Expression and functional activity of phosphodiesterase type 5 in human and rabbit vas deferens

R. Mancina, S. Filippi, M. Marini, A. Morelli, L. Vignozzi, A. Salonia, F. Montorsi, N. Mondaini, G. B. Vannelli, S. Donati, F. Lotti, G. Forti, M. Maggi

Research output: Contribution to journalArticlepeer-review

Abstract

The molecular mechanisms underlying the regulation of vas deferens (VD) motility and semen emission are still poorly understood. We now report evidence on VD expression of phosphodiesterase type 5 (PDE5), which regulates nitric oxide (NO)-induced relaxation and cGMP breakdown in smooth muscle cells. In human VD, the PDE5 abundance was relatively high (>3 × 106 molecules/μg total RNA), although 10-fold lower than in corpora cavernosa (CC). Also cGMP metabolising activity was higher in CC than in VD. However, both tissues share the same sensitivity to a broad panel of cGMP-related PDE inhibitors: sildenafil, tadalafil, dipyridamole, zaprinast, vinpocetine, EHNA and cilostamide. Based on the rank order of potency of these PDE inhibitors, we found that the cGMP metabolizing activity in human VD mostly corresponds to PDE5. PDE5 was immunolocalized in all the muscular layers of human and rabbit VD and was found to be negatively involved in regulating NO-induced relaxation. In addition, by using a rabbit model of hypogonadotropic hypogonadism, we found that PDE5 gene expression and activity are androgen-dependent in VD, as previously demonstrated in CC. In fact, the sensitivity to a NO-donor (NCX4040), its enhancement by PDE5 inhibitors and the PDE5-related cGMP breakdown were all affected by androgen manipulation. Our results provide a hypothesis explaining the beneficial effects of PDE inhibitors in patients with rapid ejaculation.

Original languageEnglish
Pages (from-to)107-115
Number of pages9
JournalMolecular Human Reproduction
Volume11
Issue number2
DOIs
Publication statusPublished - Feb 2005

Keywords

  • PDE5
  • Rapid ejaculation
  • Sildenafil
  • Tadalafil
  • Vas deferens

ASJC Scopus subject areas

  • Obstetrics and Gynaecology
  • Genetics
  • Developmental Biology
  • Embryology
  • Cell Biology

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