The Journal of pharmacy and pharmacology · 2010
Inhibitory effects of 5-chloroacetyl-2-piperidino-1,3-selenazole, a novel selenium-containing compound, on skin melanin biosynthesis.
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Lee Eunjoo H, Lim Yu-Ji, Ha Sang Keun, Kang Tong Ho, Koketsu Mamoru, Kang Chulhun, Kim Sun Yeou, Park Ji-Ho
Аннотация
OBJECTIVES: Increased production and accumulation of melanin leads to many hyperpigmentation disorders such as melasma, freckles and geriatric pigment spots. Thus, there is a need for the development of depigmenting agents. Based on our previous reports, selenium derivatives as anti-melanogenic lead compounds could be very important. The aim of this study was to investigate the depigmenting effect of novel selenium-containing compounds.
METHODS: The inhibitory effects of 5-chloroacetyl-2-piperidino-1,3-selenazole (CS1), a novel selenium-containing compound, on melanogenesis were investigated in B16F10 melanoma cells and cultured brownish guinea pig skin tissue with alpha-melanocyte-stimulating hormone stimulation.
KEY FINDINGS: We found that CS1 inhibited melanin production in B16F10 cells by suppressing tyrosinase activity and its protein expression. In addition, Western blotting analysis revealed that CS1 suppressed the expression of tyrosinase-related protein (TRP)-1 and TRP-2. Therefore, the depigmenting effect of CS1 might have been due to inhibition of tyrosinase activity and expression of melanogenic enzymes. Furthermore, CS1 had inhibitory effects on melanin biosynthesis of primary cultured skin of brownish guinea pig.
CONCLUSIONS: The results suggested that CS1 could be a useful candidate for the treatment of skin hyperpigmentation.
METHODS: The inhibitory effects of 5-chloroacetyl-2-piperidino-1,3-selenazole (CS1), a novel selenium-containing compound, on melanogenesis were investigated in B16F10 melanoma cells and cultured brownish guinea pig skin tissue with alpha-melanocyte-stimulating hormone stimulation.
KEY FINDINGS: We found that CS1 inhibited melanin production in B16F10 cells by suppressing tyrosinase activity and its protein expression. In addition, Western blotting analysis revealed that CS1 suppressed the expression of tyrosinase-related protein (TRP)-1 and TRP-2. Therefore, the depigmenting effect of CS1 might have been due to inhibition of tyrosinase activity and expression of melanogenic enzymes. Furthermore, CS1 had inhibitory effects on melanin biosynthesis of primary cultured skin of brownish guinea pig.
CONCLUSIONS: The results suggested that CS1 could be a useful candidate for the treatment of skin hyperpigmentation.
Предметные рубрики MeSH
AnimalsCell SurvivalDown-RegulationDrug Evaluation, PreclinicalEnzyme InhibitorsFungal ProteinsGuinea PigsHyperpigmentationIntramolecular OxidoreductasesMelaninsMelanomaMembrane GlycoproteinsMiceMonophenol MonooxygenaseOrgan Culture TechniquesOrganoselenium CompoundsOsmolar ConcentrationOxidoreductasesSelenium CompoundsSkinTumor Cells, Culturedalpha-MSH