Anti-Inflammatory Effect of Cornus Walteri

말채나무의 항염증 효과

  • Lee, Sang-Hyun (Department of Pharmaceutical Engineering, College of Health Sciences) ;
  • Yoon, Kwang-Ro (Department of Pharmaceutical Engineering, College of Health Sciences) ;
  • Lee, Eun (Department of Pharmaceutical Engineering, College of Health Sciences) ;
  • Cha, Yun-Yeop (Department of Oriental Rehabilitation Medicine, College of Oriental Medicine, Sangji University)
  • 이상현 (상지대학교 보건과학대학 제약공학과) ;
  • 윤광로 (상지대학교 보건과학대학 제약공학과) ;
  • 이은 (상지대학교 보건과학대학 제약공학과) ;
  • 차윤엽 (한의과대학 한방재활의학과)
  • Received : 2011.08.31
  • Accepted : 2011.11.01
  • Published : 2011.12.25

Abstract

This research seeks a basis for developing new anti-inflammatory medicine by investigating Cornus Walteri extract for its anti-inflammatory effects. After the injection of LPS in to rats with Cornus Walteri extract, its anti-inflammatory effects were compared among the treatment groups. The plasma concentration of IL-$1{\beta}$, IL-6 and TNF-${\alpha}$ peaked at 5h after LPS injection, and the values of the Cornus Walteri extract groups were lower than those of the control group. In the increment of concentration of these cytokines at 2h and 5h after LPS injection, the Cornus Walteri groups were lower than that of control group. The plasma concentration of IL-10 peaked at 5h after LPS injection, and the values of the Cornus Walteri extract groups were higher than those of the control group. In the increment of cytokines concentration at 2h and 5h after LPS injection, the Cornus Walteri groups were higher than that of control group. Liver cytokines measurement was done at 5h after LPS injection. The concentration of liver IL-$1{\beta}$ and IL-6 in the Cornus Walteri groups was lower than that of the control group. The concentrations of liver TNF-${\alpha}$, and IL-10 showed no significant differences among all the treatment groups. In the studies of lipopolysaccharide-exposed Raw 264.7 cells, the concentration of IL-$1{\beta}$, IL-6 and TNF-${\alpha}$ in the lipopolysaccharide-exposed cells groups was higher than that of control group (normal group). However, in lipopolysaccharide-exposed cells groups, they showed lower values than those of control group and these values showed a tendency to decrease in the Cornus Walteri groups. The concentration of IL-10 in the lipopolysaccharide-exposed cells groups was higher than that of control group (normal group), and among the lipopolysaccharide-exposed cells groups, all Cornus Walteri extract groups showed higher values than single lipopolysaccharide-exposed cells groups. This studies have shown that in vitro and in vivo Cornus Walteri extracts are significantly more sensitive to inflammatory cytokines and LPS induced lethality. We conclude that the Cornus Walteri extracts have an functional material for inflammatory activities.

Keywords

References

  1. Chao, C.Y., Yeh, S.L., Lin, M.T., Chen, W.J. Effects of parenteral infusion with fish-oil or safflower-oil emulsion on hepatic lipids, plasma amino acids, and inflammatory mediators in septic rats. Nutrition, 16: 284-288, 2000. https://doi.org/10.1016/S0899-9007(99)00299-3
  2. Abul K., Andrew H Lichtman., Shiv Pillai. Cellular and molecular immunology. 6th edition. p 354, 2007.
  3. Yun, H.J., Heo, S.K., Yi, H.S., Kim, C.H., Kim, B.W., Park, S.D. Anti-inflammatory effect of Injinho-tang in RAW 264.7 Cells. Kor. J. Herbology 23(2):169-178, 2008.
  4. Rabson, A., Roitt, I.M., Delves, P.J. Really essential medical immunology. Blackwell publishing Ltd, Oxford. pp 1-14, 2005.
  5. Boumpas, D.T., Chrousos, G.P., Wilder, R.L., Cupps, T.R., Balow. J.E. Glucocorticoid therapy of immune-mediated diseases: basic and clinical correlates. Ann Intern Med, 119: 1198-1208, 1993. https://doi.org/10.7326/0003-4819-119-12-199312150-00007
  6. Barton, C.C., E.X. Barton, P.E. Ganey, S.L. Kunkel, R.A. Roth. Bacterial lipopolysaccharide enhances aflatoxin B1 hepatotoxicity in rats by a mechanism that depends on tumor necrosis factor-${\alpha}$. Hepatology, 33: 66-73, 2001. https://doi.org/10.1053/jhep.2001.20643
  7. Surh, Y.J. Anti-tumor promoting potential of selected spice ingredients with antioxidative and anti-inflammatory activities: a short review. Food Chem Toxicol 40(8):1091-1097, 2002. https://doi.org/10.1016/S0278-6915(02)00037-6
  8. Seo, W.G., Pae, H.O., Oh, G.S., K.Y. Chai., Kwon, T.O., Yun, Y.G., Kim, N.Y., Chung, H.T. Inhibitory rotundus rhizomes on nitric oxide and superoxide production by murine macrophage cell line, Raw 264.7 cells. J Ethnopharmacol. 76: 59-64, 2001. https://doi.org/10.1016/S0378-8741(01)00221-5
  9. 김태희, 양기숙, 황은진, 박성배. 마황의 면역작용에 미치는 영향. 생약학회지 22(3):183-191, 1991.
  10. Lee E. Anti-inflammatory effect of Scutellariae Radix. Korean J. Plant Res. 20(6): 548-522, 2007.
  11. 남정연, 이현선, 이승웅, 정미연, 최정호, 유은숙, 노문철, 김영국. 감국에서 분리한 Kikkanol F Monoacetate와 5-Hydroxy-6,7,3',4'-tetramethoxy -flavone의 IL-6 생성억제활성. 생약학회지 36(3):186-190, 2005.
  12. 고인자, 유승조, 이은방. 한국산 하고초류의 약물학적 연구(1). 생약학회지 17(3):232-241, 1986.
  13. 김창민, 신민교, 이경순, 안덕균. 중약대사전, 도서출판정담, 서울, p 1718, 1998.
  14. 약품식물학연구회. 신약품식물학. 서울, 학창사, p 336, 1996.
  15. 육창수. 원색한국약용식물도감. 서울, 아카데미서적, p 368, 1993.
  16. 최우회, 박웅양, 황방연, 오갑지, 강신정, 이경순, 노재섭. 말채나무수피의 페놀성 화합물. 생약학회지 29(3):217-224, 1998.
  17. 임채성, 이춘영, 김용무, 이위영, 이해익. 말채나무 추출물의 a-amylase 저해 활성. 한국응용생명화학회지 48(1):103-108, 2005.
  18. Marriot, J.B., Westby, M., Cookson, S., Guckian, M., Goodbourn, S., Muller, G. CC-3052: a water-soluble analog of thalidomide and potent inhibitor of activation-induced TNF-${\alpha}$ production. J Immunol, 161: 4236-4243, 1998.
  19. Mathiak, G., G. Grass., T. Herzmann., T. Luebke., C. Cu-Zetina., S.A. Boehm. Capase-1-inhibitor ac-YVAD-cmk reduces LPS-lethality in rats without affecting haematology or cytokine responses.Br J Pharmacol, 131: 383-386, 2000. https://doi.org/10.1038/sj.bjp.0703629
  20. Eduard, F.M., S.M.R. Martha., P.A. Victor., M. Pablo. Immunomodulatory effects of thalidomide analogs on LPS-induced plasma and hepatic cytokines in the rat. Biochemical pharmacology, 68: 1321-1329, 2004. https://doi.org/10.1016/j.bcp.2004.06.018
  21. Aono, K., K. Isobe., K. Kuichi., Z. Fan., M. Ito, A. Takeuchi. In vitro and in vivo expression of inducible nitric oxide synthase during experimental endotoxemia: involvement of other cytokines. J cell Biochem, 65: 349-358, 1997. https://doi.org/10.1002/(SICI)1097-4644(19970601)65:3<349::AID-JCB5>3.0.CO;2-S
  22. Sang H., G.L. wallis, C.A. Stewart., K. Yashige. Expression of cytokines and activation of transcription factors in lipopolysaccharide-administered rats and their inhibition by phenyl N-tert-butylnitrone (PBN). Arch Biochem Biophys, 363: 341-348, 1999. https://doi.org/10.1006/abbi.1998.1086
  23. Delgado, A.V., McManus, A.T. Chambers JP. production of tumor necrosis factor-alpha, interleukin1-beta, interleukin 2, and interleukin 6, by rat leukocyte subpopulations after exposure to substance P. Neuropeptides. 37(6):355-361, 2003. https://doi.org/10.1016/j.npep.2003.09.005
  24. Hibi, M., Nakajima, K., Hirano, T. IL-6 cytokine family and signal transduction: amodel of the cytokine system. J Mol Med. 4(1):1-12, 1996.
  25. Yoon, H.J., Moon, M.E., Park, H.S., Im, S.Y., Lee, J.H., Kim, Y.H. Researck Papers : Effects of Chitosanoligosaccharide on the C.albicans-induced Inflammatory Effect in Mice and RAW264.7 Macrophage cells. J. Chitin Chitosan. 12(1):15-20, 2007.
  26. Aggarwal, B.B., Kohr, W.J., Hass, P.E., Moffat, B., Spencer, S.A., Henzel, W.J., Bringman, T.S., Nedwin, G.E., Goeddol, D.V., Harkins, R.N. human tumor necrosis factor. Production, purification, and characterization. J Biol Chem. 260(4):2345-2354, 1985.
  27. Bacci, S., Pieri, L., Buccoliero, A.M., Bonelli, A., Taddei, G., romagnoli, P. Smooth muscle cells, dendritic cells and mast cells are sources of TNFalpha and nitric oxide in human carotid artery atherosclerosis. Thromb Res. 122(5):657-667, 2008. https://doi.org/10.1016/j.thromres.2008.04.013
  28. Vilcek, J., Lee, T.H. Tumor necrosis factor. New insights into the molecular mechanisms of its multiple actions. J Biol Chem. 266(12):7313-7316, 1991.
  29. Hamada, E., Nishida, T., Uchiyama, Y., Nakamura, J., Isihara, K., Kazuo, H. Activation of Kupffer cells and caspases-3 involved in rat hepatocyte apoptosis induced by endotoxin. J. Hepatol, 30: 807-818, 1999. https://doi.org/10.1016/S0168-8278(99)80133-0
  30. Pender, S.L., Breese, E.J., Gϋnther, U. Suppression of T-cell-mediated injury in human gut by interleukin 10: Role of matrix metalloproteinases. Gastroenterology. 115: 573-583, 1999.
  31. Clerici, M., Ferrario, E., Trabattoni, D., Viviani, S., Bonfganti, V., Vanzon, D.J. Multiple defects of T helper cell function in newly diagnosed patients with Hodgkin's disease. Eur. J. Cancer. 30A: 1464-1470, 1994.
  32. Kakuma, S., Fukatsu, A., Shinagawa, T., Kurokawa, S., Kusakabe, A. Localization of intra hepatic interleukin-6 in patients with acute and chronic liver disease. J Clin Pathol 45: 408-411, 1992. https://doi.org/10.1136/jcp.45.5.408
  33. Busam, K.J., Bauer, T.M., Bauer, J., Gerok, W., Decker, K. Interleukin-6 release by rat liver macrophages. J Hepatol 11: 367-373, 1990. https://doi.org/10.1016/0168-8278(90)90223-E
  34. Jirik, F.R., Podor, T.J., Hirano, T. Bacterial lipopolysaccharide and inflammatory mediators augment IL-6 secretion by human endothelial cells. J Immunol 142: 144-147, 1989.
  35. Sehgal, P.B., Helfgott, D.C., Santhaanam. Regulation of the acute phase and immune responses in viral disease. Enhanced expression of the beta2-interferon/hepatocyte -stimulating factor/interleukin6 gene in virus-infected human fibroblasts. J Exp Med 167: 1951-1956, 1988. https://doi.org/10.1084/jem.167.6.1951
  36. Frei, K., Malipiero, U.V., Leist, T.P., Zinkernagel, R.M., Sehwab, M.E., Fontana, A. On the cellular source and function of interleukin 6 production in the central nervous system in viral disease. Eur J Immunol 19: 689-694, 1989. https://doi.org/10.1002/eji.1830190418
  37. Beutler, B.B., Greenwald, J.D., Hulmes, M., Chang, Y.C., Pan, J., Maathison. et al. Identity of tumor necrosis factor and the macrophage secreted factor cachectin. Nature, 316: 552-556, 1985. https://doi.org/10.1038/316552a0
  38. Louis, H.O., LeMoine, M.O., Peny, E., Quertinmont, D., Fokan, M., Goldman. et al. Production and role of interleukin-10 in concanavalin A- induced hepatitis in mice. Hepatology, 25: 1382-1389, 1997. https://doi.org/10.1002/hep.510250614
  39. Thompson, K.C., A, Trowern., A, Fowell., M, Marathe., C, Haycock., M.J.P. Arthur et al. Primary rat and mouse hepatic stellate cells express the macrophage inhibitor cytokine interleukin-10 during the course of activation in vitro. Hepatology, 28: 1518-1524, 1998. https://doi.org/10.1002/hep.510280611