Developing a Long-lasting Tyrosinase Inhibitor from Morus alba L.

Feb 28, 2006 | Contact Author | By: Michelle Kim, Xiaofeng Meng, PhD and Abraham Kim, Tim and Cross Inc.; Mingfu Wang, PhD, Hong Kong University; and James E. Simon, PhD, Rutgers State University
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Title: Developing a Long-lasting Tyrosinase Inhibitor from Morus alba L.
skin whiteningx tyrosinasex melaninx Morus albax mulberroside Ax
  • Article

There are various causes for the darkening of skin color, UV rays considered the primary source. When skin is exposed to UV rays, melanin is synthesized in melanocytes and released to darken the skin. Melanin pigmentation in human skin is a major defense mechanism against UV light from the sun, but abnormal pigmentation such as freckles or chloasma can be a serious aesthetic problem. Tyrosinase and other proteins, such as tyrosinase-related protein 1 (Tyrp-1) and tyrosinase-related protein 2 (Tyrp-2, Dopachrome tautomerase), are responsible for the biosynthesis of melanin. Among these enzymes, tyrosinase plays the most important role in melanin synthesis. Tyrosinase is a copper-containing enzyme and is expressed exclusively in melanocytes, the melanin-producing cells in the epidermis. Tyrosinase itself can produce melanin pigments in the absence of other melanogenic enzymes. In fact, fi broblast cells transfected with tyrosinase cDNA produce melanin in their lysosome-like structures. It is not fully understood how the expression of tyrosinase is regulated. Studies are being conducted to discover melanogenic inhibitory compounds to prevent or to cure these hyperpigmentary disorders with tyrosinase as the major target. 

Excerpt Only This is a shortened version or summary of the article that appeared in the March 2006 issue of Cosmetics & Toiletries magazine. If you would like a copy of the complete article, please contact us at customerservice@cosmeticsandtoiletries.com.