Abstract
β-adrenergic signaling is an important regulator of myocardial function. During the progression of heart failure (HF), a reproducible series of biochemical events occurs that affects β-adrenergic receptor (β-AR) signaling and cardiac function. Furthermore, there are pathophysiologic alterations in the expression and regulation of proteins that are regulated by β-ARs during HF. Analyses of these complex signaling pathways have led to a better understanding of HF mechanisms and the use of β-adrenergic antagonists, which have notably altered HF-related morbidity and mortality. Despite therapeutic advances that have affected β-AR signaling, HF remains a leading cause of hospitalization and a principal cause of death in industrialized nations. In this review, we summarize current insights into β-adrenergic signal-transduction pathways, the best-described β-AR polymorphisms, and therapies that target the β-AR pathway in HF.
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David Feldman has worked as a consultant for GlaxoSmithKline, Medtronic, SCIOS and Abbott. Michael Bristow has acted as a consultant for Astra Zeneca, Guidant, Mylan, Paracor, CVRx, Inspiration Medical, Cardiac Dimensions and Novartis; as an equity officer or director for Myogen and ARCA Discovery; and has received research support from Astra Zeneca, Guidant, Myogen, ARCA and Mylan.
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Feldman, D., Carnes, C., Abraham, W. et al. Mechanisms of Disease: β-adrenergic receptors—alterations in signal transduction and pharmacogenomics in heart failure. Nat Rev Cardiol 2, 475–483 (2005). https://doi.org/10.1038/ncpcardio0309
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DOI: https://doi.org/10.1038/ncpcardio0309
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