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The P2X1 receptor as a therapeutic target
Within the family of purinergic receptors, the P2X1 receptor is a ligand-gated ion channel that plays a role in urogenital, immune and cardiovascular function. Specifically, the P2X1 receptor has been implicated in controlling smooth muscle contractions of the vas deferens and therefore has emerged...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832217/ https://www.ncbi.nlm.nih.gov/pubmed/35821454 http://dx.doi.org/10.1007/s11302-022-09880-4 |
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author | Bennetts, Felix M. Mobbs, Jesse I. Ventura, Sabatino Thal, David M. |
author_facet | Bennetts, Felix M. Mobbs, Jesse I. Ventura, Sabatino Thal, David M. |
author_sort | Bennetts, Felix M. |
collection | PubMed |
description | Within the family of purinergic receptors, the P2X1 receptor is a ligand-gated ion channel that plays a role in urogenital, immune and cardiovascular function. Specifically, the P2X1 receptor has been implicated in controlling smooth muscle contractions of the vas deferens and therefore has emerged as an exciting drug target for male contraception. In addition, the P2X1 receptor contributes to smooth muscle contractions of the bladder and is a target to treat bladder dysfunction. Finally, platelets and neutrophils have populations of P2X1 receptors that could be targeted for thrombosis and inflammatory conditions. Drugs that specifically target the P2X1 receptor have been challenging to develop, and only recently have small molecule antagonists of the P2X1 receptor been available. However, these ligands need further biological validation for appropriate selectivity and drug-like properties before they will be suitable for use in preclinical models of disease. Although the atomic structure of the P2X1 receptor has yet to be determined, the recent discovery of several other P2X receptor structures and improvements in the field of structural biology suggests that this is now a distinct possibility. Such efforts may significantly improve drug discovery efforts at the P2X1 receptor. |
format | Online Article Text |
id | pubmed-9832217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-98322172023-01-12 The P2X1 receptor as a therapeutic target Bennetts, Felix M. Mobbs, Jesse I. Ventura, Sabatino Thal, David M. Purinergic Signal Review Article Within the family of purinergic receptors, the P2X1 receptor is a ligand-gated ion channel that plays a role in urogenital, immune and cardiovascular function. Specifically, the P2X1 receptor has been implicated in controlling smooth muscle contractions of the vas deferens and therefore has emerged as an exciting drug target for male contraception. In addition, the P2X1 receptor contributes to smooth muscle contractions of the bladder and is a target to treat bladder dysfunction. Finally, platelets and neutrophils have populations of P2X1 receptors that could be targeted for thrombosis and inflammatory conditions. Drugs that specifically target the P2X1 receptor have been challenging to develop, and only recently have small molecule antagonists of the P2X1 receptor been available. However, these ligands need further biological validation for appropriate selectivity and drug-like properties before they will be suitable for use in preclinical models of disease. Although the atomic structure of the P2X1 receptor has yet to be determined, the recent discovery of several other P2X receptor structures and improvements in the field of structural biology suggests that this is now a distinct possibility. Such efforts may significantly improve drug discovery efforts at the P2X1 receptor. Springer Netherlands 2022-07-11 2022-12 /pmc/articles/PMC9832217/ /pubmed/35821454 http://dx.doi.org/10.1007/s11302-022-09880-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Bennetts, Felix M. Mobbs, Jesse I. Ventura, Sabatino Thal, David M. The P2X1 receptor as a therapeutic target |
title | The P2X1 receptor as a therapeutic target |
title_full | The P2X1 receptor as a therapeutic target |
title_fullStr | The P2X1 receptor as a therapeutic target |
title_full_unstemmed | The P2X1 receptor as a therapeutic target |
title_short | The P2X1 receptor as a therapeutic target |
title_sort | p2x1 receptor as a therapeutic target |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832217/ https://www.ncbi.nlm.nih.gov/pubmed/35821454 http://dx.doi.org/10.1007/s11302-022-09880-4 |
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