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Tapping into 5-HT(3) Receptors to Modify Metabolic and Immune Responses
5-hydroxytryptamine type 3 (5-HT(3)) receptors are ligand gated ion channels, which clearly distinguish their mode of action from the other G-protein coupled 5-HT or serotonin receptors. 5-HT(3) receptors are well established targets for emesis and gastrointestinal mobility and are used as adjunct t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584345/ https://www.ncbi.nlm.nih.gov/pubmed/34769340 http://dx.doi.org/10.3390/ijms222111910 |
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author | Irving, Helen Turek, Ilona Kettle, Christine Yaakob, Nor |
author_facet | Irving, Helen Turek, Ilona Kettle, Christine Yaakob, Nor |
author_sort | Irving, Helen |
collection | PubMed |
description | 5-hydroxytryptamine type 3 (5-HT(3)) receptors are ligand gated ion channels, which clearly distinguish their mode of action from the other G-protein coupled 5-HT or serotonin receptors. 5-HT(3) receptors are well established targets for emesis and gastrointestinal mobility and are used as adjunct targets in treating schizophrenia. However, the distribution of these receptors is wider than the nervous system and there is potential that these additional sites can be targeted to modulate inflammatory and/or metabolic conditions. Recent progress in structural biology and pharmacology of 5-HT(3) receptors have provided profound insights into mechanisms of their action. These advances, combined with insights into clinical relevance of mutations in genes encoding 5-HT(3) subunits and increasing understanding of their implications in patient’s predisposition to diseases and response to the treatment, open new avenues for personalized precision medicine. In this review, we recap on the current status of 5-HT(3) receptor-based therapies using a biochemical and physiological perspective. We assess the potential for targeting 5-HT(3) receptors in conditions involving metabolic or inflammatory disorders based on recent findings, underscoring the challenges and limitations of this approach. |
format | Online Article Text |
id | pubmed-8584345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85843452021-11-12 Tapping into 5-HT(3) Receptors to Modify Metabolic and Immune Responses Irving, Helen Turek, Ilona Kettle, Christine Yaakob, Nor Int J Mol Sci Review 5-hydroxytryptamine type 3 (5-HT(3)) receptors are ligand gated ion channels, which clearly distinguish their mode of action from the other G-protein coupled 5-HT or serotonin receptors. 5-HT(3) receptors are well established targets for emesis and gastrointestinal mobility and are used as adjunct targets in treating schizophrenia. However, the distribution of these receptors is wider than the nervous system and there is potential that these additional sites can be targeted to modulate inflammatory and/or metabolic conditions. Recent progress in structural biology and pharmacology of 5-HT(3) receptors have provided profound insights into mechanisms of their action. These advances, combined with insights into clinical relevance of mutations in genes encoding 5-HT(3) subunits and increasing understanding of their implications in patient’s predisposition to diseases and response to the treatment, open new avenues for personalized precision medicine. In this review, we recap on the current status of 5-HT(3) receptor-based therapies using a biochemical and physiological perspective. We assess the potential for targeting 5-HT(3) receptors in conditions involving metabolic or inflammatory disorders based on recent findings, underscoring the challenges and limitations of this approach. MDPI 2021-11-02 /pmc/articles/PMC8584345/ /pubmed/34769340 http://dx.doi.org/10.3390/ijms222111910 Text en © 2021 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 | Review Irving, Helen Turek, Ilona Kettle, Christine Yaakob, Nor Tapping into 5-HT(3) Receptors to Modify Metabolic and Immune Responses |
title | Tapping into 5-HT(3) Receptors to Modify Metabolic and Immune Responses |
title_full | Tapping into 5-HT(3) Receptors to Modify Metabolic and Immune Responses |
title_fullStr | Tapping into 5-HT(3) Receptors to Modify Metabolic and Immune Responses |
title_full_unstemmed | Tapping into 5-HT(3) Receptors to Modify Metabolic and Immune Responses |
title_short | Tapping into 5-HT(3) Receptors to Modify Metabolic and Immune Responses |
title_sort | tapping into 5-ht(3) receptors to modify metabolic and immune responses |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584345/ https://www.ncbi.nlm.nih.gov/pubmed/34769340 http://dx.doi.org/10.3390/ijms222111910 |
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