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Beauty Food Activities of Isolated Phenolic Compounds from Tetragonia tetragonioides

번행초(Tetragonia tetragonioides)로부터 추출한 Phenolic Compounds의 미용 식품 활성

  • Jo, Jae-Bum (School of Food Science & Biotechnology/Food & Bio-Industry Research Institute, Kyungpook National University) ;
  • Lee, Eun-Ho (School of Food Science & Biotechnology/Food & Bio-Industry Research Institute, Kyungpook National University) ;
  • Cho, Young-Je (School of Food Science & Biotechnology/Food & Bio-Industry Research Institute, Kyungpook National University)
  • 조재범 (경북대학교 식품공학부/식품생물연구소) ;
  • 이은호 (경북대학교 식품공학부/식품생물연구소) ;
  • 조영제 (경북대학교 식품공학부/식품생물연구소)
  • Received : 2015.09.09
  • Accepted : 2016.01.25
  • Published : 2016.03.31

Abstract

This study examined the beauty food activities of water and ethanol extracts from Tetragonia tetragonioides. Content of phenolic compounds extracted with water and 50% ethanol extracts were 3.29 mg/g and 4.14 mg/g, respectively. 1,1-Diphenyl-2-picrylhydrazyl free radical scavenging activities of water and ethanol extracts were 98.45% and 91.20%, respectively, at $200{\mu}g/mL$ of phenolics. 2,2'-Azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) radical decolorization activity was 97.28% for water extracts and 97.83% for ethanol extracts at $100{\mu}g/mL$ of phenolics. Antioxidant protection factor (PF) was 1.77 PF for water and ethanol extracts at $200{\mu}g/mL$ of phenolics. Thiobarbituric acid reactive substances of water and ethanol extracts were 94.77% and 95.64%, respectively, at $100{\mu}g/mL$ of phenolics. Tyrosinase inhibitory activity, which is related to skin-whitening, was confirmed to be 34.96% for ethanol extracts at $200{\mu}g/mL$ of phenolics. Elastase inhibitory activity and anti-wrinkle effect of 50% ethanol extracts were 78.9% at $200{\mu}g/mL$ of phenolics. Collagenase inhibitory activity of ethanol extracts was 61.29% at $200{\mu}g/mL$ of phenolics. Astringent effect was not detected in water extracts but was 7.82% for 50% ethanol extracts at $200{\mu}g/mL$ of phenolics. Hyaluronidase inhibitory activity as a measure of anti-inflammation was confirmed to be 81.04% for water extracts at $200{\mu}g/mL$ of phenolics. Based on these results, Tetragonia tetragonioides extracts can be used as a functional material and functional beauty food with antioxidant effects.

본 연구는 물과 ethanol을 추출용매로 사용한 번행초(Tetragonia tetragonioides) 추출물이 미용 식품 소재로 사용 가능한 기능성을 증명하고자 하였다. Phenolic compounds는 물 추출물에서 3.29 mg/g, 50% ethanol 추출물에서 4.14 mg/g의 결과를 각각 나타내었다. 전자공여능 측정 결과 $200{\mu}g/mL$ phenolic compounds의 농도에서 물 추출물은 98.45%, 50% ethanol 추출물은 91.20%의 활성을 나타내었다. ABTS radical 활성 측정 결과 $100{\mu}g/mL$ phenolic compounds의 농도에서 물 추출물은 97.28%, 50% ethanol 추출물은 97.03%의 활성을 나타내었다. Antioxidant protection factor(PF) 측정 결과 $200{\mu}g/mL$ phenolic compounds의 농도에서 물과 ethanol 추출물 모두 1.77 PF의 같은 결과를 나타내었다. Thiobarbituric acid reactive substance(TBARS) 측정 결과 $100{\mu}g/mL$ phenolic compounds의 농도에서 물과 ethanol 추출물은 94.77%와 95.64%의 높은 활성을 나타내었다. 미백과 관련 있는 tyrosinase 저해 활성을 측정한 결과 $200{\mu}g/mL$ phenolic compounds의 농도에서 ethanol 추출물은 34.96%의 억제력을 나타내었다. 주름 개선 효과를 측정하는 elastase 저해 활성과 collagenase 저해 활성을 측정한 결과 $200{\mu}g/mL$ phenolic compounds의 농도에서 ethanol 추출물만 78.90%와 61.3%의 높은 저해 활성을 나타내었다. 수렴 효과를 나타내는 astringent effect에서 $200{\mu}g/mL$ phenolic compounds 농도의 ethanol 추출물은 7.82%의 효과를 나타내었다. Hyaluronidase 저해 효과 측정 결과 물 추출물 $200{\mu}g/mL$ phenolic compounds의 농도에서 81.04%의 염증 억제 효과를 나타내었다. 이러한 결과들로 미루어 보았을 때 번행초 추출물은 항산화 작용과 미용 식품으로서의 기능성을 기대할 수 있다.

Keywords

References

  1. Oh KH. 2010. Study on the satisfaction and purchasing behaviors in users of DIY natural cosmetics. MS Thesis. Sookmyung Women's University, Seoul, Korea. p 1-93.
  2. Cho YJ. 2011. Characteristics of cosmetic with whitening compounds from Phellodendron amurense. J Appl Biol Chem 54: 108-113. https://doi.org/10.3839/jabc.2011.019
  3. Cho YJ, An BJ, Kim JH. 2011. Application of isolated tyrosinase inhibitory compounds from persimmon leaves. J Life Sci 21: 976-984. https://doi.org/10.5352/JLS.2011.21.7.976
  4. Lee TB. 1978. Illustrated flora of Korea. Hyangmunsa, Seoul, Korea. p 323.
  5. Shin MK. 1986. Clinical galenic pharmacy. Youngrimsa, Seoul, Korea. p 338-339.
  6. National Chinese Medicine Administration Chinese Materia Medica Editorial Board. 1999. Chinese materia medica. Shanghai Science and Technology Publisher, Shanghai, China. p 1391.
  7. New Jiangsu Medical Center. 1998. Dictionary of Chinese medicine. Shanghai Science and Technology Publisher, Shanghai, China. p 2280-2281.
  8. Kato M, Takeda T, Ogihara Y, Shimizu Mm, Nomura T, Tomita T. 1985. Studies on the structure of polysaccharide from Tetragonia tetragonoides. I. Chem Pharm Bull 33: 3675-3680. https://doi.org/10.1248/cpb.33.3675
  9. Singh NP, Schmidt RR. 1989. Synthesis of a (4E,8Z)-sphingadienine moiety containing cerebroside from Tetragonia tetragonoides with antiulcerogenic activity. J Carbohydr Chem 8: 199-216. https://doi.org/10.1080/07328308908048004
  10. Aoki T, Takagi K, Hirata T, Suga T. 1982. Two naturally occurring acyclic diterpene and norditerpene aldehydes from Tetragonia tetragonioides. Phytochemistry 21: 1361-1363. https://doi.org/10.1016/0031-9422(82)80142-8
  11. Cambie RC, Ferguson LR. 2003. Potential functional foods in the traditional Maori diet. Mutat Res 523-524: 109-117. https://doi.org/10.1016/S0027-5107(02)00344-5
  12. Okuyama E, Yamazaki M. 1983. The principles of Tetragonia tetragonioides having anti-ulcergenic activity. I. Isolation and identification of a sterol glucoside mixture (compound A). Yakugaku Zasshi 103: 43-48. https://doi.org/10.1248/yakushi1947.103.1_43
  13. Kemp MS, Burden RS, Brown C. 1979. A new naturally occurring flavanone from Tetragonia expansa. Phytochemistry 18: 1765-1766. https://doi.org/10.1016/0031-9422(79)80215-0
  14. Mori K, Kinsho T. 1988. Synthesis of sphingosine relatives, VII. Synthesis of anti-ulcerogenic cerebrosides isolated from Tetragonia tetragonoides. Liebigs Ann Chem 1988: 807-814. https://doi.org/10.1002/jlac.198819880818
  15. Bar T, Schmidt RR. 1988. Glycosyl imidates, 35. Synthesis of a cerebroside having a (4E,8E)-sphingadienine moiety from Tetragonia tetragonioides with antiulcerogenic activity. Liebigs Ann Chem 1988: 669-674. https://doi.org/10.1002/jlac.198819880709
  16. Chung AK. 2003. Phenolic constituents from Tetragonia tetragonoides. Sungkyunkwan University, Seoul, Korea. p 18-19.
  17. Folin O, Denis W. 1912. On phosphotungstic-phosphomolybdic compounds as color reagents. J Biol Chem 12: 239-249.
  18. Blois MS. 1958. Antioxidant determinations by the use of a stable free radical. Nature 181: 1199-1200. https://doi.org/10.1038/1811199a0
  19. Pellegrin N, Roberta R, Min Y, Catherine RE. 1998. Screening of dietary carotenoids and carotenoid-rich fruit extracts for antioxidant activities applying 2,2'-azinobis(3- ethylenebenzothiazoline-6-sulfonic acid) radical cation decolorization assay. Method Enzymol 299: 379-389.
  20. Andarwulan N, Shetty K. 1999. Phenolic content in differentiated tissue cultures of untransformed and Agrobacterium- transformed roots of anise (Pimpinella anisum L.). J Agric Food Chem 47: 1776-1780. https://doi.org/10.1021/jf981214r
  21. Buege JA, Aust SD. 1978. Microsomal lipid peroxidation. Method Enzymol 52: 302-310. https://doi.org/10.1016/S0076-6879(78)52032-6
  22. Kraunsoe JA, Claridge TD, Lowe G. 1996. Inhibition of human leukocyte and porcine pancreatic elastase by homologues of bovine pancreatic trypsin inhibitor. Biochemistry 35: 9090-9096. https://doi.org/10.1021/bi953013b
  23. Wunsch E, Heidrich HG. 1963. Zur quantitativen bestimmung der kollagenase. Hoppe-Seylers Z Physiol Chem 333: 149-151. https://doi.org/10.1515/bchm2.1963.333.1.149
  24. Hearing VJ Jr. 1987. Mammalian monophenol monooxygenase (tyrosinase): purification, properties, and reactions catalyzed. Methods Enzymol 142: 154-165. https://doi.org/10.1016/S0076-6879(87)42024-7
  25. Lee JT, Jeong YS, An BJ. 2002. Physiological activity of Salicornia herbacea and its application for cosmetic materials. Kor J Herbology 17: 51-60.
  26. Reissig JL, Storminger JL, Leloir LF. 1995. A modified colorimetric method for the estimation of N-acetylamino sugars. J Biol Chem 217: 959-966.
  27. Choi Y, Kim M, Shin JJ, Pack JM, Lee J. 2003. The antioxidant activities of the some commercial teas. J Korean Soc Food Sci Nutr 32: 723-727. https://doi.org/10.3746/jkfn.2003.32.5.723
  28. Kim SM, Cho YS, Sung SK. 2001. The antioxidant ability and nitrite scavenging ability of plant extracts. Korean J Food Sci Technol 33: 626-632.
  29. Kim MK, Jeong CS, Shin YK, Park KH, Lee WJ, Lee EJ, Park KY. 2010. Effects of extraction condition on extraction efficiency of rubiadin in adventitious roots of noni (Morinda citrifolia). Kor J Hort Sci Technol 28: 685-690.
  30. Lee MA, Choi HJ, Kang JS, Choi YW, Joo WH. 2008. Antioxidant activities of the solvent extracts from Tetragonia tetragonioides. J Life Sci 18: 220-227. https://doi.org/10.5352/JLS.2008.18.2.220
  31. Kyu JM. 2010. Monitoring the changes of 2,2-diphenyl- 1-picrylhydrazyl (DPPH) absorbance and oxidation products in thermally oxidized linoleic acid. MS Thesis. Seoul National University, Seoul, Korea. p 24.
  32. Ha GJ, Jeong CH, Jeong HR, Heo HJ, Shon GM, Rho CW, Kim NK. 2011. Antioxidant activities from the different parts of Artemisia argyi H. using an in vitro system. J Agric Life Sci 45: 109-117.
  33. Kim C, In MJ, Kim DC. 2015. In vitro antioxidant activity of ethanol extract from Boehmeria nivea L. leaves. Food Eng Prog 19: 76-81. https://doi.org/10.13050/foodengprog.2015.19.1.76
  34. Ratnam DV, Ankola DD, Bhardwaj V, Sahana DK, Kumar MN. 2006. Role of antioxidants in prophylaxis and therapy: A pharmaceutical perspective. J Control Release 113: 189-207. https://doi.org/10.1016/j.jconrel.2006.04.015
  35. Sies H. 1997. Oxidative stress: oxidants and antioxidants. Exp Physiol 82: 291-296. https://doi.org/10.1113/expphysiol.1997.sp004024
  36. Beckman KB, Ames BN. 1998. The free radical theory of aging matures. Physiol Rev 78: 547-581. https://doi.org/10.1152/physrev.1998.78.2.547
  37. Cha JY, Lee SJ, Shin JH, Sung NJ. 2012. Antioxidant and inhibition of nitrosodimethylamine formation in marketing black garlics. J Agric Life Sci 46: 151-162.
  38. Shon MY. 2007. Antioxidant and anticancer activities of Poria cocos and Machilus thunbergii fermented with mycelial mushrooms. Food Industry and Nutrition 12(2): 51-57.
  39. Choi JH, Kim JH, Jung JY, Suh SG. 2013. Comparison of nerve growth factor induction and anti-aging activity using dried Gastrodia and fermented Gastrodia extracts. Kor J Hort Sci Technol 31: 380-387.
  40. Kim JW, Lee SH, No HK, Hong JH. 2010. Antioxidant properties of cultured wild ginseng roots extracts. Korean J Food Preserv 17: 861-866.
  41. Vinson JA, Su X, Zubik L, Bose P. 2001. Phenol antioxidant quantity and quality in foods: fruits. J Agric Food Chem 49: 5315-5321. https://doi.org/10.1021/jf0009293
  42. Tsukahara K, Nakagawa H, Moriwaki S, Takema Y, Fujimura T, Imokawa G. 2006. IInhibition of ultraviolet-B-induced wrinkle formation by an elastase-inhibiting herbal extract: implication for the mechanism underlying elastase-associated wrinkles. Int J Dermatol 45: 460-468. https://doi.org/10.1111/j.1365-4632.2006.02557.x
  43. Kim DM, Kim KH, Kim YS, Koh JH, Lee KH, Yook HS. 2012. A study on the development of cosmetic materials using unripe peaches seed extracts. J Korean Soc Food Sci Nutr 41: 110-115. https://doi.org/10.3746/jkfn.2012.41.1.110
  44. Cho EK, Choi YJ. 2010. Physiological activities of hot water extracts from Ecklonia cava Kjellman. J Life Sci 20: 1675-1682. https://doi.org/10.5352/JLS.2010.20.11.1675
  45. Kim KB, Jo BS, Lee JY, Park KT, An BJ, Lee SH, Cho YJ. 2012. Beauty food activities of isolated phenolic compounds from Ulmus pumila. J Appl Biol Chem 55: 207-215. https://doi.org/10.3839/jabc.2012.033
  46. Perlish JS, Lemlich G, Fleischmajer R. 1998. Identification of collagen fibrils in scleroderma skin. J Invest Dermatol 90: 48-54.
  47. El-Domyati M, Attia S, Saleh F, Brown D, Birk DE, Gasparro F, Ahmad H, Uitto J. 2002. Intrinsic aging vs. photoaging: a comparative histopathological, immunohistochemical, and ultrastructural study of skin. Exp Dermatol 11: 398-405. https://doi.org/10.1034/j.1600-0625.2002.110502.x
  48. Wlaschek M, Tantcheva-Poor I, Naderi L, Ma W, Schneider LA, Razi-Wolf Z, Schuller J, Scharffetter-Kochanek K. 2001. Solar UV irradiation and dermal photoaging. J Photochem Photobiol B 63: 41-51. https://doi.org/10.1016/S1011-1344(01)00201-9
  49. Lee BG, Kim JH, Ham SG, Lee CE. 2014. Study on biological activities of extracts for cosmeceutical development from Lagerstroemia indica L. branch. Korean J Plant Res 27: 29-34. https://doi.org/10.7732/kjpr.2014.27.1.029
  50. Lee YS, Kim BO, Kim NW. 2014. Anti-wrinkle and antioxidant activity of the extract of Albizzia julibrissin leaves. J Invest Cosmetol 10: 317-326. https://doi.org/10.15810/jic.2014.10.4.009
  51. Tsuji N, Moriwaki S, Suzuki Y, Takema Y, Imokawa G. 2001. The role of elastases secreted by fibroblasts in wrinkle formation: implication through selective inhibition of elastase activity. Photochem Photobiol 74: 283-290. https://doi.org/10.1562/0031-8655(2001)074<0283:TROESB>2.0.CO;2
  52. Jee SO. 2009. Antioxidant activities and whitening effect of the mulberry (Morus alba L.) root bark extracts. Korean J Plant Res 22: 145-151.
  53. Lee YS, Choi JB, Joo EY, Kim NW. 2007. Antioxidative activities and tyrosinase inhibition of water extracts from Ailanthus altissima. J Korean Soc Food Sci Nutr 36: 1113-1119. https://doi.org/10.3746/jkfn.2007.36.9.1113
  54. Roth GJ, Siok CJ, Ozols J. 1980. Structural characteristics of prostaglandin synthetase from sheep vesicular gland. J Biol Chem 255: 1301-1304.
  55. DeWitt DL, Rollins TE, Day JS, Gauger JA, Smith WL. 1981. Orientation of the active site and antigenic determinants of prostaglandin endoperoxide synthase in the endoplasmic reticulum. J Biol Chem 256: 10375-10382.
  56. Youn JS, Shin SY, Wu Y, Hwang JY, Cho JH, Ha YG, Kim JK, Park MJ, Lee S, Kim TH, Kim TW. 2012. Antioxidant and anti-wrinkling effects of Aruncus dioicus var. kamtschaticus extract. Korean J Food Preserv 19: 393-399. https://doi.org/10.11002/kjfp.2012.19.3.393
  57. Lee SY, Jun HJ, Yoon JY, Kim TS, Park S, Lee SP, Park JH, Lee JY. 2012. Cosmeceutical activity of broccoli (Brassica oleracea var. italica Plenck) with different light sources. J Life Sci 22: 347-353. https://doi.org/10.5352/JLS.2012.22.3.347
  58. Kim JS, Lee JY, Park KT, An BJ, Lee SH, Cho YJ. 2013. The biological activity from Prunella vulgaris extracts. Korean J Food Preserv 20: 234-241. https://doi.org/10.11002/kjfp.2013.20.2.234
  59. Cho YJ, AN BJ. 2008. Anti-inflammatory effect of extracts from Cheongmoknosang (Morus alba L.) in lipopolysaccharide- stimulated raw cells. J Korean Soc Appl Biol Chem 51: 44-48.
  60. Ghosh P. 1994. The role of hyaluronic acid (hyaluronan) in health and disease: interactions with cells, cartilage and components of synovial fluid. Clin Exp Rheumatol 12: 75-82.
  61. Cha BC, Lee EH. 2004. Antioxidant and antiinflammation activities of Prunus persica tree extracts. Korean J Med Crop Sci 12: 289-294.
  62. Kim HH, Park GH, Park KS, Lee JY, An BJ. 2010. Anti-oxidant and anti-inflammation activity of fractions from Aster glehni Fr. Schm. Kor J Microbiol Biotechnol 38: 434-441.
  63. Choi HJ, Shim SB, Kim NJ, Kim JW. 1988. Studies on the efficacies of water extract of propolis. J Appl Pharmacol 6: 261-268.

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