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Adenosine Receptors as Potential Therapeutic Analgesic Targets

Pain represents an international burden and a major socio-economic public health problem. New findings, detailed in this review, suggest that adenosine plays a significant role in neuropathic and inflammatory pain, by acting on its metabotropic adenosine receptors (A(1)AR, A(2A)AR, A(2B)AR, A(3)AR)....

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Autores principales: Haddad, Mansour, Cherchi, Federica, Alsalem, Mohammad, Al-saraireh, Yousef M., Madae’en, Saba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487796/
https://www.ncbi.nlm.nih.gov/pubmed/37685963
http://dx.doi.org/10.3390/ijms241713160
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author Haddad, Mansour
Cherchi, Federica
Alsalem, Mohammad
Al-saraireh, Yousef M.
Madae’en, Saba
author_facet Haddad, Mansour
Cherchi, Federica
Alsalem, Mohammad
Al-saraireh, Yousef M.
Madae’en, Saba
author_sort Haddad, Mansour
collection PubMed
description Pain represents an international burden and a major socio-economic public health problem. New findings, detailed in this review, suggest that adenosine plays a significant role in neuropathic and inflammatory pain, by acting on its metabotropic adenosine receptors (A(1)AR, A(2A)AR, A(2B)AR, A(3)AR). Adenosine receptor ligands have a practical translational potential based on the favorable efficacy and safety profiles that emerged from clinical research on various agonists and antagonists for different pathologies. The present review collects the latest studies on selected adenosine receptor ligands in different pain models. Here, we also covered the many hypothesized pathways and the role of newly synthesized allosteric adenosine receptor modulators. This review aims to present a summary of recent research on adenosine receptors as prospective therapeutic targets for a range of pain-related disorders.
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spelling pubmed-104877962023-09-09 Adenosine Receptors as Potential Therapeutic Analgesic Targets Haddad, Mansour Cherchi, Federica Alsalem, Mohammad Al-saraireh, Yousef M. Madae’en, Saba Int J Mol Sci Review Pain represents an international burden and a major socio-economic public health problem. New findings, detailed in this review, suggest that adenosine plays a significant role in neuropathic and inflammatory pain, by acting on its metabotropic adenosine receptors (A(1)AR, A(2A)AR, A(2B)AR, A(3)AR). Adenosine receptor ligands have a practical translational potential based on the favorable efficacy and safety profiles that emerged from clinical research on various agonists and antagonists for different pathologies. The present review collects the latest studies on selected adenosine receptor ligands in different pain models. Here, we also covered the many hypothesized pathways and the role of newly synthesized allosteric adenosine receptor modulators. This review aims to present a summary of recent research on adenosine receptors as prospective therapeutic targets for a range of pain-related disorders. MDPI 2023-08-24 /pmc/articles/PMC10487796/ /pubmed/37685963 http://dx.doi.org/10.3390/ijms241713160 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 Review
Haddad, Mansour
Cherchi, Federica
Alsalem, Mohammad
Al-saraireh, Yousef M.
Madae’en, Saba
Adenosine Receptors as Potential Therapeutic Analgesic Targets
title Adenosine Receptors as Potential Therapeutic Analgesic Targets
title_full Adenosine Receptors as Potential Therapeutic Analgesic Targets
title_fullStr Adenosine Receptors as Potential Therapeutic Analgesic Targets
title_full_unstemmed Adenosine Receptors as Potential Therapeutic Analgesic Targets
title_short Adenosine Receptors as Potential Therapeutic Analgesic Targets
title_sort adenosine receptors as potential therapeutic analgesic targets
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487796/
https://www.ncbi.nlm.nih.gov/pubmed/37685963
http://dx.doi.org/10.3390/ijms241713160
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