Sildenafil promotes neuroprotection of the pelvic ganglia neurones after bilateral cavernosal nerve resection in the rat

BJU Int. 2013 Jan;111(1):159-70. doi: 10.1111/j.1464-410X.2012.11278.x. Epub 2012 Jun 6.

Abstract

Objective: To determine the gene expression profile of pelvic ganglia neurones after bilateral cavernosal nerve resection (BCNR) and subsequent treatment with sildenafil in relation to neurotrophic-related pathways.

Materials and methods: Fisher rats aged 5 months were subjected to BCNR or sham operation and treated with or without sildenafil (20 mg/kg body-weight in drinking water) for 7 days. Total RNA isolated from pelvic ganglia was subjected to reverse transcription and then to quantitative reverse transcriptase-polymerase chain reaction (PCR) with the RAT-neurotrophic array. Results were corroborated by real-time PCR and western blotting. Another set of animals were injected with a fluorescent tracer at the base of the penis, 7 days before BCNR or sham operation, and were sacrificed 7 days after surgery. Sections of pelvic ganglia were used for immunohistochemistry with antibodies against neurturin, neuronal nitric oxide synthase, tyrosine hydroxylase and glial cell line-derived neurotrophic factor receptor α2.

Results: A down-regulation of the expression of neuronal nitric oxide synthase accompanied by changes in the level of cholinergic neurotrophic factors, such as neurturin and its receptor glial cell line-derived neurotrophic factor receptor α2, artemin, neurotrophin-4 and cilliary neurotrophic factor, was observed 7 days after BCNR in pelvic ganglia neurones. Treatment with sildenafil, starting immediately after surgery, reversed all these changes at a level similar to that in sham-operated animals.

Conclusions: Sildenafil treatment promotes changes in the neurotrophic phenotype, leading to a regenerative state of pelvic ganglia neurones. The present study provides a justification for the use of phosphodiesterase 5 inhibitors as a neuroprotective agent after BCNR.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Ganglia, Autonomic / drug effects*
  • Ganglia, Autonomic / metabolism
  • Gene Expression / drug effects
  • Glial Cell Line-Derived Neurotrophic Factor Receptors / genetics*
  • Glial Cell Line-Derived Neurotrophic Factor Receptors / metabolism
  • Male
  • Neurons / metabolism
  • Neuroprotective Agents / pharmacology*
  • Neurturin / metabolism
  • Nitric Oxide Synthase Type I / metabolism
  • Organ Sparing Treatments / methods
  • Pelvis / innervation
  • Penis / drug effects
  • Penis / innervation*
  • Penis / surgery
  • Phosphodiesterase 5 Inhibitors / pharmacology*
  • Piperazines / pharmacology*
  • Purines / pharmacology
  • Rats
  • Rats, Inbred F344
  • Rats, Sprague-Dawley
  • Signal Transduction / drug effects
  • Sildenafil Citrate
  • Sulfones / pharmacology*

Substances

  • Glial Cell Line-Derived Neurotrophic Factor Receptors
  • Neuroprotective Agents
  • Neurturin
  • Phosphodiesterase 5 Inhibitors
  • Piperazines
  • Purines
  • Sulfones
  • Sildenafil Citrate
  • Nitric Oxide Synthase Type I