Active constituents from Sophora japonica exhibiting cellular tyrosinase inhibition in human epidermal melanocytes

Yuan Hsin Lo, Rong Dih Lin, Yi Pei Lin, Yan Ling Liu, Mei Hsien Lee

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

Aim of the Study: There is greater consumer awareness of plant-based skin-care products. Sophora japonica L. (Fabaceae) has been used traditionally as a hemostatic agent and also has skin-care and whitening benefits. The effect of the isolated active compounds of Sophora japonica L. (Fabaceae) that inhibits tyrosinase activity in human epidermal melanocytes (HEMn) was examined. Materials and methods: We used the mushroom tyrosinase inhibitory assay to isolate active constituents from the extracts. The structures of these constituents were characterized by physical and spectroscopic analyses. Cellular tyrosinase kinetics were analyzed and showed by Lineweaver-Burk plot. Results: A new compound, N-feruloyl-N′-cis-feruloyl-putrescine (8), together with four flavonoids and three putrescine derivatives were obtained after assay-guided isolation of S. japonica. In HEMn, compound 8 was minimally cytotoxic (cell viability >90% at 100 μM) and the IC50 value for suppression of cellular tyrosinase activity was estimated as 85.0 μM. Zymography analysis demonstrated the compound's concentration-dependent effects and the kinetic analysis indicated the compound's mixed-inhibitory action. Conclusions: We concluded that the new compound 8 is the most potent component of S. japonica yet discovered. Its pigment inhibition activity may be exploitable cosmetically.

Original languageEnglish
Pages (from-to)625-629
Number of pages5
JournalJournal of Ethnopharmacology
Volume124
Issue number3
DOIs
Publication statusPublished - Jul 30 2009

Fingerprint

Sophora
Monophenol Monooxygenase
Melanocytes
Skin Care
Putrescine
Fabaceae
Agaricales
Hemostatics
Flavonoids
Human Activities
Inhibitory Concentration 50
Cell Survival

Keywords

  • Fabaceae
  • Human epidermal melanocytes
  • N-Feruloyl-N′-cis-feruloyl-putrescine
  • Sophora japonica
  • Tyrosinase

ASJC Scopus subject areas

  • Pharmacology
  • Drug Discovery

Cite this

Active constituents from Sophora japonica exhibiting cellular tyrosinase inhibition in human epidermal melanocytes. / Lo, Yuan Hsin; Lin, Rong Dih; Lin, Yi Pei; Liu, Yan Ling; Lee, Mei Hsien.

In: Journal of Ethnopharmacology, Vol. 124, No. 3, 30.07.2009, p. 625-629.

Research output: Contribution to journalArticle

Lo, Yuan Hsin ; Lin, Rong Dih ; Lin, Yi Pei ; Liu, Yan Ling ; Lee, Mei Hsien. / Active constituents from Sophora japonica exhibiting cellular tyrosinase inhibition in human epidermal melanocytes. In: Journal of Ethnopharmacology. 2009 ; Vol. 124, No. 3. pp. 625-629.
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abstract = "Aim of the Study: There is greater consumer awareness of plant-based skin-care products. Sophora japonica L. (Fabaceae) has been used traditionally as a hemostatic agent and also has skin-care and whitening benefits. The effect of the isolated active compounds of Sophora japonica L. (Fabaceae) that inhibits tyrosinase activity in human epidermal melanocytes (HEMn) was examined. Materials and methods: We used the mushroom tyrosinase inhibitory assay to isolate active constituents from the extracts. The structures of these constituents were characterized by physical and spectroscopic analyses. Cellular tyrosinase kinetics were analyzed and showed by Lineweaver-Burk plot. Results: A new compound, N-feruloyl-N′-cis-feruloyl-putrescine (8), together with four flavonoids and three putrescine derivatives were obtained after assay-guided isolation of S. japonica. In HEMn, compound 8 was minimally cytotoxic (cell viability >90{\%} at 100 μM) and the IC50 value for suppression of cellular tyrosinase activity was estimated as 85.0 μM. Zymography analysis demonstrated the compound's concentration-dependent effects and the kinetic analysis indicated the compound's mixed-inhibitory action. Conclusions: We concluded that the new compound 8 is the most potent component of S. japonica yet discovered. Its pigment inhibition activity may be exploitable cosmetically.",
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