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Melanotan I (MT-I), also known as afamelanotide, is a synthetic analog of alpha-melanocyte-stimulating hormone (α-MSH), developed to stimulate melanin production and enhance pigmentation. This compound is supplied as a lyophilized powder strictly for research use only.
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Melanotan I is a linear peptide designed to bind to melanocortin receptors, especially MC1R, mimicking the biological activity of α-MSH. Its primary effect is to increase melanin synthesis in the skin, offering a potential non-UV means of pigmentation. MT-I has been clinically evaluated for its protective benefits in patients with EPP, a condition marked by painful phototoxic reactions to sunlight exposure [1]. It has shown promise as a safe and effective research tool in pigmentation and light sensitivity studies.
Melanotan I has been shown to significantly increase pain-free sun exposure time in individuals with erythropoietic protoporphyria. In a randomized clinical trial, patients receiving subcutaneous MT-I experienced enhanced pigmentation and photoprotection, resulting in a marked improvement in quality of life [1].
Studies have demonstrated that when Melanotan I is used in conjunction with low-dose UV-B exposure, it accelerates and intensifies pigmentation compared to UV-B alone. This indicates that Melanotan I may serve as a UV-sparing agent in therapeutic settings or research involving controlled pigmentation [2].
Beyond EPP, Melanotan I is being investigated for use in other UV-sensitive conditions such as solar urticaria and polymorphic light eruption. Its ability to safely stimulate melanin production suggests it may have broader implications for protecting the skin against photodamage [1].
Clinical trials have reported that Melanotan I is generally well tolerated. Most adverse events were mild, such as transient nausea or facial flushing. No significant toxicity has been reported at therapeutic research doses, supporting its continued evaluation in pigmentation studies [2].
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