Targeting G Protein-Coupled Receptors for Heart Failure Treatment.
Bui San ThaiLing Yeong ChiaAnh T N NguyenChengxue Helena QinRebecca Helen RitchieDana Sabine HutchinsonAndrew R KompaPaul J WhiteLauren T MayPublished in: British journal of pharmacology (2023)
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 (GPCRs) such as 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 receptors, formyl peptide receptors, relaxin/insulin-like family peptide receptors, vasopressin receptors, endothelin receptors 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.
Keyphrases
- heart failure
- angiotensin ii
- angiotensin converting enzyme
- left ventricular
- atrial fibrillation
- vascular smooth muscle cells
- end stage renal disease
- acute heart failure
- small molecule
- type diabetes
- cardiac resynchronization therapy
- risk factors
- cardiovascular events
- metabolic syndrome
- cardiovascular disease
- depressive symptoms
- drug delivery
- skeletal muscle
- emergency department
- coronary artery disease
- human health
- insulin resistance