A novel reuptake inhibitor, IP2015, induces erection by increasing central dopamine and peripheral nitric oxide release

Br J Pharmacol. 2024 Aug;181(15):2566-2582. doi: 10.1111/bph.16362. Epub 2024 Apr 11.

Abstract

Background and purpose: An estimated 40% of patients with erectile dysfunction have a poor prognosis for improvement with currently available treatments. The present study investigated whether a newly developed monoamine transport inhibitor, IP2015, improves erectile function.

Experimental approach: We investigated the effects of IP2015 on monoamine uptake and binding, erectile function in rats and diabetic mice and the effect on corpus cavernosum contractility.

Key results: IP2015 inhibited the uptake of 5-HT, noradrenaline and dopamine by human monoamine transporters expressed in cells and in rat brain synaptosomes. Intracavernosal pressure measurement in anaesthetized rats revealed that IP2015 dose-dependently increased the number and the duration of spontaneous erections. Whereas pretreatment with the dopamine D2-like receptor antagonists, clozapine and (-)-sulpiride, or cutting the cavernosal nerve inhibited IP2015-induced erectile responses, the phosphodiesterase type 5 inhibitor sildenafil further enhanced the IP2015-mediated increase in intracavernosal pressure. IP2015 also increased the number of erections in type 2 diabetic db/db mice. Direct intracavernosal injection of IP2015 increased penile pressure, and in corpus cavernosum strips, IP2015 induced concentration-dependent relaxations. These relaxations were enhanced by sildenafil and blunted by endothelial cell removal, a nitric oxide synthase inhibitor, NG-nitro-l-arginine and a D1-like receptor antagonist, SCH23390. Quantitative polymerase chain reaction (qPCR) showed the expression of the dopamine transporter in the rat corpus cavernosum.

Conclusion and implications: Our findings suggest that IP2015 stimulates erectile function by a central mechanism involving dopamine reuptake inhibition and direct NO-mediated relaxation of the erectile tissue. This novel multi-modal mechanism of action could offer a new treatment approach to erectile dysfunction.

Keywords: IP2015; dopamine; dopamine transporter; endothelium; erection; mice; rats.

MeSH terms

  • Animals
  • Dopamine* / metabolism
  • Dose-Response Relationship, Drug
  • Erectile Dysfunction / drug therapy
  • Erectile Dysfunction / metabolism
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nitric Oxide* / metabolism
  • Penile Erection* / drug effects
  • Penis / drug effects
  • Penis / metabolism
  • Piperazines / pharmacology
  • Rats
  • Rats, Sprague-Dawley*

Substances

  • Dopamine
  • Nitric Oxide
  • vanoxerine
  • Piperazines