β-blockers are prescribed for a variety of cardiovascular conditions including hypertension, heart failure, primary treatment of myocardial infarction (MI), and secondary prevention of ischemic cardiac events. Yet they remain underprescribed in populations at increased risk for cardiovascular disease because of tolerability and safety concerns. β-Blockers are heterogeneous with respect to pharmacokinetic and pharmacodynamic effects. "Original" agents were nonselective, blocking both β1-adrenoceptors and β2- adrenoceptors. Later, new agents were developed with selectivity for β1-adrenoceptors, and were subsequently followed by β-blockers, which exhibit additional effects, such as vasodilation. Among newer agents, labetalol, carvedilol, and nebivolol have been approved for use in the United States. Nebivolol possesses both β1-selectivity and nitric oxide-mediated vasodilatory effects, while carvedilol has attractive effects on insulin resistance and exhibits antioxidant effects. Newer β-blockers may overcome concerns about efficacy, adverse effects, and tolerability, while delivering cardiovascular protection. © 2009 Wiley Periodicals, Inc.
CITATION STYLE
Manrique, C., Giles, T. D., Ferdinand, K. C., & Sowers, J. R. (2009). Realities of newer β-blockers for the management of hypertension. Journal of Clinical Hypertension. Blackwell Publishing Inc. https://doi.org/10.1111/j.1751-7176.2009.00140.x
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