Literature DB >> 31767622

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

Stacy Gelhaus Wendell1, Hao Fan2, Cheng Zhang3.   

Abstract

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 D2 receptor 2 have advanced into phase III clinical trials. Others, including antagonists of the adenosine A2B 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.
Copyright © 2019 by The Author(s).

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Year:  2020        PMID: 31767622      PMCID: PMC6878000          DOI: 10.1124/pr.118.016899

Source DB:  PubMed          Journal:  Pharmacol Rev        ISSN: 0031-6997            Impact factor:   25.468


  687 in total

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Journal:  Curr Pharm Des       Date:  2006       Impact factor: 3.116

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10.  Mogamulizumab versus vorinostat in previously treated cutaneous T-cell lymphoma (MAVORIC): an international, open-label, randomised, controlled phase 3 trial.

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  17 in total

1.  Can GPCRs Be Targeted to Control Inflammation in Asthma?

Authors:  Pawan Sharma; Raymond B Penn
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

2.  The role of EP2 receptors in mediating the ultra-long-lasting intraocular pressure reduction by JV-GL1.

Authors:  Jacques A Bertrand; David F Woodward; Joseph M Sherwood; Jenny W Wang; Darryl R Overby
Journal:  Br J Ophthalmol       Date:  2020-11-25       Impact factor: 4.638

3.  β2 -Adrenoceptor agonist profiling reveals biased signalling phenotypes for the β2 -adrenoceptor with possible implications for the treatment of asthma.

Authors:  Francesco De Pascali; Michael Ippolito; Emily Wolfe; Konstantin E Komolov; Nathan Hopfinger; Douglas Lemenze; Nicholas Kim; Roger S Armen; Steven S An; Charles P Scott; Jeffrey L Benovic
Journal:  Br J Pharmacol       Date:  2022-07-19       Impact factor: 9.473

4.  S-nitrosylation is required for β2AR desensitization and experimental asthma.

Authors:  Fabio V Fonseca; Thomas M Raffay; Kunhong Xiao; Precious J McLaughlin; Zhaoxia Qian; Zachary W Grimmett; Naoko Adachi; Benlian Wang; Alfred Hausladen; Brian A Cobb; Rongli Zhang; Douglas T Hess; Benjamin Gaston; Nevin A Lambert; James D Reynolds; Richard T Premont; Jonathan S Stamler
Journal:  Mol Cell       Date:  2022-08-04       Impact factor: 19.328

5.  International Union of Basic and Clinical Pharmacology. CIX. Differences and Similarities between Human and Rodent Prostaglandin E2 Receptors (EP1-4) and Prostacyclin Receptor (IP): Specific Roles in Pathophysiologic Conditions.

Authors:  Xavier Norel; Yukihiko Sugimoto; Gulsev Ozen; Heba Abdelazeem; Yasmine Amgoud; Amel Bouhadoun; Wesam Bassiouni; Marie Goepp; Salma Mani; Hasanga D Manikpurage; Amira Senbel; Dan Longrois; Akos Heinemann; Chengcan Yao; Lucie H Clapp
Journal:  Pharmacol Rev       Date:  2020-10       Impact factor: 25.468

Review 6.  Class C GPCRs in the airway.

Authors:  Brijeshkumar S Patel; Jovanka Ravix; Christina Pabelick; Y S Prakash
Journal:  Curr Opin Pharmacol       Date:  2020-05-04       Impact factor: 5.547

7.  Bitter Taste Receptors in the Airway Cells Functions.

Authors:  Pawan Sharma; Stanley Conaway; Deepak Deshpande
Journal:  Handb Exp Pharmacol       Date:  2022

Review 8.  RGS proteins, GRKs, and beta-arrestins modulate G protein-mediated signaling pathways in asthma.

Authors:  Nathalie Fuentes; Morgan McCullough; Reynold A Panettieri; Kirk M Druey
Journal:  Pharmacol Ther       Date:  2021-02-15       Impact factor: 13.400

Review 9.  Structural Insights into Ligand-Receptor Interactions Involved in Biased Agonism of G-Protein Coupled Receptors.

Authors:  Krzysztof Jóźwiak; Anita Płazińska
Journal:  Molecules       Date:  2021-02-06       Impact factor: 4.411

Review 10.  The Biology of Prostaglandins and Their Role as a Target for Allergic Airway Disease Therapy.

Authors:  Kijeong Lee; Sang Hag Lee; Tae Hoon Kim
Journal:  Int J Mol Sci       Date:  2020-03-08       Impact factor: 5.923

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