Topically delivered nitric oxide acts synergistically with an orally administered PDE5 inhibitor in eliciting an erectile response in a rat model of radical prostatectomy

Int J Impot Res. 2022 Sep;34(6):573-580. doi: 10.1038/s41443-021-00451-6. Epub 2021 May 20.

Abstract

Patients undergoing radical prostatectomy (RP) have a high incidence of postoperative erectile dysfunction (ED) refractory to treatment by oral phosphodiesterase-5 inhibitors (PDE5i). In the present studies, we investigated if a topically applied, nitric oxide microparticle delivery system (NO-MP) might act synergistically with an oral PDE5i (sildenafil) to improve erectile function outcomes in a rat model of RP. Thirty-five Sprague-Dawley rats underwent bilateral transection of the cavernous nerve (CN) for 1 week. After 1 week, animals were orally administered 0, 0.05, or 0.005 mg sildenafil/kg and the erectile response following topical application to the penile shaft of 250 or 100 mg NO-MP, or blank-MP, was monitored over a 2-h timeframe by recording the intracorporal pressure normalized to systemic blood pressure (ICP/BP, N = 5 animals/treatment group). Oral treatment with sildenafil by itself resulted in no observable erectile response. However, a combination of orally administered 0.05 sildenafil/kg with topical application of 250 mg NO-MP, compared to 250 mg NO-MP by itself, resulted in significantly more spontaneous erections (4.6 compared to 2 erections per hour, t-test; p value = 0.043), with a significantly faster onset for the first erectile response (11 compared to 22 min; t-test, p value = 0.041). Our results demonstrate a synergistic effect between orally administered PDE5i and topically applied NO-MP in eliciting an erectile response. Furthermore, they suggest a potential novel therapeutic approach to treat men with ED resulting from RP, through combination therapy of a topically applied NO-MP and an orally administered PDE5i.

MeSH terms

  • Animals
  • Cyclic Nucleotide Phosphodiesterases, Type 5 / pharmacology
  • Cyclic Nucleotide Phosphodiesterases, Type 5 / therapeutic use
  • Erectile Dysfunction* / drug therapy
  • Erectile Dysfunction* / etiology
  • Humans
  • Male
  • Nitric Oxide
  • Penile Erection
  • Phosphodiesterase 5 Inhibitors* / pharmacology
  • Phosphodiesterase 5 Inhibitors* / therapeutic use
  • Prostatectomy / adverse effects
  • Rats
  • Rats, Sprague-Dawley
  • Sildenafil Citrate / pharmacology
  • Sildenafil Citrate / therapeutic use

Substances

  • Phosphodiesterase 5 Inhibitors
  • Nitric Oxide
  • Sildenafil Citrate
  • Cyclic Nucleotide Phosphodiesterases, Type 5