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G Protein–Coupled Receptors in Asthma Therapy: Pharmacology and Drug Action

Asthma is a heterogeneous inflammatory disease of the airways that is associated with airway hyperresponsiveness and airflow limitation. Although asthma was once simply categorized as atopic or nonatopic, emerging analyses over the last few decades have revealed a variety of asthma endotypes that ar...

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Autores principales: Wendell, Stacy Gelhaus, Fan, Hao, Zhang, Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Pharmacology and Experimental Therapeutics 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878000/
https://www.ncbi.nlm.nih.gov/pubmed/31767622
http://dx.doi.org/10.1124/pr.118.016899
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author Wendell, Stacy Gelhaus
Fan, Hao
Zhang, Cheng
author_facet Wendell, Stacy Gelhaus
Fan, Hao
Zhang, Cheng
author_sort Wendell, Stacy Gelhaus
collection PubMed
description Asthma is a heterogeneous inflammatory disease of the airways that is associated with airway hyperresponsiveness and airflow limitation. Although asthma was once simply categorized as atopic or nonatopic, emerging analyses over the last few decades have revealed a variety of asthma endotypes that are attributed to numerous pathophysiological mechanisms. The classification of asthma by endotype is primarily routed in different profiles of airway inflammation that contribute to bronchoconstriction. Many asthma therapeutics target G protein–coupled receptors (GPCRs), which either enhance bronchodilation or prevent bronchoconstriction. Short-acting and long-acting β(2)-agonists are widely used bronchodilators that signal through the activation of the β(2)-adrenergic receptor. Short-acting and long-acting antagonists of muscarinic acetylcholine receptors are used to reduce bronchoconstriction by blocking the action of acetylcholine. Leukotriene antagonists that block the signaling of cysteinyl leukotriene receptor 1 are used as an add-on therapy to reduce bronchoconstriction and inflammation induced by cysteinyl leukotrienes. A number of GPCR-targeting asthma drug candidates are also in different stages of development. Among them, antagonists of prostaglandin D(2) receptor 2 have advanced into phase III clinical trials. Others, including antagonists of the adenosine A(2B) receptor and the histamine H4 receptor, are in early stages of clinical investigation. In the past decade, significant research advancements in pharmacology, cell biology, structural biology, and molecular physiology have greatly deepened our understanding of the therapeutic roles of GPCRs in asthma and drug action on these GPCRs. This review summarizes our current understanding of GPCR signaling and pharmacology in the context of asthma treatment. SIGNIFICANCE STATEMENT: Although current treatment methods for asthma are effective for a majority of asthma patients, there are still a large number of patients with poorly controlled asthma who may experience asthma exacerbations. This review summarizes current asthma treatment methods and our understanding of signaling and pharmacology of G protein–coupled receptors (GPCRs) in asthma therapy, and discusses controversies regarding the use of GPCR drugs and new opportunities in developing GPCR-targeting therapeutics for the treatment of asthma.
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spelling pubmed-68780002020-02-04 G Protein–Coupled Receptors in Asthma Therapy: Pharmacology and Drug Action Wendell, Stacy Gelhaus Fan, Hao Zhang, Cheng Pharmacol Rev Review Article Asthma is a heterogeneous inflammatory disease of the airways that is associated with airway hyperresponsiveness and airflow limitation. Although asthma was once simply categorized as atopic or nonatopic, emerging analyses over the last few decades have revealed a variety of asthma endotypes that are attributed to numerous pathophysiological mechanisms. The classification of asthma by endotype is primarily routed in different profiles of airway inflammation that contribute to bronchoconstriction. Many asthma therapeutics target G protein–coupled receptors (GPCRs), which either enhance bronchodilation or prevent bronchoconstriction. Short-acting and long-acting β(2)-agonists are widely used bronchodilators that signal through the activation of the β(2)-adrenergic receptor. Short-acting and long-acting antagonists of muscarinic acetylcholine receptors are used to reduce bronchoconstriction by blocking the action of acetylcholine. Leukotriene antagonists that block the signaling of cysteinyl leukotriene receptor 1 are used as an add-on therapy to reduce bronchoconstriction and inflammation induced by cysteinyl leukotrienes. A number of GPCR-targeting asthma drug candidates are also in different stages of development. Among them, antagonists of prostaglandin D(2) receptor 2 have advanced into phase III clinical trials. Others, including antagonists of the adenosine A(2B) receptor and the histamine H4 receptor, are in early stages of clinical investigation. In the past decade, significant research advancements in pharmacology, cell biology, structural biology, and molecular physiology have greatly deepened our understanding of the therapeutic roles of GPCRs in asthma and drug action on these GPCRs. This review summarizes our current understanding of GPCR signaling and pharmacology in the context of asthma treatment. SIGNIFICANCE STATEMENT: Although current treatment methods for asthma are effective for a majority of asthma patients, there are still a large number of patients with poorly controlled asthma who may experience asthma exacerbations. This review summarizes current asthma treatment methods and our understanding of signaling and pharmacology of G protein–coupled receptors (GPCRs) in asthma therapy, and discusses controversies regarding the use of GPCR drugs and new opportunities in developing GPCR-targeting therapeutics for the treatment of asthma. The American Society for Pharmacology and Experimental Therapeutics 2020-01 2020-01 /pmc/articles/PMC6878000/ /pubmed/31767622 http://dx.doi.org/10.1124/pr.118.016899 Text en Copyright © 2019 by The Author(s) http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the CC BY-NC Attribution 4.0 International license (http://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Review Article
Wendell, Stacy Gelhaus
Fan, Hao
Zhang, Cheng
G Protein–Coupled Receptors in Asthma Therapy: Pharmacology and Drug Action
title G Protein–Coupled Receptors in Asthma Therapy: Pharmacology and Drug Action
title_full G Protein–Coupled Receptors in Asthma Therapy: Pharmacology and Drug Action
title_fullStr G Protein–Coupled Receptors in Asthma Therapy: Pharmacology and Drug Action
title_full_unstemmed G Protein–Coupled Receptors in Asthma Therapy: Pharmacology and Drug Action
title_short G Protein–Coupled Receptors in Asthma Therapy: Pharmacology and Drug Action
title_sort g protein–coupled receptors in asthma therapy: pharmacology and drug action
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6878000/
https://www.ncbi.nlm.nih.gov/pubmed/31767622
http://dx.doi.org/10.1124/pr.118.016899
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