DOI QR코드

DOI QR Code

Effect of Sorghum nervosum extract on an anti-inflammatory and cytoprotective

고량(Sorghum nervosum)추출물의 항염증 및 세포 보호 효과

  • Lee, Ju-Hyun (Department of Bioengineering, Konkuk University) ;
  • Kim, Kum-Lan (Department of Doowon Technical University, Gyeonggi Industrial Technical Education Center) ;
  • Moon, Ji-sun (Department of Beauty Health, Jungwon University)
  • 이주현 (건국대학교 생물공학과) ;
  • 김금란 (두원공과대학교 경기 산업기술 교육센터) ;
  • 문지선 (중원대학교 뷰티헬스학과)
  • Received : 2017.08.02
  • Accepted : 2017.09.03
  • Published : 2017.09.30

Abstract

This study was intended to test anti-inflammation and cytoprotective effect against UVB after Sorghum nervosum was extracted with 70% ethanol. The efficacy of Sorghum nervosum was assessed regarding cell viability analysis, reactive oxygen species measurement, anti-inflammation, a change in COX-2 protein, and cytoprotective effect against UVB. According to the results of experiment, the cell viability of 97% or higher was shown at all concentrations of Sorghum nervosum in RAW264.7 macrophage, HaCaT cell. And in anti-inflammatory NO inhibitory activity, a concentration-dependent inhibitory effect was shown. And COX-2 protein expression was also significantly (p<.001) inhibited at 25, $50{\mu}g/mL$. With regard to cytoprotective effect against UVB, in the quantitative analysis results of reactive oxygen species within the cell, it was verified that Sorghum nervosum extract had an effect on an decrease in the total amount of ROS. When the results of study are considered comprehensively, it is thought that there is possibility of Sorghum nervosum development as raw materials for cosmetics showing an anti-inflammation and cytoprotective function against UVB.

본 연구에서는 고량(Sorghum nervosum) 70 % 에탄올 추출 후 항염증 및 UVB에 대한 세포 보호 효과를 검증하고자 하였다. 고량 추출물의 효능 평가는 세포생존율분석, 활성산소 측정, 항염증, COX-2 단백질 변화, UVB에 대한 세포 보호 효과를 수행하였다. 실험 결과, RAW264.7 대식세포, HaCaT 세포에서 고량추출물 모든 농도에서 97 %이상 세포 생존율을 확인하였다. 항염증 NO 생성 억제능에서는 농도 의존적으로 저해 효과가 나타났으며, COX-2 단백질 발현량 역시 25, $50{\mu}g/mL$ 농도에서 유의하게(p<.001) 저해되었다. UVB에 대한 세포 보호 효과로는 세포 내 활성산소종(ROS) 정량 분석 결과, 고량 추출물이 ROS 총 양 감소에 효과가 있음을 확인하였다. 연구결과를 종합적으로 고려해 볼 때, 고량추출물은 항염증 및 UVB에 대한 세포 보호 기능을 나타내는 화장품 원료로서의 개발 가능성이 있다고 사료된다.

Keywords

References

  1. Chandra J, Samali A, Orrenius S. "Triggering and modulation of apoptosis by oxidative stress", Free Radic Biol Med. vol. 29, pp. 323-333, (2000). https://doi.org/10.1016/S0891-5849(00)00302-6
  2. Buttke TM, Sandstrom PA. "Oxidative stress as a mediator of apoptosis", Immunol Today. vol. 15, pp. 7-10, (1994). https://doi.org/10.1016/0167-5699(94)90018-3
  3. Fang J, Nakamura H, Iyer AK. "Tumortargeted induction of oxystress for cancer therapy". J. Drug Target. vol. 15, pp. 475-486, (2007). https://doi.org/10.1080/10611860701498286
  4. Barbouti A, Doulias PT, Nousis L, Tenopoulou M, Galaris D. "DNA damage and apoptosis in hydrogen peroxideexposed Jurkat cells: bolus addition versus continuous generation of H2O2", Free Radical Biology & Medicine, vol. 33,vol. 691-702, (2002). https://doi.org/10.1016/S0891-5849(02)00967-X
  5. Nathan CF. "Secretory products of macrophages", The Journal of Clinical Investigation, vol. 79, pp. 319-326, (1987). https://doi.org/10.1172/JCI112815
  6. Burns ER. "Methods for estimation of tannin in grain sorghum", Agronomy Journal. vol. 63, pp. 511-514, (1971). https://doi.org/10.2134/agronj1971.00021962006300030050x
  7. Nip WK, Burns EE. "Pigment charaterization in grain sorghum I Red varieties. Cereal Chemistry, vol. 46, pp. 490-495, (1969).
  8. Awika JM, Rooney LW, Wu X, Prior RL, Cisneros-Zevallos L. "Screening methods to measure antioxidant activity of sorghum(sorghum bicolor) and sorghum products", Journal of Agricultural and Food Chemistry. vol. 51, pp. 6657-6662, (2003). https://doi.org/10.1021/jf034790i
  9. Gupta RK, Haslam E. "Plant proanthocyanidins", Journal of Chemical Society. vol. 8 pp. 892-896, (1978).
  10. Gu L, Keim M, Hammersone JF, Beecher G, Cunningham D, Vannozzi S, Prior L. "Fractionation of polymeric procyanidins from lowbush blueberry and quantification of procyanidins in slscted foods with an optimized normal phase HPLC-MS fluorescent detection method", Journal of Agricultural and Food Chemistry. vol. 50, pp.4852-4860. (2002). https://doi.org/10.1021/jf020214v
  11. Kim JS. "Dyeing Power of Coating Permanent to Utilize a Kaoliang Pigment", Kor. J. Aesthet. Cosmetol., vol. 12, pp. 127-132, (2014).
  12. Kandaswami C, Middleton JE. "Free radical scavenging and antioxidant activity of plant flavonoids", Adv. Exp. Med. Biol., vol. 366, pp. 351-376, (1994).
  13. Rice-Evans CA, Miller NJ. "Antioxidant activities of flavonoids as bioactive components of food", Biochem. Soc. Trans., vol. 24, pp. 790-795, (1996). https://doi.org/10.1042/bst0240790
  14. Robak J, Shridi F, Wolbis M, and Krolikowska M. "Screening of the influence of flavonoids on lipoxygenase and cyclooxygenase activity, as well as on nonenzymic lipid oxidation", Pol. J. Pharmacol. Pharm., vol. 40, pp. 451-458, (1998.)
  15. Oh KN, "Protective effects of apigenin and luteolin on ultraviolet A-induced Matrix Metalloproteinase expression in human keratinocyts", Department of Pharmacy, Graduate School of Chosun University, (2007).
  16. Sreemanti D, Jayeeta D, Avijit P, Asmita S, Anisur RK. "Apigenin, a bioactive flavonoid from Lycopodium clacatum, stimulates nucleotide excision repair genes to protect skin keratinocytes from ultraviolet B-induced reactive oxygen species and DNA damage", J. Acupunct. Meridian Stud., vol. 6, pp. 252-262, (2013). https://doi.org/10.1016/j.jams.2013.07.002
  17. Robak J, Shridi F, Wolbis M, and Krolikowska M. "Screening of the influence of flavonoids on lipoxygenase and cyclooxygenase activity, as well as on nonenzymic lipid oxidation", Pol. J. Pharmacol. Pharm., vol. 40, pp. 451-458, (1998).
  18. Borenfreund E, Puerner JA, "Toxicity determined in vitro by morphologica lalterationsandneutra lred absorption", Toxicol.Lett., vol. 24, pp. 119, (1985). https://doi.org/10.1016/0378-4274(85)90046-3
  19. Green LC, Wagner DA, Glogowski J, Skippr PL, Wishnok JS, "Tannenbaum SR. Analysis of nitrate, nitrite, and [15N] nitrate in biological fluids", Anal Biochem., vol. 126, pp. 131-138, (1982). https://doi.org/10.1016/0003-2697(82)90118-X
  20. Borenfreund E, Puerner JA. "Toxicity determined in vitro by morphological alterations and neutral red absorption", Toxicol Lett., vol. 24, pp. 119-124, (1984).
  21. Miliani de Marval PL, Zhang Y. "The RP-Mdm2-p53 pathway and tumorigenesis", Oncotarget., vol. 2, pp. 234-238, (2011).
  22. Seibert K, Zhang Y, Leahy K, Hauser S, Masferrer J, Perkins W. "Pharmacological and biochemical demonstration of the role of cyclooxygenase 2 in inflammation and pain", Proc. Natl. Acad. Sci. USA, vol. 91, pp. 12013-12017, (1994). https://doi.org/10.1073/pnas.91.25.12013
  23. Levy GN. "Prostaglandin H synthases, nonsteroidal anti-inflammatory drugs, and colon cancer", FASEB. J, vol. 11, pp. 234-247, (1997). https://doi.org/10.1096/fasebj.11.4.9068612
  24. Takahashi M, Mutoh M, Shoji Y, Sato H, Kamanaka Y, Naka M, Mar uyama T, Sugimura T, Wakabayashi K. "Suppressive effect of an inducible nitric oxide inhibitor, ONO-1714, on AOM-induced rat clon carcinogenesis", Nitric Oxide, vol. 14, pp. 130-136, (2006). https://doi.org/10.1016/j.niox.2005.07.004
  25. Xie W, Chpman JG, Robertson DL, Erikson RL, Simmons DL. "Expression of a Mitogen-responsive Gene Encoding Prostaglandin Synthetase in Regulated by mRNA Splicing", Proc. Natl. Acad. Sci. USA, vol. 88, pp. 2692-2696, (1991). https://doi.org/10.1073/pnas.88.7.2692
  26. Kujubu DA, Fletcher BS, Varnum BC, Lim Rw, Herschman HR. "TIS10, a Phorbol Ester Tumor Promoter-inducible mRNA from Swiss 3T3 cells, Encodes a Novel Prostaglandin Synthase/Cyclooxygenase Homologue", J. Biol. Chem, vol. 266, pp. 12866-12938, (1991).
  27. O'Banion MK, Sadowski HB, Winn V, Young DA. "A Serum and Glucocorticoid Regulated 4 Kilobase mRNA Ecodes a Cyclooxygenase Related Protein", J. Biol. Chem, vol. 266, pp. 23261-23267, (1991).
  28. Kenny BP, Chan CC, Culp SA, Cromlish WA. "Cloning and Expression of Rat Prostaglandin Endoperoxide Synthase Cyclooxygenase-2 cDNA", Biophys. Res. Commun, vol. 197, pp. 494-500, (1993). https://doi.org/10.1006/bbrc.1993.2506
  29. Vane JR, Mitchell JA, Appleton I, Tomlinson A, Bishop Bailey D, Crotall J, Willoughby DA. "Inducible Isoforms of Cyclooxygenase and Nitric Oxide Synthase in Inflammation", Proc Natl Acad Sci USA, vol. 91, pp. 2046-2050, (1994). https://doi.org/10.1073/pnas.91.6.2046
  30. Massferrer JL, Zweifel BS, Manning PT, Hauser SD, Leahy KM, Smith WG, Isakson PC, Seibert K. "Selective Inhibition of Inducible Cyclooxygenase-2 in vivo is Antiinflammatory and Nonulcerogenic", Proc. Natl. Acad. Sci. USA, vol. 91, pp. 3228-3232, (1994). https://doi.org/10.1073/pnas.91.8.3228