Browse > Article
http://dx.doi.org/10.3746/jkfn.2014.43.5.705

Hypopigmenting Effects of Extracts from Bulbs of Lilium Oriental Hybrid 'Siberia' in Murine B16/F10 Melanoma Cells  

Yoon, Hoon Seok (Cosmetic Science Center, Dept. of Chemistry, Jeju National University)
Yang, Kyung-Wol (Jeju Love Co., Ltd.)
Kim, Jung Eun (Cosmetic Science Center, Dept. of Chemistry, Jeju National University)
Kim, Jeong Mi (Jeju Love Co., Ltd.)
Lee, Nam Ho (Cosmetic Science Center, Dept. of Chemistry, Jeju National University)
Hyun, Chang-Gu (Cosmetic Science Center, Dept. of Chemistry, Jeju National University)
Publication Information
Journal of the Korean Society of Food Science and Nutrition / v.43, no.5, 2014 , pp. 705-711 More about this Journal
Abstract
In order to develop a skin-whitening agent, melanin contents and intracellular tyrosinase activity were determined by western blotting. Ethyl acetate fractions of 80% ethanol extracts from lily (Lilium Oriental Hybrid 'Siberia') bulbs (R-EA) inhibited melanin synthesis in a dose-dependent manner in ${\alpha}$-melanocyte stimulating hormone (${\alpha}$-MSH)-treated B16/F10 murine melanoma cells. Intracellular tyrosinase activity and melanin contents were suppressed by 45% and 74%, respectively, in response to treatment with $100{\mu}g/mL$ of R-EA. Examination of protein expression associated with ${\alpha}$-MSH-induced melanogenesis showed that tyrosinase related protein (TRP)-1 was inhibited more strongly than tyrosinase, and these results were correlated with stronger inhibition of melanin synthesis than intracellular tyrosinase activity. Taken together, R-EA containing p-coumaric acid and resveratrol could be used as a hypopigmentation agent through suppression of sustained extracellular signal-regulated kinase (ERK) activation via melanogenic induction.
Keywords
lily bulbs; hypopigmentation; melanin; extracellular signal-regulated kinase;
Citations & Related Records
Times Cited By KSCI : 3  (Citation Analysis)
연도 인용수 순위
1 Lee TH, Seo JO, Baek SH, Kim SY. 2014. Inhibitory effects of resveratrol on melanin synthesis in ultraviolet B-induced pigmentation in Guinea pig skin. Biomol Ther (Seoul) 22: 35-40.   과학기술학회마을   DOI   ScienceOn
2 Ndiaye M, Philippe C, Mukhtar H, Ahmad N. 2011. The grape antioxidant resveratrol for skin disorders: promise, prospects, and challenges. Arch Biochem Biophys 508: 164-170.   DOI
3 Yoon HS, Lee SR, Ko HC, Choi SY, Park JG, Kim JK, Kim SJ. 2009. Involvement of extracellular signal-regulated kinase in nobiletin-induced melanogenesis in murine B16/F10 melanoma cells. Biosci Biotechnol Biochem 71: 1781-1784.
4 Hsieh TC, Wu JM. 2010. Resveratrol: biological and pharmaceutical properties as anticancer molecule. Biofactors 36: 360-369.   DOI
5 Kim HK, Han HS, Lee GD, Kim KH. 2005. Physiological activities of fresh Pleurotus eryngii extracts. J Korean Soc Food Sci Nutr 34: 439-445.   과학기술학회마을   DOI
6 Abel EL, Angel JM, Kiguchi K, DiGiovanni J. 2009. Multistage chemical carcinogenesis in mouse skin: fundamentals and applications. Nat Protoc 4: 1350-1362.   DOI   ScienceOn
7 Driedger PE, Blumberg PM. 1980. Specific binding of phorbol ester tumor promoters. Proc Natl Acad Sci USA 77: 567-571.   DOI   ScienceOn
8 Hearing VJ, Tsukamoto K. 1991. Enzymatic control of pigmentation in mammals. FASEB J 5: 2902-2909.
9 Imokawa G, Kobayashi T, Miyagishi M, Higashi K, Yada Y. 1997. The role of endothelin-1 in epidermal hyperpigmentation and signaling mechanisms of mitogenesis and melanogenesis. Pigment Cell Res 10: 218-228.   DOI   ScienceOn
10 Thody AJ, Graham A. 1998. Does alpha-MSH have a role in regulating skin pigmentation in humans? Pigment Cell Res 11: 265-274.   DOI   ScienceOn
11 Gilchrest BA, Park HY, Eller MS, Yaar M. 1996. Mechanisms of ultraviolet light-induced pigmentation. Photochem Photobiol 63: 1-10.   DOI   ScienceOn
12 Tsukamoto K, Jackson IJ, Urabe K, Montague PM, Hearing VJ. 1992. A second tyrosinase-related protein, TRP-2, is a melanogenic enzyme termed DOPAchrome tautomerase. EMBO J 11: 519-526.
13 Briganti S, Camera E, Picardo M. 2003. Chemical and instrumental approaches to treat hyperpigmentation. Pigment Cell Res 16: 101-110.   DOI   ScienceOn
14 Yoon HS, Kim JK. 2007. The inhibitory effect of Acanthopeltis japonica on melanogenesis. J Soc Cosmet Sci Korea 33: 87-92.
15 Yoon HS, Kim JK, Kim SJ. 2007. The inhibitory effect on the melanin synthesis in B16/F10 mouse melanoma cells by Sasa quelpaertensis leaf extract. Korean J Life Sci 17: 873-875.   과학기술학회마을   DOI
16 Tsukida K, Ikeuchi K. 1965. Epoxycarotenoids. VIII. Pollen carotenoids of Lilium longiflorum and of its cultivated hybrid. Bitamin 32: 222-226.
17 Mimaki Y, Nakamura O, Sashida Y, Satomi Y, Nishino A, Nishino H. 1994. Steroidal saponins from the bulbs of Lilium longiflorum and their antitumour-promoter activity. Phytochemistry 37: 227-232.   DOI   ScienceOn
18 Shoyama Y, Hatano K, Nishioka I, Yamagishi T. 1987. Phenolic glycosides from Lilium longiflorum. Phytochemistry 26: 2965-2968.   DOI   ScienceOn
19 Francis JA, Rumbeiha W, Nair MG. 2004. Constituents in Easter lily flowers with medicinal activity. Life Sci 76: 671-683.   DOI   ScienceOn
20 Hill HZ, Li W, Xin P, Michell DL. 1997. Melanin: a two edged sword? Pigment Cell Res 10: 158-161.   DOI   ScienceOn
21 Esposito D, Munafo JP Jr, Lucibello T, Baldeon M, Kormarnytsky S, Gianfagna TJ. 2013. Steroidal glycosides from the bulbs of Easter lily (Lilium longiflorum Thunb.) promote dermal fibroblast migration in vitro. J Ethnopharmacol 148: 433-440.   DOI   ScienceOn
22 Munafo JP Jr, Ramanathan A, Jimenez LS, Gianfagna TJ. 2010. Isolation and structural determination of steroidal glycosides from the bulbs of easter lily (Lilium longiflorum Thunb.). J Agric Food Chem 58: 8806-8813.   DOI   ScienceOn
23 An SM, Lee SI, Choi SW, Moon SW, Boo YC. 2008. p-Coumaric acid, a constituent of Sasa quelpaertensis Nakai, inhibits cellular melanogenesis stimulated by ${\alpha}$-melanocyte stimulating hormone. Br J Dermatol 159: 292-299.   DOI   ScienceOn