Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, Victoria, Australia.
Department Medicine and Radiology, University of Melbourne, St Vincent's Hospital, Fitzroy, Victoria, Australia.
Br J Pharmacol. 2024 Jul;181(14):2270-2286. doi: 10.1111/bph.16099. Epub 2023 Jun 16.
Heart failure remains a leading cause of morbidity and mortality worldwide. Current treatment for patients with heart failure include drugs targeting G protein-coupled receptors such as β-adrenoceptor antagonists (β-blockers) and angiotensin II type 1 receptor antagonists (or angiotensin II receptor blockers). However, many patients progress to advanced heart failure with persistent symptoms, despite treatment with available therapeutics that have been shown to reduce mortality and mortality. GPCR targets currently being explored for the development of novel heart failure therapeutics include adenosine receptor, formyl peptide receptor, relaxin/insulin-like family peptide receptor, vasopressin receptor, endothelin receptor and the glucagon-like peptide 1 receptor. Many GPCR drug candidates are limited by insufficient efficacy and/or dose-limiting unwanted effects. Understanding the current challenges hindering successful clinical translation and the potential to overcome existing limitations will facilitate the future development of novel heart failure therapeutics. LINKED ARTICLES: This article is part of a themed issue Therapeutic Targeting of G Protein-Coupled Receptors: hot topics from the Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists 2021 Virtual Annual Scientific Meeting. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v181.14/issuetoc.
心力衰竭仍然是全球发病率和死亡率的主要原因。目前心力衰竭患者的治疗包括针对 G 蛋白偶联受体的药物,如β-肾上腺素受体拮抗剂(β-受体阻滞剂)和血管紧张素 II 型 1 型受体拮抗剂(或血管紧张素 II 受体阻滞剂)。然而,许多患者尽管接受了已证明可降低死亡率的现有治疗方法治疗,但仍进展为持续存在症状的晚期心力衰竭。目前正在探索用于开发新型心力衰竭治疗药物的 GPCR 靶点包括腺苷受体、甲酰肽受体、松弛素/胰岛素样家族肽受体、血管加压素受体、内皮素受体和胰高血糖素样肽 1 受体。许多 GPCR 药物候选物受到疗效不足和/或剂量限制的不良作用的限制。了解阻碍成功临床转化的当前挑战以及克服现有局限性的潜力,将有助于新型心力衰竭治疗药物的未来发展。
本文是 2021 年澳大利亚临床和实验药理学和毒理学协会虚拟年会治疗性靶向 G 蛋白偶联受体专题的一部分。要查看本节中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v181.14/issuetoc.