DOI QR코드

DOI QR Code

The chemical constituents, antioxidant activity and anti-inflammatory activities of Solanum nigrum Linne by different harvest time

수확시기별 까마중 전초의 성분, 항산화활성 및 항염증 활성

  • Choi, Seongkyu (Department of Oriental Medicine Resources, Sunchon National University) ;
  • Seo, Kyoung-Sun (Jangheung research institute for mushroom industry) ;
  • Kim, Yong-Doo (Department of Food Science and Technology, Sunchon National University) ;
  • Yun, Kyeong-Won (Department of Oriental Medicine Resources, Sunchon National University) ;
  • Choi, Bong-suk (Jangheung research institute for mushroom industry) ;
  • Jin, Seong-Woo (Jangheung research institute for mushroom industry) ;
  • Kang, Kyeong-Yun (Department of Pharmacy, Sunchon National University) ;
  • Cho, In-Kyung (Jangheung research institute for mushroom industry) ;
  • Kim, Kyung-Je (Jangheung research institute for mushroom industry)
  • 최성규 (순천대학교 한약자원개발학과) ;
  • 서경순 ((재)장흥군버섯산업연구원) ;
  • 김용두 (순천대학교 식품공학과) ;
  • 윤경원 (순천대학교 한약자원개발학과) ;
  • 최봉석 ((재)장흥군버섯산업연구원) ;
  • 진성우 ((재)장흥군버섯산업연구원) ;
  • 강경윤 (순천대학교 약학과) ;
  • 조인경 (남부대학교 식품영양학과) ;
  • 김경제 ((재)장흥군버섯산업연구원)
  • Received : 2016.06.13
  • Accepted : 2016.10.05
  • Published : 2016.11.30

Abstract

In this study, we investigated the variation in free sugars, amino acids, antioxidant activity, and anti-inflammatory activity of Solanum nigrum Linne based on harvest time. Major amino acids identified by HPLC analysis were proline, histidine, and serine. The highest content of total amino acids were found in S. nigrum aerial parts and roots harvested on July 10th and August 10th. Four kinds of free sugars (fructose, glucose, sucrose, maltose) were detected in S. nigrum, and the free sugar content varied significantly with harvest time. The fructose content of S. nigrum decreased with as harvest time increased. The total polyphenol content of S. nigrum was highest in those harvested on August 30th. The antioxidant activity of ethanol extract from S. nigrum collected at different harvest times were measured by DPPH and ABTS radical scavenging assays. The anti-inflammatory activity of these extracts were assayed via nitric oxide suppression in C6 glioma cells with a lipopolysaccharide (LPS)-induced inflammatory response. The anti-inflammatory activity and antioxidant effects were the highest in the extract from S. nigrum collected on August 30th. Good correlations were observed between antioxidant and anti-inflammatory activities in ethanol extract of S. nigrum roots harvested on August 30th.

본 연구는 까마중 수확시기에 따른 성분변화, 항산화효과 및 항염증 효과를 분석하여 최적 수확시기를 구명하고자 수행하였다. 까마중의 주요 아미노산은 수확시기에 관계없이 proline, histidine 과 serine으로 나타났으며, 구성아미노산 함량은 7월 10일과 8월 10일 수확한 까마중 지상부와 지하부에서 높게 나타났다. 4가지 유리당이 검출되었으며, 유리당 함량은 수확시기에 따라 편차를 나타내었다. 유리당 중 fructose는 수확시기가 늦어짐에 따라 감소하였으며, 총 폴리페놀 함량은 8월 30일 수확한 까마중 뿌리에서 가장 높게 나타났다. 수확기별 까마중 ethanol 추출물들의 항산화효과와 항염증효과 검정을 위하여 DPPH radical scavenging assay와 ABTS radical scavenging assay를 수행하였으며, 항염증 효과 측정을 위하여 lipopolysaccharide(LPS)로 염증을 유발시킨 C6 glioma cells을 NO 저해실험에 사용하였다. 항산화효과와 항염증 효과는 8월 30일 수확한 까마중 뿌리 ethanol 추출물에서 가장 높은 활성을 나타내었다. 8월 30일 수확한 까마중 뿌리는 총 폴리페놀 함량, 항산화 효과 및 항염증 효과간의 양적인 상관관계를 나타내었다.

Keywords

References

  1. Euk CS (1997) Flora of medicinal herbs. Kyeongwon Publishing Co, Seoul, Korea, p 80
  2. Lee YN (1997) Korean Flora. Kyohak. Publishing Co, Seoul, Korea, p 700
  3. Yun KY, Kim MY (2010) Flora of Korean medicinal plant. Shinkwang Publishing Co, Seoul, Korea, p 332-333
  4. Huh J 2007 Dong-eu-bo-gam. Bubin Publishing Co, Seoul, Korea, p 1945
  5. Choi SK, Seo KS (2012) Studys on growth charcateristics and yield of Solanum nigrum L. Korean J Plant Res, 25, 596-602 https://doi.org/10.7732/kjpr.2012.25.5.596
  6. Oh SJ, Koh SC (2012) Adventitious shoot formation and plant regeneration from explants of Solanum nigrum L.. Korean J Plant Res, 25, 227-284
  7. Edmonds JM, Chweya JA (1997) Black nightshades, Solanum nigrum L. and related species. International Plant Genetic Resources Institute, Rome, Italy, p 28
  8. Atanu FO, Ebiloma UG, Ajayi EI (2011) A review of the pharmacological aspects of Solanum nigrum Linn.. Biotechnol Mol Biol Rev, 6, 1-7
  9. Joo SY (2013) Antioxidant activities of medicinal plant extracts. J Korean Soc Food Sci Nutr, 42, 512-519 https://doi.org/10.3746/jkfn.2013.42.4.512
  10. Ahn BS, Kim JW, Kim HT, Lee SD, Lee KW (2010) Antioxidant effects of Hovenia Dulcis in the streptozotocininduced diabetic rats. J Vet Clin, 27, 366-373
  11. Tampo Y, Tsukamoto M, Yonaha M (1999) Superoxide production from paraquat evoked by exogenous NADPH in pulmonary endothelial cells. Free Radic Biol Med, 27, 588-595 https://doi.org/10.1016/S0891-5849(99)00110-0
  12. Oh SI, Lee MS (2005) Antioxidative and antimutagenic effects of Ganoderma lucidum Krast extracts. Korean J Food Nutr, 18, 54-62
  13. Kim MJ, Chu WM, Park EJ (2012) Antioxdant and antigenotoxic effects of Shiitake mushrooms affected by different drying methods. J Korean Soc Food Sci Nutr, 41, 1041-1048 https://doi.org/10.3746/jkfn.2012.41.8.1041
  14. Choi Y, Lee SM, Chun J, Lee HB, Lee J (2006) Influence of heat treatment on the antioxidant activities and polyphenolic compounds of Shiitake (Lentinus edodes) mushroom. Food Chem, 99, 381-387 https://doi.org/10.1016/j.foodchem.2005.08.004
  15. Cheung LM, Cheung CK (2005) Mushroom extracts with antioxidant activity against lipid peroxidation. Food Chem, 89, 403-409 https://doi.org/10.1016/j.foodchem.2004.02.049
  16. Wilson AM, Work TM, Bushway AA, Bushway RJ (1981) HPLC determination of fructose, glucose and sucrose in potatoes. J Food Sci, 46, 300-301 https://doi.org/10.1111/j.1365-2621.1981.tb14589.x
  17. Strydom D, Cohen SA (1993) Sensitive analysis of cystine/cysteine using 6-aminoquinolyl-N -hydroxysuccinimidyl carbamate (AQC) derivatives. Tech Protein Chem, 4, 299-306
  18. Velioglu YS, Mazza G, Gao L, Oomah BD (1998) Antioxidant activity and total phenolics in selected fruits, vegetables, and grain products. J Agric Food Chem, 46, 4113-4117 https://doi.org/10.1021/jf9801973
  19. Blois MS (1958) Antioxidant determinations by the use of a stable free radical. Nature, 181, 1199-1200 https://doi.org/10.1038/1811199a0
  20. Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice-Evans C (1999) Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radical Biol Med, 26, 1231-1237 https://doi.org/10.1016/S0891-5849(98)00315-3
  21. Green LC, Wagner DA, Glogowski J, Skipper PL, Wishnok JS, Tannenbaum SR (1982) Analysis of nitrate, nitrite, and [$^{15}N$]nitrate in biological fluids. Anal Biochem, 126, 131-138 https://doi.org/10.1016/0003-2697(82)90118-X
  22. Chang HK (2000) Changes in chemical compositon of Panax ginseng leaves by different harvesting months. Korean J Food Nutr, 13, 6-12
  23. Choi MH, Kang JR, Sim HJ, Kang MJ, Seo WT, Bae WY, Sin JH (2015) Physicochemical characteristics and antioxidant activity of Sumaeyaksuk depending on harvest times and processing methods. Korean J Food Preserv, 22, 399-407 https://doi.org/10.11002/kjfp.2015.22.3.399
  24. Orzechowska B, Janusz M, Domaraczenko B, Blach- Olszewska Z (1998) Antiviral effect of proline-rich polypeptide in murine resident peritoneal cells. Acta Virologica, 42, 75-78
  25. Xie Y, Fleming E, Chen JL, Elmore DE (2011) Effect of proline position on the antimicrobial mechanism of buforin II. Peptides, 32, 677-682 https://doi.org/10.1016/j.peptides.2011.01.010
  26. Eronina TB, Chebotareva NA, Bazhina SG, Makeeva VF, Kleymenov SY, Kurganov BI (2009) Effect of proline on thermal inactivation, denaturation and aggregation of glycogen phosphorylase b from rabbit skeletal muscle. Biophysical Chemistry, 141, 66-74 https://doi.org/10.1016/j.bpc.2008.12.007
  27. Ji Y, Wu Z, Dai Z, Sun K, Wang J, Wu G (2016) Nutritional epigenetics with a focus on amino acids: implications for the development and treatment of metabolic syndrome. J nutrition biochem, 27, 1-8 https://doi.org/10.1016/j.jnutbio.2015.08.003
  28. Semba RD, Shardell M, Sakr Ashour FA, Moaddel R, Trehan I, Maleta KM, Ordiz MI, Kraemer K, Khadeer MA, Ferrucci L, Manary MJ (2016) Child stunting is associated with low circulating essential amino acids. EBioMedicine, 6, 246-252 https://doi.org/10.1016/j.ebiom.2016.02.030
  29. Montesinos Guevara C, Mani AR (2016) The role of D-serine in phripheral tissues. Eur J Pharmacol, 780, 216-223 https://doi.org/10.1016/j.ejphar.2016.03.054
  30. Ferreres F, Gomes D, Valentano P, Goncalves R, Pio R, Chagas EA, Seabra RM, Andrade PB (2009) Improved loquat (Eriobotrya japonica Lindl.) cultivars: variation of phenolics and antioxidantive potential. Food Chem, 114, 1109-1027 https://doi.org/10.1016/j.foodchem.2008.10.065
  31. Wang HC, Chung PJ, Wu CH, Lan KP, Yang MY, Wang CJ (2011) Solanum nigrum L. polyphenolic extract inhibits hepatocarcinoma cell growth by inducing $G_2/M$ phase arrest and apoptosis. J Sci Food Agric, 91, 178-185 https://doi.org/10.1002/jsfa.4170
  32. Jimoh FO, Adedapo AA, Afolayan AJ (2010) Comparison of the nutritional value and biological activities of the acetone, methanol and water extracts of the leaves of Solanum nigrum and Leonotis leonorus. Food Chem Toxicol, 48, 964-971 https://doi.org/10.1016/j.fct.2010.01.007
  33. Jeong HR, Kim JH, Jo YN, Jeong JH, Heo HJ (2011) Characterization as cosmetic substances of chestnut inner skin extracts with antioxidant activity. J Agri Life Sci, 45, 183-191
  34. Georgiev M, Alipieva K, Orhan I, Abrashev R, Denev P, Angelova M (2011) Antioxidant and cholinesterases inhibitory activities of Verbascum xanthophoeniceum Griseb. and its phenylethanoid glycosides. Food Chem, 128, 100-105 https://doi.org/10.1016/j.foodchem.2011.02.083
  35. Lee JH, Jhoo JW (2012) Antioxidant activity of different parts of Lespedeza bicolor and isolation of antioxidant compound. Korean J Food Sci Technol, 44, 763-771 https://doi.org/10.9721/KJFST.2012.44.6.763
  36. Lim JK, Chung GY, Jeong HJ (2001) Evaluation of the antioxidant potential and identification of active principles of Solanum nigrum L. on antioxidant defense systems. Korean J Life Sci, 11, 509-516
  37. Jeong KS, Lee NG (2009) Functional properties and antioxidant effects of Solanum nigrum-ethanol extract. J Environl Sci, 18, 1207-1214
  38. Jo JJ, Shin MG, Kim ES, Lee YS, Shin YJ, Jeon SY (2014) Cytoprotective effects of Platycodon grandiflorus (Jacq.) A.DC on C6 glioma cell apoptosis by oxidative stress. Korean J Oriental Physiology Pathology, 28, 396-402
  39. Kim SY, Park E, Park JA, Choi BS, Kim S, Jeong G, Kim CS, Kim DK, Kim SJ, Chun HS (2010) The plant phenolic diterpene carnosol suppresses sodium nitroprusside-induced toxicity in C6 glial cells. J Agric Food Chem, 58, 1543-1550 https://doi.org/10.1021/jf903294x
  40. Tsai YD, Hsu HF, Chen ZH, Wang YT, Huang SH, Chen HJ, Wang CP, Wang SW, Chang CC, Houng JY (2014) Antioxidant, anti-inflammatory, and anti-proliferative activities of extracts from different parts of farmed and wild Glossogyne tenuifolia. Ind Crop Prod, 57, 98-105 https://doi.org/10.1016/j.indcrop.2014.03.033
  41. Pacifico S, Piccolella S, Galasso S, Fiorentino A, Kretschmer N, Pan SP, Bauer R, Monaco P (2016) Influence of harvest season on chemical composition and bioactivity of wild rue plant hydroalcoholic extracts. Food Chem Toxicol, 90, 102-111 https://doi.org/10.1016/j.fct.2016.02.009
  42. Oh JS (2012) Seed germination and plant growth characteristics of Solanum nigrum Linne influenced by seed soaking and chilling treatments. MS Thesis, Sunchon National University, Korea, P 17-20
  43. Green LM, Reade JL, Ware CF (1984) Rapid colorimetric assay for cell viability: application to the quantitation of cytotoxic and growth inhibitory lymphokines. J Immunol Methods, 70, 257-268 https://doi.org/10.1016/0022-1759(84)90190-X
  44. Jwa CS, Yang YT, Koh JS (2000) Changes in free sugars, organic acids, free amino acids and minerals by harvest time and parts of Acanthopanax koreanum. J Korean Soc Agric Chem Biotechnol, 43, 106-109
  45. Jing H, Kitts D (2004) Antioxidant activity of sugarlysine Maillard reaction products in cell free and cell culture systems. Arch Biochem Biophys, 429, 154-163 https://doi.org/10.1016/j.abb.2004.06.019