Preclinical evidence that sildenafil and vardenafil activate chloride transport in cystic fibrosis

Am J Respir Crit Care Med. 2008 Mar 1;177(5):506-15. doi: 10.1164/rccm.200703-344OC. Epub 2007 Nov 15.


Rationale: Sildenafil has been implicated in the activation of cystic fibrosis transmembrane conductance regulator (CFTR) protein. The effect was observed in vitro and in the presence of doses roughly 300 times larger than those commonly used for treating erectile dysfunction.

Objectives: To evaluate in vivo the therapeutic efficacy of clinical doses of sildenafil and vardenafil, two clinically approved phosphodiesterase 5 inhibitors, for activating ion transport in cystic fibrosis.

Methods: We used transepithelial potential difference in vivo across the nasal mucosa as a measure of sodium and chloride transport. The effect of a single intraperitoneal injection of sildenafil (0.7 mg/kg) or vardenafil (0.14 mg/kg) was investigated in F508del, cftr knockout and normal homozygous mice.

Measurements and main results: In F508del mice, but not in cftr knockout mice, the chloride conductance, evaluated by perfusing the nasal mucosa with a chloride-free solution in the presence of amiloride and with forskolin, was corrected 1 hour after sildenafil administration. A more prolonged effect, persisting for at least 24 hours, was observed with vardenafil. The forskolin response was increased after sildenafil and vardenafil in both normal and F508del mutant animals. In F508del mice, the chloride conductance in the presence of 200 microM 4-4'-diisothiocyanostilbene-2,2'-disulphonic acid, an inhibitor of alternative chloride channels, was much higher after sildenafil injection than after placebo treatment. No effect on the sodium conductance was detected in any group of animals.

Conclusions: Our results provide preclinical evidence that both drugs stimulate chloride transport activity of F508del-CFTR protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chlorides / metabolism*
  • Colforsin / metabolism
  • Cystic Fibrosis / metabolism*
  • Cystic Fibrosis Transmembrane Conductance Regulator / metabolism
  • Disease Models, Animal
  • Imidazoles / administration & dosage
  • Imidazoles / pharmacokinetics*
  • Injections, Intraperitoneal
  • Ion Transport / drug effects*
  • Membrane Potentials / drug effects*
  • Mice
  • Mice, Inbred CFTR
  • Nasal Mucosa / metabolism
  • Phosphodiesterase 5 Inhibitors*
  • Phosphodiesterase Inhibitors / administration & dosage
  • Phosphodiesterase Inhibitors / pharmacokinetics*
  • Phosphodiesterase Inhibitors / pharmacology*
  • Piperazines / administration & dosage
  • Piperazines / pharmacokinetics*
  • Protein Modification, Translational
  • Purines / administration & dosage
  • Purines / pharmacokinetics
  • Sildenafil Citrate
  • Sulfones / administration & dosage
  • Sulfones / pharmacokinetics*
  • Triazines / administration & dosage
  • Triazines / pharmacokinetics
  • Vardenafil Dihydrochloride


  • Chlorides
  • Imidazoles
  • Phosphodiesterase 5 Inhibitors
  • Phosphodiesterase Inhibitors
  • Piperazines
  • Purines
  • Sulfones
  • Triazines
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Colforsin
  • Vardenafil Dihydrochloride
  • Sildenafil Citrate