Pharmacology of nebivolol

J Pharm Belg. 1992 Jul-Aug;47(4):323-7.

Abstract

Nebivolol is a mixture of equal amounts of two enantiomers: SR3-nebivolol (d-nebivolol) and RS3-nebivolol (l-nebivolol). SR3-nebivolol is a potent and selective beta 1-adrenergic antagonist both in vitro and in vivo. Nebivolol acutely lowers blood pressure in spontaneously hypertensive rats and induces a slight decrease in total peripheral vascular resistance and a slight increase in cardiac output in anaesthetised dogs. These hemodynamics effects cannot be explained by beta 1-adrenergic antagonism and are largely attributable to RS3-nebivolol.

MeSH terms

  • Adrenergic beta-Antagonists / pharmacology*
  • Animals
  • Antihypertensive Agents / pharmacology
  • Benzopyrans / pharmacology*
  • Blood Pressure / drug effects
  • Cardiac Output / drug effects
  • Dogs
  • Ethanolamines / pharmacology*
  • Hemodynamics / drug effects*
  • Nebivolol
  • Rats
  • Rats, Inbred SHR
  • Receptors, Adrenergic, beta / drug effects
  • Vascular Resistance / drug effects

Substances

  • Adrenergic beta-Antagonists
  • Antihypertensive Agents
  • Benzopyrans
  • Ethanolamines
  • Receptors, Adrenergic, beta
  • Nebivolol