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PT-141

Bremelanotide, Vyleesi

Quick Stats
Studies 74
Trials 10
Score 4
2006 pubmed 109 citations

An effect on the subjective sexual response in premenopausal women with sexual arousal disorder by bremelanotide (PT-141), a melanocortin receptor agonist.

Diamond. Lisa E LE; Earle. Dennis C DC; Heiman. Julia R JR; Rosen. Raymond C RC; Perelman. Michael A MA; Harning. Ronald R

Key Findings

  • More women reported moderate or high sexual desire after bremelanotide compared to placebo (p = 0.0114).
  • Women who tried sex within 24 hours were more satisfied with their arousal after bremelanotide (p = 0.0256).
  • Vaginal vasocongestion (blood flow) measured during erotic videos did not differ between bremelanotide and placebo.

Practical Outcomes

  • For self‑experimenters, a 20 mg intranasal dose of PT‑141 appears to be a quick way to raise sexual desire and subjective arousal in women without major side effects. The effect is mainly felt subjectively, so users should track personal satisfaction rather than rely on physiological metrics. More research is needed, but this protocol can be tried in a controlled, at‑home setting with proper medical supervision.

Summary

A single 20 mg intranasal dose of bremelanotide (PT‑141) gave pre‑menopausal women with sexual arousal disorder a noticeable boost in sexual desire and made them feel more satisfied with their arousal, even though the objective measure of vaginal blood flow didn't change.

Abstract

Melanocortins affect multiple physiological responses, including sexual behaviors. Bremelanotide is a synthetic peptide melanocortin analog of alpha-melanocyte-stimulating hormone that is an agonist at melanocortin receptors MC3R and MC4R. To evaluate a single intranasal dose of bremelanotide for potential effects on physiological and subjective measurements of sexual arousal and desire in premenopausal women with sexual arousal disorder. Change in vaginal pulse amplitude during neutral and erotic videos after treatment with bremelanotide or placebo and subjects' perceptions of physiological and sexual response within 24 hours of treatment with bremelanotide or placebo. Eighteen premenopausal women with a primary diagnosis of female sexual arousal disorder were randomly assigned to receive a single intranasal dose of 20 mg bremelanotide or matching placebo in a double-blind manner during the first in-clinic treatment session, and the alternate medication during the second in-clinic treatment session. During each session, subjects viewed a 20-minute neutral video followed by a 20-minute sexually explicit video. Vaginal photoplethysmography was used to monitor vaginal vasocongestion and questionnaires were used to evaluate perceptions of sexual response within the following 24-hour period. More women reported moderate or high sexual desire following bremelanotide treatment vs. placebo (P = 0.0114), and a trend toward more positive responses regarding feelings of genital arousal occurred after bremelanotide compared with placebo (P = 0.0833). Among women who attempted sexual intercourse within 24 hours after treatment, significantly more were satisfied with their level of sexual arousal following bremelanotide, compared with placebo (P = 0.0256). Vaginal vasocongestion did not change significantly while viewing erotic videos following bremelanotide administration compared with placebo. This preliminary evaluation suggests the potential for bremelanotide to positively affect desire and arousal in women with female sexual arousal disorder and indicates that bremelanotide is a promising candidate for further evaluation in an at-home study.

Study Information

Provider

pubmed

Year

2006

Date

2006-07-01T00:00:00.000Z

DOI

10.1111/j.1743-6109.2006.00268.x

Citations

109

References

45