AI Article Synopsis

  • Previous studies show that the aerial part of a certain plant has anti-melanogenic properties, but its color limits commercial use; however, an improved extract (GALM-DC) was made using activated carbon.
  • Neobavaisoflavone (NBI), identified from GALM-DC, was found to effectively reduce melanin synthesis and tyrosinase activity in B16F10 cells by decreasing the expression of key proteins involved in melanogenesis.
  • NBI operates through the MEK/ERK and Akt/GSK-3β signaling pathways and shows promise as a skin-whitening agent for treating hyperpigmentation in human skin models.

Article Abstract

Previous studies have confirmed the anti-melanogenic effect of the aerial part of , however, due to its inherent color, has limited commercial use. In this study, an extract (GALM-DC) of the aerial part of having improved color by the use of activated carbon was obtained. Furthermore, the active compound neobavaisoflavone (NBI) was identified from GALM-DC. The effect of NBI on melanogenesis, tyrosinase activity, α-glucosidase activity, and mechanism of action in melanocytes was investigated. Tyrosinase activity, melanin contents and the expression of melanin-related genes and proteins were determined in B16F10 cells. NBI reduced melanin synthesis and tyrosinase activity. Furthermore, NBI treatment reduced the mRNA and protein expression levels of MITF, TRP-1, and tyrosinase. NBI also works by phosphorylating and activating proteins that inhibit melanogenesis, such as GSK3β and ERK. Specific inhibitors of Akt/GSK-3β (LY294002) and MEK/ERK (PD98059) signaling prevented the inhibition of melanogenesis by NBI. NBI inhibited melanin production through the regulation of MEK/ERK and Akt/GSK-3β signaling pathways in α-MSH-stimulated B16F10 cells. NBI suppresses tyrosinase activity and melanogenesis through inhibition of α-glucosidase activity. Besides, NBI significantly reduced melanogenesis in a reconstructed human 3D skin model. In conclusion, these results suggest that NBI has potential as a skin-whitening agent for hyperpigmentation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7321173PMC
http://dx.doi.org/10.3390/molecules25112683DOI Listing

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