The Impact of Vitamin D on Skin Aging

The active metabolites of vitamin D-3 (D-3) and lumisterol (L-3) exert a variety of antiaging and photoprotective effects on the skin. These are achieved through immunomodulation and include anti-inflammatory actions, regulation of keratinocytes proliferation, and differentiation programs to build the epidermal barrier necessary for maintaining skin homeostasis. In addition, they induce antioxidative responses, inhibit DNA damage and induce DNA repair mechanisms to attenuate premature skin aging and cancerogenesis. The mechanism of action would involve interaction with multiple nuclear receptors including VDR, AhR, LXR, reverse agonism on ROR alpha and -gamma, and nongenomic actions through 1,25D(3)-MARRS receptor and interaction with the nongenomic binding site of the VDR. Therefore, active forms of vitamin D-3 including its canonical (1,25(OH)(2)D-3) and noncanonical (CYP11A1-intitated) D-3 derivatives as well as L-3 derivatives are promising agents for the prevention, attenuation, or treatment of premature skin aging. They could be administrated orally and/or topically. Other forms of parenteral application of vitamin D-3 precursor should be considered to avoid its predominant metabolism to 25(OH)D-3 that is not recognized by CYP11A1 enzyme. The efficacy of topically applied vitamin D-3 and L-3 derivatives needs further clinical evaluation in future trials.

Automated summary

The active metabolites of vitamin D-3 and lumisterol have antiaging and photoprotective effects on the skin through immunomodulation, antioxidative responses, and DNA repair mechanisms. They interact with multiple nuclear receptors and have potential for preventing, attenuating, or treating premature skin aging. Further clinical evaluation of topically applied derivatives is needed for future trials.