Effect of Water Extract of Peonia Suffruticosa and Prunus Percica on Anti-inflammation

목단피((牧丹皮).도인(桃仁) 배합(配合)이 항염증(抗炎症) 작용(作用)에 미치는 영향

  • Kim, Young-Il (Noockdang Oriental Clinic) ;
  • Lee, Sung-Jun (Dept. of Oriental Medical Prescription, Wonkwang University) ;
  • Huh, Jin (Dept. of Oriental Medical Prescription, Wonkwang University) ;
  • Lee, Tae-Hyung (Dept. of Oriental Medical Prescription, Wonkwang University) ;
  • Shin, Dong-Gean (Dept. of Oriental Medical Prescription, Wonkwang University) ;
  • Lee, Jae-Cheol (Dept. of Oriental Medical Prescription, Wonkwang University) ;
  • Shin, Yong-Seo (H&BT Co.,Ltd R/D Center) ;
  • Yun, Young-Gab (Dept. of Oriental Medical Prescription, Wonkwang University)
  • 김영일 (노옥당한의원) ;
  • 이성준 (원광대학교 한의과대학 방제학교실) ;
  • 허진 (원광대학교 한의과대학 방제학교실) ;
  • 이태형 (원광대학교 한의과대학 방제학교실) ;
  • 신동근 (원광대학교 한의과대학 방제학교실) ;
  • 이재철 (원광대학교 한의과대학 방제학교실) ;
  • 신용서 ((주)에이치앤비티 R/D센터) ;
  • 윤용갑 (원광대학교 한의과대학 방제학교실)
  • Received : 2010.05.19
  • Accepted : 2010.06.12
  • Published : 2010.06.30

Abstract

Paeonia Suffruticosa and Prunus Persica have been used as oriental medicine for removal of fever, alleviation of pain, an anti-phlogistic effect and removal of extravasated blood. However, it has been never shown the effects of these herbal medicines on anti-inflammatory processes. This experiment was performed to show how these herbs could act as anti-inflammatory medicines at cellular level. Anti-inflammation effects of water extracts from Paeonia Suffruticosa and Prunus Persica as well as their mixture have been investigated, and the results were follows; 1) each extract slightly suppressed the expression and production of inflammatory mediators and enzymes such as NO, iNOS, IL-$1{\beta}$, and TNF-$\alpha$ in lipopolysaccharid(LPS)-stimulated RAW264.7 cells and mouse primary peritoneal macrophages in a dose-dependent manner. These suppressive effects, however, were synergistically increased by their mixture. 2) Each extract of Paeonia Suffruticosa and Prunus Persica insignificantly suppressed the activation and activity of NF-${\kappa}B$ in LPS-stimulated RAW264.7 cells, which controls the expression of inflammatory mediators such as NO, iNOS, IL-$1{\beta}$, and TNF-$\alpha$. However, extract mixture of Paeonia Suffruticosa and Prunus Persica suppressed effectively the activation and activity of NF-${\kappa}B$. 3) Each of Paeonia Suffruticosa and Prunus Persica induced translocation of NF-${\kappa}B$ to the nucleus from the cytosol and DNA-binding activity of nuclear NF-${\kappa}B$ in LPS-activated RAW264.7 cells. The extract mixture of Paeonia Suffruticosa and Prunus Persica showed more significant suppression of the NF-${\kappa}B$ translocation and its DNA-binding activity, as compared to those of the each extract. These results suggest that the extract mixture of Paeonia Suffruticosa and Prunus Persica may affect different control mechanisms for NF-${\kappa}B$ activation and the expression and production of NF-${\kappa}B$-dependent inflammatory mediators, indicating that this extract mixture may be useful for treatment of inflammatory diseases.

Keywords

References

  1. 許 浚. 東醫寶鑑. 서울:법인문화사. 1999:2994, 2683, 383-96, 378-9.
  2. 申佶求. 申氏本草學. 서울:壽文社. 1982:562, 728.
  3. 辛民敎. 臨床本草學. 서울:永林社. 1997:385-6, 540-2.
  4. 鄭虎占. 中藥現代硏究與應用. 北京:學苑出版社. 1988:2369, 3641.
  5. 蔡永敏. 中藥藥理與 臨床應用. 北京:華夏出版社. 1988:321, 70.
  6. 安德均. 韓國本草圖鑑. 서울:敎學社. 1998:97, 542.
  7. 李時珍. 本草綱目. 北京:人民衛生出版社. 1992:1741.
  8. 박영순. 韓方의 藥理解說. 서울:아카데미서적. 2002:86-488, 305-9.
  9. 國家中醫藥管理局. 華本草. 上海:海科學技術出版社. 1998;663-7, 738-42.
  10. 田大準. 實用中藥辭典. 北京:人民衛生出版社. 2002: 943, 1542.
  11. 百科辭典出版社. 實用東醫藥學. 서울:일월서각 1990:168, 281.
  12. 態輔信. 臨床韓藥辭典. 서울:醫聖堂. 1994:131-3, 403-4.
  13. 申載鏞. 方藥合編解說. 서울:成輔社. 1989:591, 584.
  14. 人民衛生. 中藥大辭典. 北京:人民衛生出版社. 1992: 281, 217.
  15. 김동일. 東醫學辭典. 서울:麗江出版社. 1989:329.
  16. 李常仁. 韓藥臨床應用. 서울:成輔社. 1986:108-9.
  17. 이영회. 原色 韓國植物圖鑑. 서울:敎學社. 2002: 344, 204.
  18. 康秉秀. 韓藥臨床配合應用. 서울:永林社. 2004:257, 382.
  19. 鄭有順. 中醫血藥藥理輿應用. 北京:군사의학과학출판사. 1999:180, 294, 326, 327.
  20. 裵元植. 韓方臨床寶鑑. 서울:대성의학사. 2002:548.
  21. 李常仁. 天眞處方解說. 서울:成輔社. 1987:146, 341.
  22. 尹用甲. 東醫方劑와 處方解說. 서울:醫聖堂. 1998:489, 393.
  23. 謝 鳴. 中醫方劑現代硏究. 北京:學苑出版社. 1997:1124, 1600.
  24. 申載鏞. 方藥合編 解說. 서울:成輔社. 1987:320-1.
  25. 藏堃堂. 中醫臨床方劑學. 北京:人民軍醫出版社. 1995:246.
  26. 金相贊. 方劑學. 서울:永林社. 1999:609, 409.
  27. 宗全和. 中醫方劑通釋. 北京:河北科學技術出版社. 1995:券4, 98.
  28. 張錦淸. 實用中醫方劑學. 北京:樂羣出版社. 1876:352, 480.
  29. 虞 搏. 醫學正傳. 서울:成輔社. 1986:309.
  30. 陣 偉. 方劑學. 서울:醫聖堂. 1993:505.
  31. 김갑성. 實用東西醫學 臨床叢書. 서울:정담. 2001:94-95.
  32. 盧永範. 臨床方劑學講座. 서울:대성의학사. 2000:369-70.
  33. 이성춘. 湯證으로보는 東醫寶鑑. 서울:오비기획. 2003:180, 294.
  34. 李 飛. 方劑學. 北京:人民衛生. 2002:299.
  35. 李宇彬. 抗癌 中藥藥理輿 應用. 黑龍江城:黑龍江科學技術出版社. 1999:986, 675.
  36. 任 健. 中國 歷代 名醫名方全集. 北京:學苑出版社. 1996:1025, 1031.
  37. Ueki Y, Miyake S, Tominaga Y, and Eguchi K. Increased nitric oxide levels in patients with rheumatoid arthritis. J Rheumatol. 1996 Feb;23(2):230-6.
  38. Mazzetti I, Grigolo B, Pulsatelli L, Dolzani P, Silvestri T, Roseti L, Meliconi R, and Facchini A. Differential roles of nitric oxide and oxygen radicals in chondrocytes affected by osteoarthritis and rheumatoid arthritis. Clin Sci (Lond). 2001 Dec;101(6):593-9. https://doi.org/10.1042/CS20010030
  39. Moncada S, Palmer RM, and Higgs EA. Biosynthesis of nitric oxide from L-arginine. A pathway for the regulation of cell function and communication. Biochem Pharmacol. 1989 Jun;38(11):1709-15. https://doi.org/10.1016/0006-2952(89)90403-6
  40. Hughes C, Wolos JA, Giannini EH, and Hirsch R. Induction of T helper cell hyporesponsiveness in an experimental model of autoimmunity by using nonmitogenic anti-CD3 monoclonal antibody. J Immunol. 1994 Oct;153(7):3319-25.
  41. Matsuno H, Yudoh K, Katayama R, Nakazawa F, Uzuki M, Sawai T, Yonezawa T, Saeki Y, Panayi G.S, Pitzalis C, and Kimura, T. Rheumatol. The role of TNF-alpha in the pathogenesis of inflammation and joint destruction in rheumatoid arthritis(RA): a study using a human RA/SCID mouse chimera. Rheumatology (Oxford). 2002 Mar;41(3):329-37. https://doi.org/10.1093/rheumatology/41.3.329
  42. Hedbom E. and Hauselmann HJ. Molecular aspects of pathogenesis in osteoarthritis: the role of inflammation. Cell Mol Life Sci. 2002 Jan;59(1):45-53. https://doi.org/10.1007/s00018-002-8404-z
  43. Palmblad K, Erlandsson-Harris H, Tracey KJ, and Andersson U. Dynamics of early synovial cytokine expression in rodent collagen-induced arthritis : a therapeutic study using a macrophage -deactivating compound. Am J Pathol. 2001 Feb;158(2):491-500. https://doi.org/10.1016/S0002-9440(10)63991-0
  44. Strestikova P, Otova B, Filipec M, Masek K, and Farghali H. Different mechanisms in inhibition of rat macrophage nitric oxide synthase expression by FK 506 and cyclosporin A. Immunopharmacol Immunotoxicol. 2001 Feb;23(1):67-74. https://doi.org/10.1081/IPH-100102568
  45. Kang I, Lee WW, and Lee Y. Modulation of collagen-induced arthritis by IL-4 and dexamethasone: the synergistic effect of IL-4 and dexamethasone on the resolution of CIA, Immunopharmacology. 2000 Sep;49(3):317-24. https://doi.org/10.1016/S0162-3109(00)00248-4
  46. Chikanza I. and Fernandes L. Novel strategies for the treatment of osteoarthritis. Expert Opin Investig Drugs. 2000 Sep;1499-510.
  47. Kim YM, de Vera ME, Watkins SC, and Billiar TR. Nitric oxide protects cultured rat hepatocytes from tumor necrosis factor-alpha-induced apoptosis by inducing heat shock protein 70 expression. J Biol Chem. 1997 Jan 10;272(2):1402-11. https://doi.org/10.1074/jbc.272.2.1402
  48. Thornton S, Boivin GP, Kim KN, Finkelman FD, and Hirsch, R. Heterogeneous effects of IL-2 on collagen-induced arthritis. J Immunol. 2000 Aug;165(3):1557-63. https://doi.org/10.4049/jimmunol.165.3.1557
  49. Kim KM, Chun SB, Koo MS, Choi WJ, Kim TW, Kwon YG, Chung HT, Billiar TR, and Kim YM. Differential regulation of NO availability from macrophages and endothelial cells by the garlic component S-allyl cysteine. Free Radical Bio Med. 2001 Jan;30(7):747-56. https://doi.org/10.1016/S0891-5849(01)00460-9
  50. Kiemer AK, Hartung T, Huber C, and vollmar AM. Phyllanthus amarus has anti-inflammatory potential by inhibition of iNOS, COX-2, and cytokines via the NF-${\kappa}B$ pathway. J Hepatol. 2003 Mar;38(3):289-97. https://doi.org/10.1016/S0168-8278(02)00417-8
  51. Xie QW, Kashiwabara Y, and Nathan C. Role of transcription factor NF-${\kappa}B$/Rel in induction of nitric oxide synthase. J Biol Chem. 1994 Feb;269(7):4705-8.
  52. Yokoseki O, Suzuki J, Kitabayashi H, Watanabe N, Wada Y, Aoki M, Morishita R, Kaneda Y, Ogihara T, Futamatsu H, Kobayashi Y, and Isobe M. cis Element decoy against nuclear factor-${\kappa}B$ attenuates development of experimental autoimmune myocarditis in rats. Circ Res. 2001 Nov;89(10):899-906. https://doi.org/10.1161/hh2201.099373
  53. Baeuerle PA, and Baichwal VR. NF-${\kappa}B$ as a frequent target for immunosuppressive and anti -inflammatory molecules. Adv Immunol. 1997; 65:111-37. https://doi.org/10.1016/S0065-2776(08)60742-7
  54. Makarov SS. NF-${\kappa}B$ as a therapeutic target in chronic inflammation: recent advances. Mol Med Today. 2000 Nov;6(11):441-8. https://doi.org/10.1016/S1357-4310(00)01814-1