[Nle4-D-Phe7]-alpha-melanocyte-stimulating hormone significantly increased pigmentation and decreased UV damage in fair-skinned Caucasian volunteers.
Barnetson. Ross StC RS; Ooi. Terry K T TK; Zhuang. Liqing L; Halliday. Gary M GM; Reid. Catherine M CM; Walker. Patrick C PC; Humphrey. Stuart M SM; Kleinig. Michael J MJ
Key Findings
- MelanotanâI increased skin melanin significantly, especially in lowâbaseline melanin individuals (â41% rise).
- In lowâMED (burnâprone) skin, sunburn cell formation after high UV exposure dropped >50% after treatment.
- Thymineâdimer DNA damage in the epidermis fell by 59% after melanotanâI administration.
Practical Outcomes
- For biohackers, melanotanâI can be used as a subâcutaneous protocol (0.16âŻmg/kg, three 10âday cycles) to enhance tanning and potentially lower UVâinduced skin damage. Expect the biggest pigment boost if you start with very light skin. Monitor for side effects and remember this is still earlyâstage research, not an approved sunscreen substitute.
Summary
A study gave a synthetic hormone called melanotanâI (0.16âŻmg per kg body weight, injected under the skin in three 10âday rounds over three months) to fairâskinned volunteers. It made their skin much darker, especially in people who started with very little melanin, and cut sunburn cell damage by more than half and DNA damage by about 60%. This suggests melanotanâI can boost natural tanning and give real UV protection, but itâs still an experimental approach.
Abstract
Epidermal melanin reduces some effects of UV radiation, the major cause of skin cancer. To examine whether induced melanin can provide protection from sunburn injury, 65 subjects completed a trial with the potent synthetic melanotropin, [Nle4-D-Phe7]-alpha-melanocyte-stimulating hormone ([Nle4-D-Phe7]-alpha-MSH) delivered by subcutaneous injection into the abdomen at 0.16 mg/kg for three 10-day cycles over 3 months. Melanin density, measured by reflectance spectroscopy, increased significantly in all [Nle4-D-Phe7]-alpha-MSH-treated subjects. The highest increases were in volunteers with lowest baseline skin melanin levels. In subjects with low minimal erythemal dose (MED) skin type, melanin increased by an average of 41% (from 2.55 to 3.59, P < 0.0001 vs placebo) over eight separate skin sites compared with only 12% (from 4.18 to 4.70, P < 0.0001 vs placebo) in subjects with a high-MED skin type. Epidermal sunburn cells resulting from exposure to 3 MED of UV radiation were reduced by more than 50% after [Nle4-D-Phe7]-alpha-MSH treatment in the volunteers with low baseline MED. Thymine dimer formation was also shown to be reduced by 59% (P = 0.002) in the epidermal basal layer. This study has shown for the first time the potential ability of a synthetic hormone that augments melanin production to provide photoprotection to people who normally burn in direct sunlight.
Study Information
pubmed
2006
2006-06-08T00:00:00.000Z
10.1038/sj.jid.5700317