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DOI QR Code

Inhibitory Effects of Ethanol Extract from Angelica tenuissima Root on Oxidative Stress and Melanogenesis

  • Koo, Hyun Jung (Department of Medicinal and Industrial Crops, Korea National College of Agriculture and Fisheries) ;
  • Lee, Sung Ryul (Department of Convergence Biomedical Science, Cardiovascular and Metabolic Disease Center, College of Medicine, Inje University) ;
  • Park, Yuna (Department of Herbal Medicine Resource, Kangwon National University) ;
  • Lee, Jin Woo (Department of Herbal Medicine Resource, Kangwon National University) ;
  • So, Gyeongseop (Department of Herbal Medicine Resource, Kangwon National University) ;
  • Kim, Sung Hyeok (Department of Herbal Medicine Resource, Kangwon National University) ;
  • Ha, Chang Woo (Department of Herbal Medicine Resource, Kangwon National University) ;
  • Lee, Sang Eun (Department of Herbal Medicine Resource, Kangwon National University) ;
  • Bak, Jong Phil (Department of Herbal Medicine Resource, Kangwon National University) ;
  • Ham, Su Ryeon (Korea Research Institute Bio Science Co., Ltd.) ;
  • Lim, Hyosun (Korea Research Institute Bio Science Co., Ltd.) ;
  • Kim, Youn Kyu (Korea Research Institute Bio Science Co., Ltd.) ;
  • Sohn, Eun-Hwa (Department of Herbal Medicine Resource, Kangwon National University)
  • 투고 : 2018.06.01
  • 심사 : 2018.07.06
  • 발행 : 2018.08.31

초록

Angelica tenuissima, also known as Ligusticum tenuissimum, is classified as a food-related plant and has been used as traditional medicines treating headache and anemia in Asia. However, its anti-melanogenic effect has not been reported in detail. When the extract of Angelica tenuissima (ATE) was prepared by the extraction with 70% EtOH at $80^{\circ}C$ (final yield = 22%), the contents of decursin and Z-ligustilide in ATE were determined 0.06% and 8.43%, respectively. Total flavonoid and phenolic content in mg ATE were $5.52{\pm}0.07{\mu}g$ quercetin equivalents and $237.27{\pm}13.24{\mu}g$ gallic acid equivalents, respectively. Antioxidant capacity of ATE determined by DPPH and ABTS assay was increased with a dose dependent manner up to $1000{\mu}g/m{\ell}$. The amount of melanin synthesis followed by ${\alpha}-melanocyte$ stimulating hormone on B16F10 cells were significantly reduced in the presence of ATE (250 to $1000{\mu}g/m{\ell}$, p<0.05). ATE (125 to $1000{\mu}g/m{\ell}$, p<0.05) suppressed the tyrosinase activity but did not show any significant effect on ${\alpha}-glucosidase$ activity at the same condition. Taken together, ATE possesses tyrosinase inhibitory potential with significant antioxidant capacities. These effects of ATE might be involved in suppression of melanin synthesis, at least, in B16F10 cells. The anti-melanogenic potential of ATE will provide an insight into developing a new skin whitening product.

키워드

참고문헌

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