Cargando…

5-HT6 Receptors Sex-Dependently Modulate Hippocampal Synaptic Activity through GABA Inhibition

The subtype 6 of the serotoninergic receptors (5-HT6Rs) is highly expressed in the hippocampus, and evidence indicates the beneficial effects of 5-HT6Rs blockade on short- and long-term memory in rodents. Nevertheless, the underlying functional mechanisms still need to be established. To this end, w...

Descripción completa

Detalles Bibliográficos
Autores principales: Lahogue, Caroline, Billard, Jean-Marie, Freret, Thomas, Bouet, Valentine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216834/
https://www.ncbi.nlm.nih.gov/pubmed/37238621
http://dx.doi.org/10.3390/biom13050751
_version_ 1785048392616902656
author Lahogue, Caroline
Billard, Jean-Marie
Freret, Thomas
Bouet, Valentine
author_facet Lahogue, Caroline
Billard, Jean-Marie
Freret, Thomas
Bouet, Valentine
author_sort Lahogue, Caroline
collection PubMed
description The subtype 6 of the serotoninergic receptors (5-HT6Rs) is highly expressed in the hippocampus, and evidence indicates the beneficial effects of 5-HT6Rs blockade on short- and long-term memory in rodents. Nevertheless, the underlying functional mechanisms still need to be established. To this end, we performed electrophysiological extracellular recordings to assess the effects of the 5-HT6Rs antagonist SB-271046 on the synaptic activity and functional plasticity at the CA3/CA1 hippocampal connections of male and female mice slices. We found that basal excitatory synaptic transmission and isolated N-methyl-D-aspartate receptors (NMDARs) activation were significantly increased by SB-271046. The NMDARs-related improvement was prevented by the GABAAR antagonist bicuculline in male but not in female mice. Regarding synaptic plasticity, neither paired-pulse facilitation (PPF) nor NMDARs-dependent long-term potentiation (LTP) (induced either by high-frequency or theta-burst stimulation) was affected by the 5-HT6Rs blockade. Taken together, our results indicate a sex-dependent 5-HT6Rs effect on synaptic activity at the CA3/CA1 hippocampal connections through changes in the excitation/inhibition balance.
format Online
Article
Text
id pubmed-10216834
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-102168342023-05-27 5-HT6 Receptors Sex-Dependently Modulate Hippocampal Synaptic Activity through GABA Inhibition Lahogue, Caroline Billard, Jean-Marie Freret, Thomas Bouet, Valentine Biomolecules Article The subtype 6 of the serotoninergic receptors (5-HT6Rs) is highly expressed in the hippocampus, and evidence indicates the beneficial effects of 5-HT6Rs blockade on short- and long-term memory in rodents. Nevertheless, the underlying functional mechanisms still need to be established. To this end, we performed electrophysiological extracellular recordings to assess the effects of the 5-HT6Rs antagonist SB-271046 on the synaptic activity and functional plasticity at the CA3/CA1 hippocampal connections of male and female mice slices. We found that basal excitatory synaptic transmission and isolated N-methyl-D-aspartate receptors (NMDARs) activation were significantly increased by SB-271046. The NMDARs-related improvement was prevented by the GABAAR antagonist bicuculline in male but not in female mice. Regarding synaptic plasticity, neither paired-pulse facilitation (PPF) nor NMDARs-dependent long-term potentiation (LTP) (induced either by high-frequency or theta-burst stimulation) was affected by the 5-HT6Rs blockade. Taken together, our results indicate a sex-dependent 5-HT6Rs effect on synaptic activity at the CA3/CA1 hippocampal connections through changes in the excitation/inhibition balance. MDPI 2023-04-26 /pmc/articles/PMC10216834/ /pubmed/37238621 http://dx.doi.org/10.3390/biom13050751 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lahogue, Caroline
Billard, Jean-Marie
Freret, Thomas
Bouet, Valentine
5-HT6 Receptors Sex-Dependently Modulate Hippocampal Synaptic Activity through GABA Inhibition
title 5-HT6 Receptors Sex-Dependently Modulate Hippocampal Synaptic Activity through GABA Inhibition
title_full 5-HT6 Receptors Sex-Dependently Modulate Hippocampal Synaptic Activity through GABA Inhibition
title_fullStr 5-HT6 Receptors Sex-Dependently Modulate Hippocampal Synaptic Activity through GABA Inhibition
title_full_unstemmed 5-HT6 Receptors Sex-Dependently Modulate Hippocampal Synaptic Activity through GABA Inhibition
title_short 5-HT6 Receptors Sex-Dependently Modulate Hippocampal Synaptic Activity through GABA Inhibition
title_sort 5-ht6 receptors sex-dependently modulate hippocampal synaptic activity through gaba inhibition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216834/
https://www.ncbi.nlm.nih.gov/pubmed/37238621
http://dx.doi.org/10.3390/biom13050751
work_keys_str_mv AT lahoguecaroline 5ht6receptorssexdependentlymodulatehippocampalsynapticactivitythroughgabainhibition
AT billardjeanmarie 5ht6receptorssexdependentlymodulatehippocampalsynapticactivitythroughgabainhibition
AT freretthomas 5ht6receptorssexdependentlymodulatehippocampalsynapticactivitythroughgabainhibition
AT bouetvalentine 5ht6receptorssexdependentlymodulatehippocampalsynapticactivitythroughgabainhibition