Beta blockers, nitric oxide, and cardiovascular disease

Curr Opin Pharmacol. 2013 Apr;13(2):265-73. doi: 10.1016/j.coph.2012.12.002. Epub 2013 Jan 5.

Abstract

The third generation β-blockers possess important ancillary properties besides inhibiting β-adrenoceptors. Among them, nebivolol activates nitric oxide synthase (NOS). Nebivolol and carvedilol preserve NOS activity by reducing asymmetrical dimethylarginine (AMDA) and enhance the bioavailability of nitric oxide (NO) because of their antioxidant properties. Concerning the treatment of hypertension and chronic heart failure, these third generation β-blockers show distinct advantages resulting from their NO-dependent effects (vasodilatation, anti-proliferation and cardioprotection), which may translate into a more effective clinical outcome than that obtained with the conventional β-blockers. Impaired NOS activity and reduced NO bioavailability are common initiators of cardiovascular dysfunction. Thus, owing to their NO-mediated actions, the new generation β-blockers should find more clinical applications in the treatment of cardiovascular diseases.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adrenergic beta-Antagonists / pharmacology*
  • Adrenergic beta-Antagonists / therapeutic use
  • Animals
  • Antioxidants / pharmacology*
  • Antioxidants / therapeutic use
  • Arginine / analogs & derivatives
  • Arginine / physiology
  • Cardiovascular Diseases / drug therapy
  • Cardiovascular Diseases / metabolism*
  • Cardiovascular Diseases / physiopathology
  • Humans
  • Nitric Oxide / physiology*
  • Vasodilation / physiology

Substances

  • Adrenergic beta-Antagonists
  • Antioxidants
  • Nitric Oxide
  • N,N-dimethylarginine
  • Arginine