Centrally acting mechanisms for the treatment of male sexual dysfunction.
Miner. Martin M MM; Seftel. Allen D AD
Key Findings
- PDE5 inhibitors often fail or lose effectiveness over time
- Central‑acting drugs are being explored as alternatives for erectile dysfunction
- Apomorphine is an example of a centrally acting agent used in Europe
Practical Outcomes
- For biohackers, the takeaway is that while brain‑targeting drugs could become a new option for sexual health, there’s currently no clear protocol or dosage guidance for pt‑141 from this article, so more research is needed before trying it.
Summary
The paper explains that many men with erectile problems don’t get enough help from the usual pills (PDE5 inhibitors) and that doctors are looking at drugs that work in the brain to improve erections, like apomorphine, but it doesn’t give specific tips for using the peptide pt‑141.
Abstract
The development of pharmacologic therapy for erectile dysfunction (ED) has been possible because of incremental growth in our understanding of the physiology of normal erections and the complex pathophysiology of ED. Although the oral phosphodiesterase type 5 (PDE5) inhibitors have provided safe, effective treatment of ED for some men, a large proportion of men who have ED do not respond to PDE5 inhibitors or become less responsive or less satisfied as the duration of therapy increases. Also, men who are receiving organic nitrates and nitrates, such as amyl nitrate, cannot take PDE5 inhibitors because of nitrate interactions. The current options for treatment beyond PDE5 inhibitors are invasive, unappealing to some patients, and sometimes ineffective. The search for other options by which ED can be treated has branched out and now encompasses centrally acting mechanisms that control erectile function. Drugs available in Europe include apomorphine. This article focuses on the mechanism of centrally acting agents and reviews clinical data on potential new centrally acting drugs for men who have ED.
Study Information
pubmed
2007
10.1016/j.ucl.2007.08.008