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On the G Protein-Coupled Receptor Neuromodulation of the Claustrum

G protein-coupled receptors modulate the synaptic glutamate and GABA transmission of the claustrum. The work focused on the transmitter–receptor relationships in the claustral catecholamine system and receptor–receptor interactions between kappa opioid receptors (KOR) and SomatostatinR2 (SSTR2) in c...

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Autores principales: Borroto-Escuela, Dasiel O., Fuxe, Kjell
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942600/
https://www.ncbi.nlm.nih.gov/pubmed/31172348
http://dx.doi.org/10.1007/s11064-019-02822-4
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author Borroto-Escuela, Dasiel O.
Fuxe, Kjell
author_facet Borroto-Escuela, Dasiel O.
Fuxe, Kjell
author_sort Borroto-Escuela, Dasiel O.
collection PubMed
description G protein-coupled receptors modulate the synaptic glutamate and GABA transmission of the claustrum. The work focused on the transmitter–receptor relationships in the claustral catecholamine system and receptor–receptor interactions between kappa opioid receptors (KOR) and SomatostatinR2 (SSTR2) in claustrum. Methods used involved immunohistochemistry and in situ proximity ligation assay (PLA) using confocal microscopy. Double immunolabeling studies on dopamine (DA) D1 receptor (D1R) and tyrosine hydroxylase (TH) immunoreactivities (IR) demonstrated that D1R IR existed in almost all claustral and dorsal endopiriform nucleus (DEn) nerve cell bodies, known as glutamate projection neurons, and D4R IR in large numbers of nerve cell bodies of the claustrum and DEn. However, only a low to moderate density of TH IR nerve terminals was observed in the DEn versus de few scattered TH IR terminals found in the claustrum. These results indicated that DA D1R and D4R transmission in the rat operated via long distance DA volume transmission in the rat claustrum and DEn to modulate claustral-sensory cortical glutamate transmission. Large numbers of these glutamate projection neurons also expressed KOR and SSTR2 which formed KOR-SSTR2 heteroreceptor complexes using PLA. Such receptor–receptor interactions can finetune the activity of the glutamate claustral-sensory cortex projections from inhibition to enhancement of their sensory cortex signaling. This can give the sensory cortical regions significant help in deciding on the salience to be given to various incoming sensory stimuli.
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spelling pubmed-69426002020-01-16 On the G Protein-Coupled Receptor Neuromodulation of the Claustrum Borroto-Escuela, Dasiel O. Fuxe, Kjell Neurochem Res Original Paper G protein-coupled receptors modulate the synaptic glutamate and GABA transmission of the claustrum. The work focused on the transmitter–receptor relationships in the claustral catecholamine system and receptor–receptor interactions between kappa opioid receptors (KOR) and SomatostatinR2 (SSTR2) in claustrum. Methods used involved immunohistochemistry and in situ proximity ligation assay (PLA) using confocal microscopy. Double immunolabeling studies on dopamine (DA) D1 receptor (D1R) and tyrosine hydroxylase (TH) immunoreactivities (IR) demonstrated that D1R IR existed in almost all claustral and dorsal endopiriform nucleus (DEn) nerve cell bodies, known as glutamate projection neurons, and D4R IR in large numbers of nerve cell bodies of the claustrum and DEn. However, only a low to moderate density of TH IR nerve terminals was observed in the DEn versus de few scattered TH IR terminals found in the claustrum. These results indicated that DA D1R and D4R transmission in the rat operated via long distance DA volume transmission in the rat claustrum and DEn to modulate claustral-sensory cortical glutamate transmission. Large numbers of these glutamate projection neurons also expressed KOR and SSTR2 which formed KOR-SSTR2 heteroreceptor complexes using PLA. Such receptor–receptor interactions can finetune the activity of the glutamate claustral-sensory cortex projections from inhibition to enhancement of their sensory cortex signaling. This can give the sensory cortical regions significant help in deciding on the salience to be given to various incoming sensory stimuli. Springer US 2019-06-06 2020 /pmc/articles/PMC6942600/ /pubmed/31172348 http://dx.doi.org/10.1007/s11064-019-02822-4 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Borroto-Escuela, Dasiel O.
Fuxe, Kjell
On the G Protein-Coupled Receptor Neuromodulation of the Claustrum
title On the G Protein-Coupled Receptor Neuromodulation of the Claustrum
title_full On the G Protein-Coupled Receptor Neuromodulation of the Claustrum
title_fullStr On the G Protein-Coupled Receptor Neuromodulation of the Claustrum
title_full_unstemmed On the G Protein-Coupled Receptor Neuromodulation of the Claustrum
title_short On the G Protein-Coupled Receptor Neuromodulation of the Claustrum
title_sort on the g protein-coupled receptor neuromodulation of the claustrum
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942600/
https://www.ncbi.nlm.nih.gov/pubmed/31172348
http://dx.doi.org/10.1007/s11064-019-02822-4
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