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  2. Mechanistic studies of anti-hyperpigmentary compounds: elucidating their inhibitory and regulatory actions

Mechanistic studies of anti-hyperpigmentary compounds: elucidating their inhibitory and regulatory actions

  • Int J Mol Sci. 2014 Aug 21;15(8):14649-68. doi: 10.3390/ijms150814649.
Rosanna Y Y Lam 1 Zhi-Xiu Lin 2 Elena V Sviderskaya 3 Christopher H K Cheng 4
Affiliations

Affiliations

  • 1 School of Chinese Medicine, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China. [email protected].
  • 2 School of Chinese Medicine, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China. [email protected].
  • 3 Faculty of Medicine and Biomedical Sciences, St. George's, University of London, Cranmer Terrace, London SW17 0RE, UK. [email protected].
  • 4 School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China. [email protected].
Abstract

Searching for depigmenting agents from natural sources has become a new direction in the cosmetic industry as Natural Products are generally perceived as relatively safer. In our previous study, selected Chinese medicines traditionally used to treat hyperpigmentation were tested for anti-hyperpigmentary effects using a melan-a Cell Culture model. Among the tested chemical compounds, 4-ethylresorcinol, 4-ethylphenol and 1-tetradecanol were found to possess hypopigmentary effects. Western blot analysis, Reverse Transcriptase polymerase chain reaction (RT-PCR), cyclic adenosine monophosphate (cAMP) assay, protein kinase A (PKA) activity assay, Tyrosinase inhibition assay and lipid peroxidation inhibition assay were performed to reveal the underlying cellular and molecular mechanisms of the hypopigmentary effects. 4-Ethylresorcinol and 4-ethylphenol attenuated mRNA and protein expression of tyrosinase-related protein (TRP)-2, and possessed antioxidative effect by inhibiting lipid peroxidation. 1-Tetradecanol was able to attenuate protein expression of Tyrosinase. The hypopigmentary actions of 4-ethylresorcinol, 4-ethylphenol and 1-tetradecanol were associated with regulating downstream proteins along the PKA pathway. 4-Ethylresorcinol was more effective in inhibiting melanin synthesis when compared to 4-ethylphenol and 1-tetradecanol.

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