Hormonal & Sexual Health

PT-141

Bremelanotide (PT-141)

A melanocortin receptor agonist developed from Melanotan II. FDA-approved (as Vyleesi) for hypoactive sexual desire disorder in premenopausal women. Used off-label for sexual dysfunction in both sexes.

Sexual HealthLibidoMelanocortinArousal

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Category
Hormonal & Sexual Health
Research Claims
3 reviewed
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Mechanism of Action

PT-141 activates melanocortin receptors (MC3R and MC4R) in the central nervous system, directly stimulating sexual arousal pathways in the brain. Unlike PDE5 inhibitors, it works centrally rather than through vascular mechanisms.

Health Claims & Evidence

Increases sexual desire and arousal

StrongFDA-approved for HSDD; multiple clinical trials confirm efficacy

Effective for both male and female sexual dysfunction

Moderateclinical trials in both sexes show improvement

Works independently of vascular mechanisms

Strongcentral CNS mechanism distinct from PDE5 inhibitors

Short-Term Effects

Increased sexual desire and arousal within 45–60 minutes. Effects last 6–12 hours.

Long-Term Effects

No tolerance development reported. Suitable for as-needed use.

Side Effects

Nausea (most common), flushing, headache, transient blood pressure increase, hyperpigmentation with repeated use.

Contraindications

Avoid with cardiovascular disease or uncontrolled hypertension.

This profile is provided for educational research only. It is not a treatment recommendation or dosing guide. Human evidence, safety information and regulatory status vary by substance. Verify primary sources and consult a qualified healthcare professional for medical decisions.

Research Papers

Bremelanotide for hypoactive sexual desire disorder

Clayton et al. · Obstetrics & Gynecology · 2016

Educational research only. This profile is not a treatment recommendation or dosing guide. Human evidence, safety information and regulatory status vary by substance. Consult a qualified healthcare professional for medical decisions.

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