Endothelial effects of drugs designed to treat erectile dysfunction

Antonio Aversa, Massimiliano Caprio, Giuseppe M C Rosario, Giovanni Spera

Research output: Contribution to journalArticlepeer-review


Erectile dysfunction (ED) and endothelial dysfunction are common in individuals with multiple cardiovascular risk factors (CRFs) and are longitudinal predictors of cardiovascular events. ED is associated with systemic endothelial cell activation/dysfunction independent from CRFs or from diffuse, unrecognized vascular damage. The pathogenesis of endothelial dysfunction and ED is intimately linked through decreased expression and activation of endothelial nitric oxide (NO) synthase and the subsequent physiologic actions of NO. Furthermore, reduced biologic activity of endothelium-derived NO links atherosclerosis to ED and underscores the role of altered endothelium in the pathogenesis of both conditions. Evidence-based data suggest that daily use of phosphodiesterase type-5, inhibitors (PDE5-i) improves endothelial and erectile functions and that this benefit is lost upon drug withdrawal. Daily PDE5-i may also improve lower tract urinary symptoms related to benign prostatic hyperplasia through a reduction of adrenergic overtone. The relevance for these drugs in the prevention of complications in internal medicine diseases, i.e. cardiovascular disease, clotting disorders and autoimmune disease is uncertain. Finally, endothelial dysfunction is present in testosterone deficiency syndromes and replacement therapy is able to revert ED and to improve endothelial function. Aim ofthe present review is to discuss the systemic effects ofdrugs designed to treat ED, such as testosterone and PDE5i, with regard to safety, unwanted effects and efficacy in improving endothelial function; finally, a goal-oriented approach to rehabilitation using daily vs. on-demand PDE5-i in difficult patients is discussed.

Original languageEnglish
Pages (from-to)3768-3778
Number of pages11
JournalCurrent Pharmaceutical Design
Issue number35
Publication statusPublished - 2008


  • Benign prostatic hyperplasia
  • Endothelial dysfunction
  • Internal medicine
  • LUTS
  • Nitric oxide
  • Phosphodiesterase type-5 inhibitors
  • Rehabilitation
  • Testosterone

ASJC Scopus subject areas

  • Drug Discovery
  • Pharmacology


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