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Novel Therapeutic Targets for Migraine
Migraine, a primary headache disorder involving a dysfunctional trigeminal vascular system, remains a major debilitating neurological condition impacting many patients’ quality of life. Despite the success of multiple new migraine therapies, not all patients achieve significant clinical benefits. Th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9952984/ https://www.ncbi.nlm.nih.gov/pubmed/36831105 http://dx.doi.org/10.3390/biomedicines11020569 |
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author | Nisar, Areeba Ahmed, Zubair Yuan, Hsiangkuo |
author_facet | Nisar, Areeba Ahmed, Zubair Yuan, Hsiangkuo |
author_sort | Nisar, Areeba |
collection | PubMed |
description | Migraine, a primary headache disorder involving a dysfunctional trigeminal vascular system, remains a major debilitating neurological condition impacting many patients’ quality of life. Despite the success of multiple new migraine therapies, not all patients achieve significant clinical benefits. The success of CGRP pathway-targeted therapy highlights the importance of translating the mechanistic understanding toward effective therapy. Ongoing research has identified multiple potential mechanisms in migraine signaling and nociception. In this narrative review, we discuss several potential emerging therapeutic targets, including pituitary adenylate cyclase-activating polypeptide (PACAP), adenosine, δ-opioid receptor (DOR), potassium channels, transient receptor potential ion channels (TRP), and acid-sensing ion channels (ASIC). A better understanding of these mechanisms facilitates the discovery of novel therapeutic targets and provides more treatment options for improved clinical care. |
format | Online Article Text |
id | pubmed-9952984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99529842023-02-25 Novel Therapeutic Targets for Migraine Nisar, Areeba Ahmed, Zubair Yuan, Hsiangkuo Biomedicines Review Migraine, a primary headache disorder involving a dysfunctional trigeminal vascular system, remains a major debilitating neurological condition impacting many patients’ quality of life. Despite the success of multiple new migraine therapies, not all patients achieve significant clinical benefits. The success of CGRP pathway-targeted therapy highlights the importance of translating the mechanistic understanding toward effective therapy. Ongoing research has identified multiple potential mechanisms in migraine signaling and nociception. In this narrative review, we discuss several potential emerging therapeutic targets, including pituitary adenylate cyclase-activating polypeptide (PACAP), adenosine, δ-opioid receptor (DOR), potassium channels, transient receptor potential ion channels (TRP), and acid-sensing ion channels (ASIC). A better understanding of these mechanisms facilitates the discovery of novel therapeutic targets and provides more treatment options for improved clinical care. MDPI 2023-02-15 /pmc/articles/PMC9952984/ /pubmed/36831105 http://dx.doi.org/10.3390/biomedicines11020569 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 Nisar, Areeba Ahmed, Zubair Yuan, Hsiangkuo Novel Therapeutic Targets for Migraine |
title | Novel Therapeutic Targets for Migraine |
title_full | Novel Therapeutic Targets for Migraine |
title_fullStr | Novel Therapeutic Targets for Migraine |
title_full_unstemmed | Novel Therapeutic Targets for Migraine |
title_short | Novel Therapeutic Targets for Migraine |
title_sort | novel therapeutic targets for migraine |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9952984/ https://www.ncbi.nlm.nih.gov/pubmed/36831105 http://dx.doi.org/10.3390/biomedicines11020569 |
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