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A Zn(II)–glycine complex suppresses UVB‐induced melanin production by stimulating metallothionein expression
Author(s) -
Ochiai Y.,
Kaburagi S.,
Okano Y.,
Masaki H.,
Ichihashi M.,
Funasaka Y.,
Sakurai H.
Publication year - 2008
Publication title -
international journal of cosmetic science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.532
H-Index - 62
eISSN - 1468-2494
pISSN - 0142-5463
DOI - 10.1111/j.1468-2494.2007.00423.x
Subject(s) - melanocyte , melanin , oxidative stress , reactive oxygen species , chemistry , epidermis (zoology) , keratinocyte , metallothionein , human skin , microbiology and biotechnology , photoprotection , microphthalmia associated transcription factor , biochemistry , biology , tyrosinase , cancer research , in vitro , enzyme , anatomy , melanoma , genetics , gene , photosynthesis
Synopsis Oxidative stress caused by ultraviolet (UV) radiation generates reactive oxygen species (ROS) in the skin, induces the secretion of melanocyte growth and activating factors from keratinocytes, which results in the formation of cutaneous hyper‐pigmentation. Thus, increasing the anti‐oxidative ability of skin cells is expected to be a good strategy for skin‐lightening cosmetics. Metallothionein (MT) is one of the stress‐induced proteins and is known to exhibit a strong anti‐oxidative property. We previously reported that a zinc(II) complex with glycine (Zn(II)(Gly) 2 ) effectively induces MT expression in cultured human keratinocytes. To determine its potential as a new skin lightening active, we examined whether Zn(II)(Gly) 2 regulates the release of melanocyte‐activating factors from UVB‐irradiated keratinocytes and affects melanin production in a reconstructed human epidermal equivalent. Conditioned medium from UVB‐irradiated keratinocytes accelerated melanocyte proliferation to 110%, and that increase could be prevented by pre‐treatment with Zn(II)(Gly) 2 . In addition, Zn(II)(Gly) 2 significantly reduced both the production of prostaglandin E 2 and proopiomelanocortin expression in UVB‐irradiated keratinocytes. Zn(II)(Gly) 2 also decreased melanin production in a reconstructed human epidermal equivalent. These results indicate that MT‐induction in the epidermis effectively up‐regulates tolerance against oxidative stress and inhibits the secretion of melanocyte growth and activating factors from keratinocytes. Thus, Zn(II)(Gly) 2 is a good candidate as a new skin‐lightening active.