Sildenafil does not improve nitric oxide-mediated endothelium-dependent vascular responses in smokers

Br J Clin Pharmacol. 2004 Feb;57(2):209-12. doi: 10.1046/j.1365-2125.2003.01974.x.

Abstract

Aims: To examine the hypothesis that sildenafil, a phosphodiesterase type 5 inhibitor that inhibits cGMP breakdown, could enhance nitric oxide-mediated vasodilation and reverse endothelial dysfunction in chronic smokers.

Methods: Flow-mediated dilation of the brachial artery and forearm postischemic reactive hyperemia (both nitric oxide-mediated responses) were measured before and after sildenafil 50 mg and placebo in a double-blind, randomized, crossover study in 9 men who were chronic smokers (21 +/- 3 pack years).

Results: There was no significant change in flow-mediated dilation after either sildenafil (0.18%, 95%CI -1.7-2%) or placebo (0.24%, 95%CI -2.8-3.3%) (P = 0.88 and 0.8, respectively). Sildenafil had no significant effect on resting forearm blood flow or postischemic reactive hyperemia (P = 0.39 and 0.7, respectively). Resting heart rate and blood pressure were unaffected by sildenafil.

Conclusions: Acute sildenafil administration did not improve endothelial function in chronic smoking men.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Brachial Artery / drug effects
  • Cross-Over Studies
  • Double-Blind Method
  • Endothelium, Vascular / drug effects*
  • Humans
  • Male
  • Nitric Oxide / physiology*
  • Piperazines / pharmacology*
  • Purines
  • Sildenafil Citrate
  • Smoking / physiopathology*
  • Sulfones
  • Vasodilator Agents / pharmacology*

Substances

  • Piperazines
  • Purines
  • Sulfones
  • Vasodilator Agents
  • Nitric Oxide
  • Sildenafil Citrate