Resveratrol improves prostate fibrosis during progression of urinary dysfunction in chronic prostatitis

Environ Toxicol Pharmacol. 2017 Sep:54:120-124. doi: 10.1016/j.etap.2017.06.025. Epub 2017 Jul 1.

Abstract

Aim: We investigated whether prostate fibrosis was associated with urinary dysfunction in chronic prostatitis (CP) and whether resveratrol improved urinary dysfunction and the underlying molecular mechanism.

Methods: Rat model of CP was established via subcutaneous injections of DPT vaccine and subsequently treated with resveratrol. Bladder pressure and volume tests investigated the effect of resveratrol on urinary dysfunction in CP rats. Western blotting and immunohistochemical staining examined the expression level of C-kit/SCF and TGF-β/Wnt/β-catenin.

Results: Compared to the control group, the maximum capacity of the bladder, residual urine volume and maximum voiding pressure, the activity of C-kit/SCF and TGF-β/Wnt/β-catenin pathways were increased significantly in the CP group. Resveratrol treatment significantly improved these factors.

Conclusion: CP induced significantly prostate fibrosis, which exhibits a close relationship with urinary dysfunction. Resveratrol improved fibrosis, which may be associated with the suppression of C-kit/SCF and TGF-β/Wnt/β-catenin pathway.

Keywords: Chronic prostatitis; Fibrosis; Resveratrol; SCF/C-kit; Urinary dysfunction.

MeSH terms

  • Animals
  • Chronic Disease
  • Fibrosis
  • Male
  • Prostate / drug effects
  • Prostate / metabolism
  • Prostate / pathology
  • Prostatitis / drug therapy*
  • Prostatitis / metabolism
  • Prostatitis / pathology
  • Prostatitis / physiopathology
  • Proto-Oncogene Proteins c-kit / metabolism
  • Rats, Sprague-Dawley
  • Resveratrol
  • Stem Cell Factor / metabolism
  • Stilbenes / pharmacology
  • Stilbenes / therapeutic use*
  • Transforming Growth Factor beta / metabolism
  • Urinary Bladder, Overactive / drug therapy*
  • Urinary Bladder, Overactive / metabolism
  • Urinary Bladder, Overactive / pathology
  • Urinary Bladder, Overactive / physiopathology
  • Wnt Proteins / metabolism
  • beta Catenin / metabolism

Substances

  • Ctnnb1 protein, rat
  • Stem Cell Factor
  • Stilbenes
  • Transforming Growth Factor beta
  • Wnt Proteins
  • beta Catenin
  • Proto-Oncogene Proteins c-kit
  • Resveratrol