Effect of Aqueous Extract from Asiasari Radix on ${\alpha}$-melanocyte Stimulating Hormone Induced Melanogenesis in B16F10 Melanoma Cells

세신의 열수추출물이 ${\alpha}$-melanocyte Stimulating Hormone에 의해 유도된 B16F10 세포의 멜라닌 생성에 미치는 영향

  • Lee, Jun-Hyuk (Chemistry and Biotechnology Examinations Bureau, Korean Intellectual Property Office) ;
  • Shin, Dong-Yeok (Departments of Biochemistry, College of Oriental Medicine, Dong-Eui University) ;
  • Choi, Yung-Hyun (Departments of Biochemistry, College of Oriental Medicine, Dong-Eui University) ;
  • Chung, Kyung-Tae (Departments of Biomedical Laboratory Science, College of Natural Science, Dong-Eui University) ;
  • Kang, Byoung-Won (Departments of Chemistry, College of Natural Science, Dong-Eui University) ;
  • Jeong, Seong-Yun (Korea BIO-IT Foundry Center) ;
  • Choi, Byung-Tae (School of Oriental Medicine, Pusan National University)
  • 이준혁 (특허청 화학생명공학심사국) ;
  • 신동역 (동의대학교 한의과대학 생화학교실) ;
  • 최영현 (동의대학교 한의과대학 생화학교실) ;
  • 정경태 (동의대학교 자연과학대학 임상병리학과) ;
  • 강병원 (동의대학교 자연과학대학 화학과) ;
  • 정성윤 (부산대학교 BIT융합기술산업화지원기반구축사업단) ;
  • 최병태 (한의학전문대학원)
  • Published : 2008.06.25

Abstract

The aqueous extract from Asiasari radix (AEAR) was used to investigate the effect of ${\alpha}$-melanocyte stimulating hormone induced melanogenesis in B16F10 mouse melnoma cells. The treatment with AEAR at the 1.0 and 2.0 mg/ml level significantly inhibited the biosynthesis of melanin without changes of cell growth and morphology compared with untreated control. The AEAR-treated cells at the 2.0 mg/ml level were more efficient than commercial arbutin at 0.1 mg/ml. The tyrosinase activity also significantly decreased in AEAR-treated cells at the 1.0 and 2.0 mg/ml level. The Western analyses confirmed the slightly decreased expression of tyrosinase by AEAR treatment. These results indicate that AEAR may contribute to the inhibition of melanin biosynthesis through regulating tyrosinase activity and expression and serve as a new candidate in the design of new skin-whitening or therapeutic agents.

Keywords

References

  1. Kim, D.S., Park, S.H., Kwon, S.B., Youn, S.W., Park, K.C. Effects of lysophosphatidic acid on melanogenesis. Chem. Phy. Lipid 127: 199-206. 2004 https://doi.org/10.1016/j.chemphyslip.2003.11.002
  2. Ito, S. The IFPCS presidential lecture: a chemist's view of melanogenesis. Pigment Cell Res 16: 230-236, 2003 https://doi.org/10.1034/j.1600-0749.2003.00037.x
  3. Baurin, N., Arnoult, E., Scior, T., Do, Q.T., Bernard, P. Preliminary screening of some tropical plants for anti-tyrosinase activity. J. Ethnopham 82: 155-158, 2002 https://doi.org/10.1016/S0378-8741(02)00174-5
  4. Hearing, V.J., Tsukamoto, K. Enzymatic control of pigmentation in mammals. FASEB J 5: 2902-2909, 1991 https://doi.org/10.1096/fasebj.5.14.1752358
  5. Prota, G. The chemistry of melanins and melanogenesis. Fortschr. Chem. Org. Naturst 64: 93-148, 1995
  6. Slominski, A., Tobin, D.J., Shibahara, S., Wortsman, J. Melanin pigmentation in mammalian skin and its hormonal regulation. Physiol. Rev. 84: 1155-1228, 2004 https://doi.org/10.1152/physrev.00044.2003
  7. Kobayashi, T., Imokawa, G., Bennett, D.C., Hearing, V.J. Tyrosinase stabilizaton by Tyrp1 (the brown locus protein). J. Biol. Chem 273: 31801-31805, 1998 https://doi.org/10.1074/jbc.273.48.31801
  8. Manga, P., Sato, K., Ye, L., Beermann, F., Lamoreux, M.L., Orlow, S.J. Mutational analysis of the modulation of tyrosinase by tyrosinase-related protein 1 and 2 in vitro. Pigment Cell Res 13: 364-374, 2000 https://doi.org/10.1034/j.1600-0749.2000.130510.x
  9. Tsatmali, M., Ancans, J., Thody, A.J. Melanocyte function and its control by melanocortin peptides. J. Histochem. Cytochem 50: 125-133, 2002 https://doi.org/10.1177/002215540205000201
  10. No, J.K., Soung, D.Y., Kim, Y.J., Shim, K.H., Jun, Y.S., Rhee, S.H., Yokozawa, T., Chung, H.Y. Inhibition of tyrosinase by green tea components. Life Sci. 65: 241-246, 1999
  11. Martinez-Esparza, M., Jimenez-Cervantes, C., Solano, F., Lozano, J.A., Garcia-Borron, J.C. Mechanisms of melanogenesis inhibition by tumor necrosis factor-alpha in B16/F10 mouse melanoma cells. Eur. J. Biochem 255: 139-146, 1998 https://doi.org/10.1046/j.1432-1327.1998.2550139.x
  12. Post, P.W., Daniels, F., Binford, R.T. Cold injury and the evolution of white skin. Hum. Biol 47: 65-80, 1975
  13. Smalley, K., Eisen, T. The involvement of p38 mitogen- activated protein kinase in the $\alpha$-melanocyte stimulating hormone ($\alpha$-MSH)-induced melanogenic and anti-proliferative effects in B16 murine melanoma cells. FEBS Lett 476: 198-202, 2000 https://doi.org/10.1016/S0014-5793(00)01726-9
  14. Widlund, H.R., Fisher, D.E. Microphthalamia-associated transcription factor: a critical regulator of pigment cell development and survival. Oncogene 22: 3035-3041, 2003 https://doi.org/10.1038/sj.onc.1206443
  15. Abdel-Malek, Z., Suzuki, I., Tada, A., Im, S., Akcali, C. The melanocortin-1 receptor and human pigmentation. Ann. N. Y. Acad. Sci 885: 117-133, 1999 https://doi.org/10.1111/j.1749-6632.1999.tb08669.x