Antioxidative and Anti-inflammatory Effects of Petasites japonicus

머위추출물의 항산화와 항염증 효과

  • 김진화 (한불화장품(주) 기술연구소) ;
  • 나영 (한불화장품(주) 기술연구소) ;
  • 심관섭 (한불화장품(주) 기술연구소) ;
  • 이범천 (한불화장품(주) 기술연구소) ;
  • 표형배 (한불화장품(주) 기술연구소)
  • Published : 2006.12.30

Abstract

Antioxidative and anti-inflammatory activities of Petasites japonicus extract were evaluated. P. japonicus extract showed 70.1% inhibition on peroxidation of linoleic acid. In the experiment using the cell permeable dye, 2',7'- dichlorofluorescein diacetate (DCFDA) as an indicator of reactive oxygen species (ROS) generation, intracellular oxidative stress in UVB-irradiated keratinocytes was shown to be decreased by P. japonicus extract. Also, UVB-induced production of interleukin-$1{\alpha}$ and prostaglandin $E_2$ in human HaCaT keratinocytes was reduced in a dose-dependent manner by treatment with P. japonicus extract. All these results suggest that P. japonicus extract can be effectively used for prevention of UV-induced adverse skin reactions such as radical production and inflammation.

태양광선과 산소는 피부세포에 자유라디칼(free radical)과 활성산소종(reactive oxygen species, ROS)을 생성시켜 세포막 지질의 과산화와 염증을 유발한다. 본 연구는 자외선에 의한 피부손상에 대한 머위추물물의 피부 보호효과에 대한 것으로 UVB가 조사된 각질형성세포에서이 항산화 및 염증관련 사이토카인의 억제효과를 측정하였다. 라디칼에 의한 지질과산화에 대한 억제효과는 $100{\mu}g/mL$에서 70.1%로 우수하게 나타났으며, 세포내에서 ROS에 의해 형광을 띠는 물질로 전환되는 $CM-H_2DCFDA$를 이용하여 ROS의 양을 측정한 결과 자외선에 의해 증가된 세포내 ROS의 양이 머위추출물을 처리함으로써 $500{\mu}g/mL$ 농도에서 45% 이상의 우수한 소거효과를 나타냈다. 또한 각질형성세포에서 UVB에 의해 생합성이 증가되는 $IL-1{\alpha}$$PGE_2$의 생합성 억제효과는 $100{\mu}g/mL$에서 각각 25.7%, 59.3%를 저해하는 것으로 우수한 효과를 나타내었다. 따라서 머위추출물은 각질형성세포에서 자외선 조사에 의한 피부손상에 대한 보호효과를 가진 화장품에서 우수한 소재로 적용될 수 있다.

Keywords

References

  1. B. N. Ames, M. K. Shigenaga, and T. M. Hagen, Oxidants, antioxidants, and the degenerative disease of aging, Proc. Natl. Sci. USA, 90, 7915 (1993)
  2. D. Dreher and A. F. Junod, Role of oxygen free radicals in cancer development, Eur. J. cancer, 32A, 30 (1998)
  3. B. Halliwell, J. M. C. Gutteridge, and C. E. Cross, Free radicals, antioxidants, and human disease: where are we now-, J. Lab. Clin. Med, 119, 598 (1992)
  4. A. J. Dannenberg, N. K. Altorki, J. O. Boyle, C. Dang, L. R. Howe, B. B. Weksler, and K. Subbaramaiah, Cyclooxygenase-2; a pharmacological target for the prevention of cancer, Lancet Oncol., 2, 544 (2001) https://doi.org/10.1016/S1470-2045(01)00488-0
  5. M. Tsujii, S. Kawano, S. Tsujii, H. Sawaoka, M. Hori, and R. N. Dubois, Cyclooxygenase regulates angiogenesis induced by colon cancer cells, Cell, 93, 705 (1998) https://doi.org/10.1016/S0092-8674(00)81433-6
  6. H. Sheng, H. Shao, J. D. Morrow, R. D. Beachamp, and R. N. Dubois, Modulation of apoptosis and Bcl-2 expression by prostaglandin E2 in human colon cancer cells, Cancer Res., 58, 362 (1998)
  7. T. Soka, In Dictionary of Chinese Drugs 1st ed. Shanghai Science Technology, Shogakukan Press, Tokyo (1985)
  8. B. S. Min, H. S. Cui, H. K. Lee, D. E. Sok, and M. R. Kim, A new furofuran lignan with antioxidant and anti seizure activities from the leaves of Petasites japonicus, Arch Pharm. Res., 28(9), 1023 (2005) https://doi.org/10.1007/BF02977395
  9. M. H. Bang, Development of biologically activity compound from edible plant sources- XY. Isolation of triterpenoid glycosides from the leaf of Petasites japonicus, J. Korean Soc. Appl. Biol. Chem, 48(4), 421 (2005)
  10. O. B. Choi, Anti-allergic effects of Petasites japonicus, Korean J. Food Nutr., 15, 382 (2002)
  11. C. S. Lee and Y. H, Jee, Pathological changes of rat and mice fed with Petasites japonicus Maxim, Korean J. Vet. Res., 36, 417 (1996)
  12. A. M. Romero, M. M. Dobal, M. A Sturla, and M. A. Judis, Antioxidant properties of polyphenolcontaining extract from soybean fermented with Saccharomyces cerevisia, Eur. J. Lipid Sci. Technol., 106, 424, (2004) https://doi.org/10.1002/ejlt.200400953
  13. S. Y. Seo, E, Y. Kim, H. Kim, and B. J. Gwang, Neuroprotective effect of high glucose against NMDA, free radical and oxygen-glucose deprivation through enhanced mitochondrial potentials, J. Neurosci., 19(20), 8849 (1999)
  14. I. D. Trayner, A. P. Rayner, G. E. Freeamn, and R. Farzaneh, Quantitative multi well myeloid differentiation assay using dichlorcxlihydrofluorescein diacetate ($H_2DCF-DA$) or dihydrorhodamine 123 ($H_2Rl23$), J. Immunological Methods, 186, 275 (1995) https://doi.org/10.1016/0022-1759(95)00152-Z
  15. B. Tebbe, S. Wu, C. C. Geilen, J. Eberle, V. Kodelja, and C. E. Orfanos, L -ascorbic acid inhibits UVA -induced lipid peroxidation and secretion of IL -1 alpha and IL -6 in cultured human keratinocytes in vitro, J. Invest Derm., Vol. 108, 302 (1997) https://doi.org/10.1111/1523-1747.ep12286468