
doi: 10.1271/bbb.110894
pmid: 22484949
Xanthium strumarium L. (Asteraceae) is traditionally used in Korea to treat skin diseases. In this study, we investigated the effects of a X. strumarium stem extract on melanin synthesis. It inhibited melanin synthesis in a concentration-dependent manner, but it did not directly inhibit tyrosinase, the rate-limiting melanogenic enzyme, and instead downregulated microphthalmia-associated transcription factor (MITF) and tyrosinase expression. MITF, the master regulator of pigmentation, is a target of the Wnt signaling pathway, which includes glycogen synthase kinase 3β (GSK3β) and β-catenin. Hence, the influence of X. strumarium stem extract on GSK3β and β-catenin was further investigated. X. strumarium induced GSK3β phosphorylation (inactivation), but the level of β-catenin did not change. Moreover, a specific GSK3β inhibitor restored X. strumarium-induced melanin reduction. Hence, we suggest that X. strumarium inhibits melanin synthesis through downregulation of tyrosinase via GSK3β phosphorylation.
Melanins, Microphthalmia-Associated Transcription Factor, Glycogen Synthase Kinase 3 beta, Dose-Response Relationship, Drug, Plant Stems, Monophenol Monooxygenase, Pigmentation, Plant Extracts, Down-Regulation, Xanthium, Glycogen Synthase Kinase 3, Mice, Animals, Melanocytes, Phosphorylation, Wnt Signaling Pathway, beta Catenin, Cell Line, Transformed
Melanins, Microphthalmia-Associated Transcription Factor, Glycogen Synthase Kinase 3 beta, Dose-Response Relationship, Drug, Plant Stems, Monophenol Monooxygenase, Pigmentation, Plant Extracts, Down-Regulation, Xanthium, Glycogen Synthase Kinase 3, Mice, Animals, Melanocytes, Phosphorylation, Wnt Signaling Pathway, beta Catenin, Cell Line, Transformed
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