Pretreatment of sildenafil attenuates ischemia-reperfusion renal injury in rats

Am J Physiol Renal Physiol. 2009 Aug;297(2):F362-70. doi: 10.1152/ajprenal.90609.2008. Epub 2009 May 27.

Abstract

Sildenafil was the first selective inhibitor of phosphodiesterase-5 (PDE5) to be widely used for treating erectile dysfunction. Many recent studies have investigated the cardioprotective role of sildenafil in animal models. We evaluated the protective effects of sildenafil in experimental renal ischemia-reperfusion (IR) injury in two studies. In study 1, male Sprague-Dawley rats were divided into four groups: sham, sildenafil-treated sham, vehicle-treated IR, and sildenafil-treated IR groups. In study 2, we divided the rats into two groups: sildenafil-treated IR rats and PD98059 (ERK inhibitor)+sildenafil-treated IR rats. Functional parameters of the kidney were evaluated at the molecular and structural levels. Blood urea nitrogen (BUN) and serum creatinine levels were lower in sildenafil-treated IR rats than in vehicle-treated IR rats. The expression of inducible (iNOS) and endothelial nitric oxide synthase (eNOS) proteins in sildenafil-treated IR rats was significantly higher than in vehicle-treated IR rats. Pretreatment with sildenafil in IR rats increased ERK phosphorylation and reduced the renal Bax/Bcl-2 ratio, renal caspase-3 activity, and terminal dUTP nick end-labeling-positive apoptotic cells. In contrast, PD98059 treatment increased BUN and serum creatinine levels and attenuated the sildenafil-induced expression of pERK, iNOS, eNOS, and Bcl-2. PD98059 also increased caspase-3 activity but did not decrease the sildenafil-induced accumulation of cGMP. In conclusion, this study suggests that sildenafil has antiapoptotic effects in experimental IR renal injury via ERK phosphorylation, induction of iNOS and eNOS production, and a decrease in the Bax/Bcl-2 ratio.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Blood Urea Nitrogen
  • Caspase 3 / metabolism
  • Creatinine / blood
  • Cyclic GMP / metabolism
  • Cyclic Nucleotide Phosphodiesterases, Type 5 / metabolism
  • Disease Models, Animal
  • Drug Administration Schedule
  • Extracellular Signal-Regulated MAP Kinases / antagonists & inhibitors
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Flavonoids / administration & dosage
  • Kidney Diseases / enzymology
  • Kidney Diseases / pathology
  • Kidney Diseases / prevention & control*
  • Male
  • Nitric Oxide Synthase Type II / metabolism
  • Nitric Oxide Synthase Type III / metabolism
  • Phosphodiesterase 5 Inhibitors*
  • Phosphodiesterase Inhibitors / administration & dosage*
  • Phosphorylation
  • Piperazines / administration & dosage*
  • Protein Kinase Inhibitors / administration & dosage
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Purines / administration & dosage
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion Injury / enzymology
  • Reperfusion Injury / pathology
  • Reperfusion Injury / prevention & control*
  • Sildenafil Citrate
  • Sulfones / administration & dosage*
  • Time Factors
  • bcl-2-Associated X Protein / metabolism

Substances

  • Bax protein, rat
  • Flavonoids
  • Phosphodiesterase 5 Inhibitors
  • Phosphodiesterase Inhibitors
  • Piperazines
  • Protein Kinase Inhibitors
  • Proto-Oncogene Proteins c-bcl-2
  • Purines
  • Sulfones
  • bcl-2-Associated X Protein
  • Creatinine
  • Sildenafil Citrate
  • Nitric Oxide Synthase Type II
  • Nitric Oxide Synthase Type III
  • Nos2 protein, rat
  • Nos3 protein, rat
  • Extracellular Signal-Regulated MAP Kinases
  • Cyclic Nucleotide Phosphodiesterases, Type 5
  • Casp3 protein, rat
  • Caspase 3
  • Cyclic GMP
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one