DOI QR코드

DOI QR Code

Anti-inflammatory Effect of Coptidis Rhizoma Extract

황련(黃連) 추출물의 항염효능에 관한 연구

  • Lee, Jeon-Woo (Department of Herbology, College of Oriental Medicine, Gachon University) ;
  • Han, Hyo-Sang (Department of Health Administration, College of Social Sciences, Joongbu University) ;
  • Lee, Young-Jong (Department of Herbology, College of Oriental Medicine, Gachon University)
  • 이전우 (가천대학교 한의과대학 본초학교실) ;
  • 한효상 (중부대학교 보건행정학과) ;
  • 이영종 (가천대학교 한의과대학 본초학교실)
  • Received : 2014.08.18
  • Accepted : 2014.09.15
  • Published : 2014.09.30

Abstract

Objectives : This research has been done to investigate the anti-inflammatory effect of Coptidis Rhizoma extracts. Method : Coptidis Rhizoma was extracted by $100^{\circ}C$ water. The extract (CC : Extract of Coptis chinensis rhizome) was used to examine its effects on the cell viability of mouse macrophage Raw 264.7 cell line. Also the production of nitric oxide (NO), the c-jun N-terminalkinase (JNK) activation and the production of cytokines such as (IL)-5 were evaluated in lipopolysaccharide (LPS)-stimulated Raw 264.7 cells. After the CC and LPS were applied to Raw 264.7 cells which were cultured for 24 hours, the MTT assay was performed. Result : The CC extracts didn't affect the viability of macrophage cells. However, the extracts inhibited the NO production and the JNK activation significantly in LPS-stimulated macrophage cells treated with 100 and $200{\mu}g/mL$ concentrations. The CC extract, also, impeded the production of inflammation-related factors and cytokines such as KC, VEGF, MCP-1, GM-CSF, IL-$1{\alpha}$, IL-5, IL-6, and IL-12p40 in LPS-stimulated macrophage cells at the concentration higher than $25{\mu}g/mL$. The production of basic-FGF concentration of 50 and $100{\mu}g/mL$, the production of IP-10 at $100{\mu}g/mL$, and the production of IFN-${\gamma}$ at $25{\mu}g/mL$, respectively. Conclusion : The CC prepared using $100^{\circ}C$ water showed the significant anti-inflammatory effect such as the inhibition not only on the production of NO, KC, VEGF, MCP-1, GM-CSF, IL-$1{\alpha}$, IL-5, IL-6, and IL-12p40 in LPS-stimulated macrophage cells at or higher than the concentration of $25{\mu}g/mL$, but also on the JNK activation at 100 and $200{\mu}g/mL$.

Keywords

References

  1. Wu B. Shennongbencaojing. Beijing : Kexuejishuwenxian publisher. 1996 : 24.
  2. Jiangsuxinyixueyuan. Zhongyaodacidian. Shanghai : Shanghaikexuejishuchubanshe. 1977 : 2022-30.
  3. Li SZ. Bencaogangmu. Seoul : Komoonsa. 1975 : 447-52.
  4. Korea Food and Drug Administration. The Korean Pharmacopoeia Tenth Edition. Seoul : Korea Food and Drug Administration. 2007 : 995-6.
  5. State Administration of Traditional chiense medicine of the People's Republic of China. Zhonghuabencao. Vol. 4. Shanghai : Shanghai Scientific and Technical Publishers. 1999 : 213-23.
  6. Xiao PG. Xinbianzhongyaozhi. Vol 3. Beijing : Huaxuegongye publisher. 2002 : 894-901.
  7. Doh ES. Antifungal Activity or Coptis japonica Root-stem Extract and Identification of Antifungal Substances. Korean J Plant Resources. 1999 ; 12(4) : 260-8.
  8. Huang WM, Yan H, Jin JM, Yu C, Zhang H. Beneficial effects of berberine on hemodynamics during acute ischemic left ventricular failure in dogs. Beneficial effects of berberine on hemodynamics during acute ischemic left ventricular failure in dogs. Chin Med J (Engl). 1992 ; 105(12) : 1014-9.
  9. Yoon SH, Ha H, Seo MJ. Effect of Coptis Rhizoma on Benzo (a) pyrene-Induced Hepatotoxicity. Kor J Environ Toxicol. 1993 ; 8(1-2) : 31-5.
  10. Lee DU, Chang KC. Bronchodilatory Effects of Coptidis Rhizomas in Isolated Rat Trachea. J Pharm Soc Korea. 1997 ; 41(6) : 797-801.
  11. Yamamoto K, Takase H, Abe K, Saito Y, Suzuki A. Pharmacological studies on antidiarrheal effects of a preparation containing Berberine and Geranii Herba. Nihon Yakurigaku Zasshi. 1993 ; 101(3) : 169-75. https://doi.org/10.1254/fpj.101.3_169
  12. Jung HW, Park YK. Effects of subfractions of Coptidis Rhizoma extract on the nitric oxide production in LPS-stimulated BV2 microglial cells. Kor J Herbology. 2007 ; 22(2) : 73-8.
  13. Kim JH, Lee SJ, Han YB, Kim JB. Identification of Active Component Isolated from Croton tiglium and Coptis Japonica Aqueous Mixture ( CP2 ) and Studies of Its Cytotoxic Effect. J Pharm Soc Korea. 1994 ; 38(1) : 31-7.
  14. Song KB, Kong YH, You HK, Shin HS. Effects of Rhizoma Coptidis on Cellular Activity and IL-6 Production of LPS-treated Periodontal Ligament Cells. J Periodontal Implant Sci. 1996 ; 26(3) : 641-54.
  15. Yoon KR, Kim YJ, Lee E, Lee JM. Anti-inflammatory Effect of Coptidis Rhizoma. Kor J Herbology. 2009 ; 24(3) : 79-86.
  16. Kim JM, Jung HA, Choi JS, Lee NG. Identification of anti-inflammatory target genes of Rhizoma coptidis extract in lipopolysaccharide-stimulated RAW264.7 murine macrophage-like cells. J Ethnopharmacol. 2010 ; 130(2) : 354-62. https://doi.org/10.1016/j.jep.2010.05.022
  17. Ferrari M, Fornasiero MC, Isetta AM. MTT colorimetric assay for testing macrophage cytotoxic activity in vitro. J Immunol Methods. 1990 ; 131(2) : 165-72. https://doi.org/10.1016/0022-1759(90)90187-Z
  18. Weissman BA, Gross SS. Measurement of NO and NO synthase. Curr Protoc Neurosci. 2001 ; 7 : 13.
  19. Johnson FM, Saigal B, Tran H, Donato NJ. Abrogation of signal transducer and activator of transcription 3 reactivation after Src kinase inhibition results in synergistic antitumor effects. Clin Cancer Res. 2007 ; 13(14) : 4233-44. https://doi.org/10.1158/1078-0432.CCR-06-2981
  20. Lee KS, Chung JH, Lee KH, Shin MJ, Oh BH, Hong CH. Bioplex analysis of plasma cytokines in Alzheimer's disease and mild cognitive impairment. Immunol Lett. 2008 ; 121(2) : 105-9. https://doi.org/10.1016/j.imlet.2008.09.004
  21. Schmeller T, Latz-Bruning B, Wink M. Biochemical activities of berberine, palmatine and sanguinarine mediating chemical defence against microorganisms and herbivores. Phytochemistry. 1997 ; 44(2) : 257-66. https://doi.org/10.1016/S0031-9422(96)00545-6
  22. Bost F, McKay R, Bost M, Potapova O, Dean NM, Mercola D. The Jun kinase 2 isoform is preferentially required for epidermal growth factor-induced transformation of human A549 lung carcinoma cells. Mol Cell Biol. 1999 ; 19(3) : 1938-49. https://doi.org/10.1128/MCB.19.3.1938
  23. Sayama K, Hanakawa Y, Shirakata Y, Yamasaki K, Sawada Y, Sun L, Yamanishi K, Ichijo H, Hashimoto K. Apoptosis signal-regulating kinase 1 (ASK1) is an intracellular inducer of keratinocyte differentiation. J biol chem. 2001 ; 276(2) : 999-1004. https://doi.org/10.1074/jbc.M003425200
  24. Zeng X, Moore TA, Newstead MW, Deng JC, Lukacs NW, Standiford TJ. IP-10 mediates selective mononuclear cell accumulation and activation in response to intrapulmonary transgenic expression and during adenovirus-induced pulmonary inflammation. J Interferon Cytokine Res. 2005 ; 25(2) : 103-12. https://doi.org/10.1089/jir.2005.25.103
  25. Conti P, Pang X, Boucher W. Monocyte chemotactic protein-1 is a proinflammatory chemokine in rat skin injection sites and chemoattracts basophilic granular cells. Int Immunol. 1997 ; 9(10) : 1563-70. https://doi.org/10.1093/intimm/9.10.1563
  26. Van Bruggen N, Thibodeaux H, Palmer JT, Lee WP, Fu L, Cairns B, Tumas D, Gerlai R, Williams SP, van Lookeren CM, Ferrara N. VEGF antagonism reduces edema formation and tissue damage after ischemia/reperfusion injury in the mouse brain. J Clin Invest. 1999 ; 104(11) : 1613-20. https://doi.org/10.1172/JCI8218
  27. Bidzhekov K, Zernecke A, Weber C. MCP-1 induces a novel transcription factor with proapoptotic activity. Circ Res. 2006 ; 98(9) : 1107-9. https://doi.org/10.1161/01.RES.0000223483.12225.80
  28. Geijsen N, Koenderman L, Coffer PJ. Specificity in cytokine signal transduction: lessons learned from the IL-3/IL-5/GM-CSF receptor family. Cytokine Growth Factor Rev. 2001 ; 12(1) : 19-25. https://doi.org/10.1016/S1359-6101(00)00019-8
  29. Doyle SE, Gasson JC. Characterization of the role of the human granulocyte-macrophage colony-stimulating factor receptor alpha subunit in the activation of JAK2 and STAT5. Blood. 1998 ; 92(3) : 867-76.
  30. Phun KH. Molecular Immunological Aspects of Cytokines (Interleukins). Korean J Nephrol. 1992 ; 11(6) : 19-32.
  31. Nazarenko I, Marhaba R, Reich E, Voronov E, Vitacolonna M, Hildebrand D, Elter E, Rajasagi M, Apte RN, Zoller M. Tumorigenicity of IL-1alpha-and IL-1beta-deficient fibrosarcoma cells. Neoplasia. 2008 ; 10(6) : 549-62. https://doi.org/10.1593/neo.08286
  32. Lampinen M, Carlson M, Sangfelt P. IL-5 and TNF-&agr; Participate in Recruitment of Eosinophils to Intestinal Mucosa in Ulcerative Colitis. Dig Dis Sci. 2001 ; 46(9) : 2004-9. https://doi.org/10.1023/A:1010659803912
  33. Kishimoto T, Akira S, Taga T. Interleukin-6 and its receptor: a paradigm for cytokines. Science. 1992 ; 258(5082) : 593-7. https://doi.org/10.1126/science.1411569