotoninreuptakeinhibitorsinducespontaneousinterneuronalactivityintheleechnervoussystem
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