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Activity-dependent serotonergic excitation of callosal projection neurons in the mouse prefrontal cortex

Layer 5 pyramidal neurons (L5PNs) in the mouse prefrontal cortex respond to serotonin (5-HT) according to their long-distance axonal projections; 5-HT(1A) (1A) receptors mediate inhibitory responses in corticopontine (CPn) L5PNs, while 5-HT(2A) (2A) receptors can enhance action potential (AP) output...

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Autores principales: Stephens, Emily K., Avesar, Daniel, Gulledge, Allan T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4144257/
https://www.ncbi.nlm.nih.gov/pubmed/25206322
http://dx.doi.org/10.3389/fncir.2014.00097
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author Stephens, Emily K.
Avesar, Daniel
Gulledge, Allan T.
author_facet Stephens, Emily K.
Avesar, Daniel
Gulledge, Allan T.
author_sort Stephens, Emily K.
collection PubMed
description Layer 5 pyramidal neurons (L5PNs) in the mouse prefrontal cortex respond to serotonin (5-HT) according to their long-distance axonal projections; 5-HT(1A) (1A) receptors mediate inhibitory responses in corticopontine (CPn) L5PNs, while 5-HT(2A) (2A) receptors can enhance action potential (AP) output in callosal/commissural (COM) L5PNs, either directly (in “COM-excited” neurons), or following brief 1A-mediated inhibition (in “COM-biphasic” neurons). Here we compare the impact of 5-HT on the excitability of CPn and COM L5PNs experiencing variable excitatory drive produced by current injection (DC current or simulated synaptic current) or with exogenous glutamate. 5-HT delivered at resting membrane potentials, or paired with subthreshold depolarizing input, hyperpolarized CPn and COM-biphasic L5PNs and failed to promote AP generation in COM-excited L5PNs. Conversely, when paired with suprathreshold excitatory drive generating multiple APs, 5-HT suppressed AP output in CPn L5PNs, enhanced AP generation in COM-excited L5PNs, and generated variable responses in COM-biphasic L5PNs. While COM-excited neurons failed to respond to 5-HT in the presence of a 2A receptor antagonist, 32% of CPn neurons exhibited 2A-dependent excitation following blockade of 1A receptors. The presence of pharmacologically revealed 2A receptors in CPn L5PNs was correlated with the duration of 1A-mediated inhibition, yet biphasic excitatory responses to 5-HT were never observed, even when 5-HT was paired with strong excitatory drive. Our results suggest that 2A receptors selectively amplify the output of COM L5PNs experiencing suprathreshold excitatory drive, while shaping the duration of 1A-mediated inhibition in a subset of CPn L5PNs. Activity-dependent serotonergic excitation of COM L5PNs, combined with 1A-mediated inhibition of CPn and COM-biphasic L5PNs, may facilitate executive function by focusing network activity within cortical circuits subserving the most appropriate behavioral output.
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spelling pubmed-41442572014-09-09 Activity-dependent serotonergic excitation of callosal projection neurons in the mouse prefrontal cortex Stephens, Emily K. Avesar, Daniel Gulledge, Allan T. Front Neural Circuits Neuroscience Layer 5 pyramidal neurons (L5PNs) in the mouse prefrontal cortex respond to serotonin (5-HT) according to their long-distance axonal projections; 5-HT(1A) (1A) receptors mediate inhibitory responses in corticopontine (CPn) L5PNs, while 5-HT(2A) (2A) receptors can enhance action potential (AP) output in callosal/commissural (COM) L5PNs, either directly (in “COM-excited” neurons), or following brief 1A-mediated inhibition (in “COM-biphasic” neurons). Here we compare the impact of 5-HT on the excitability of CPn and COM L5PNs experiencing variable excitatory drive produced by current injection (DC current or simulated synaptic current) or with exogenous glutamate. 5-HT delivered at resting membrane potentials, or paired with subthreshold depolarizing input, hyperpolarized CPn and COM-biphasic L5PNs and failed to promote AP generation in COM-excited L5PNs. Conversely, when paired with suprathreshold excitatory drive generating multiple APs, 5-HT suppressed AP output in CPn L5PNs, enhanced AP generation in COM-excited L5PNs, and generated variable responses in COM-biphasic L5PNs. While COM-excited neurons failed to respond to 5-HT in the presence of a 2A receptor antagonist, 32% of CPn neurons exhibited 2A-dependent excitation following blockade of 1A receptors. The presence of pharmacologically revealed 2A receptors in CPn L5PNs was correlated with the duration of 1A-mediated inhibition, yet biphasic excitatory responses to 5-HT were never observed, even when 5-HT was paired with strong excitatory drive. Our results suggest that 2A receptors selectively amplify the output of COM L5PNs experiencing suprathreshold excitatory drive, while shaping the duration of 1A-mediated inhibition in a subset of CPn L5PNs. Activity-dependent serotonergic excitation of COM L5PNs, combined with 1A-mediated inhibition of CPn and COM-biphasic L5PNs, may facilitate executive function by focusing network activity within cortical circuits subserving the most appropriate behavioral output. Frontiers Media S.A. 2014-08-26 /pmc/articles/PMC4144257/ /pubmed/25206322 http://dx.doi.org/10.3389/fncir.2014.00097 Text en Copyright © 2014 Stephens, Avesar and Gulledge. 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
Stephens, Emily K.
Avesar, Daniel
Gulledge, Allan T.
Activity-dependent serotonergic excitation of callosal projection neurons in the mouse prefrontal cortex
title Activity-dependent serotonergic excitation of callosal projection neurons in the mouse prefrontal cortex
title_full Activity-dependent serotonergic excitation of callosal projection neurons in the mouse prefrontal cortex
title_fullStr Activity-dependent serotonergic excitation of callosal projection neurons in the mouse prefrontal cortex
title_full_unstemmed Activity-dependent serotonergic excitation of callosal projection neurons in the mouse prefrontal cortex
title_short Activity-dependent serotonergic excitation of callosal projection neurons in the mouse prefrontal cortex
title_sort activity-dependent serotonergic excitation of callosal projection neurons in the mouse prefrontal cortex
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4144257/
https://www.ncbi.nlm.nih.gov/pubmed/25206322
http://dx.doi.org/10.3389/fncir.2014.00097
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