DOI QR코드

DOI QR Code

Effect of Hibisci Flos on Inflammatory Cytokines Production in lipopolysaccaride-stimulated Raw 264.7 Macrophages

목근화(木槿花) 물추출물의 항염효능에 관한 연구

  • Lee, Dong-Min (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)
  • 이동민 (가천대학교 한의과대학 본초학교실) ;
  • 한효상 (중부대학교 보건행정학과) ;
  • 이영종 (가천대학교 한의과대학 본초학교실)
  • Received : 2013.08.15
  • Accepted : 2013.09.17
  • Published : 2013.09.30

Abstract

Objectives : Hibisci Flos has long been used for inflammatory diseases in traditional Korean medicine. However, little scientific investigation has been carried out. The aim of the present study is to investigate the effect of Hibisci Flos water extract (HF) on inflammatory cytokines production in Raw 264.7 cells stimulated by lipopolysaccaride (LPS). Method : HF was prepared by extracting with boiling water for 2 hours. We observed the cell viability of mouse macrophage Raw 264.7, the production of nitric oxide (NO) and the inflammatory cytokines such as interleukin (IL)-4, IL-5, IL-10, IL-15, tumor necrosis factor-${\alpha}$ (TNF-${\alpha}$), interferon-gamma (IFN-${\gamma}$), vascular endothelial growth factor (VEGF), granulocyte macrophage-colony stimulating factor (GM-CSF), and macrophage colony-stimulating factor (M-CSF) in Raw 264.7 cells stimulated by LPS. Result : The MTT assay was carried out to check the cellular toxicity of HF. No significant toxicity was observed in the experiment. HF significantly inhibited the increase of NO in the macrophages induced by LPS after 24 hour treatment. HF significantly inhibited the production of IL-4, IL-5, IL-10, IL-15, TNF-${\alpha}$, IFN-${\gamma}$, VEGF, GM-CSF and M-CSF in the Raw 264.7 cells induced by LPS in the concentration of $25{\mu}g/mL$ or higher. Conclusion : These results suggest that HF might have regulatory effects on LPS-induced inflammatory cytokine production, which might explain its beneficial effect in the treatment of inflammatory disease.

Keywords

References

  1. State Administration of Traditional chiense medicine of the People's Republic of China. Zhonghuabencao. Vol. 9. Shanghai : Shanghai Scientific and Technical Publishers. 1999 : 354-6.
  2. Wu Y. Rihuazibencao. Hefei : AnhuiKexuejishu publisher. 2005 : 148-9.
  3. Choi GY, Yoon TS, Choo BK, Lee AY, Chae SU, Ju YS, Kim HK. Study on the Medicinal Parts and Expected Efficacys of the Hibiscus syriacus by Literature Review on the Classics of Oriental Medicine. Kor J Orient Med. 2007 ; 13(2) : 27-36.
  4. Tian DH. Shiyongzhongyaocidian. Beijing : Renminweisheng publisher. 2002 : 291-2.
  5. Yun BS, Lee IK, Ryoo IJ, Yoo ID. Coumarins with monoamine oxidase inhibitory activity and antioxidative coumarins-lignans from Hibiscus syriacus. J Nat Prod. 2001 ; 64(9) : 1238-40. https://doi.org/10.1021/np0100946
  6. Kwon SW, Hong SS, Kim JI, Ahn IH. Antioxidant properties of heat-treated Hibiscus syriacus. Izv Akad Nauk Ser Biol. 2003 ; (1) : 20-1.
  7. Choi KW, Lee SR, Jung IC. Effects of ChongMyung-Tang and ChongMyung-Tang added Hibiscus syriacus Hot water extract & Ultra-fine Powder on Microglia and Memory Deficit Model. Kor J Orient Physiol Pathol. 2006 ; 20(5) : 1200-10.
  8. Park JU, Jung IC, Lee SR. The Effects of ChongMyungTang(CMT) and ChongMyungTang added Hibiscus syriacus(MCMT) Extract on the Alzheimer's Disease Model Induced by CT-105 and $\beta$ A. J Orient Neuropsychiatry. 2006 ; 17(1) : 37-57.
  9. Park GG. Gugangsaenghwahak. Seoul : Gunja publisher. 1999 : 318-25.
  10. Weissman BA, Gross SS. Measurement of NO and NO synthase. Curr Protoc Neurosci. 2001 ; 7(7) : 13.
  11. Politch JA, Tucker L, Bowman FP, Anderson DJ. Concentrations and significance of cytokines and other immunologic factors in semen of healthy fertile men. Hum Reprod. 2007 ; 22(11) : 2928-35. https://doi.org/10.1093/humrep/dem281
  12. Gangsosinuihakwon. Jungyakdasajeon Vol. 4. Seoul : Jeongdam publisher. 1998 : 1766-7.
  13. Lee CB. Wonsaekdaehansikmuldogam. Seoul : Hyangmunsa. 2006 : 736.
  14. Lu GP, Liu LR. Changyongzhongyaocaichuantongjianbie. Beijing : Renminweisheng publisher. 2005 : 465-6.
  15. Yoo KO, Lim HT, Kim JH. Studies on the flavonoids of the Hibiscus syriacus L. complex. Kor J Plant Res. 1996 ; 9(3) : 224-9.
  16. Willoughby DA. Human arthritis applied to animal models. Toward a better therapy. Ann Rheum Dis. 1975 ; 34(6) : 471-8. https://doi.org/10.1136/ard.34.6.471
  17. Lazarov S, Balutsov M, Ianev E. The role of bacterial endotoxins, receptors and cytokines in the pathogenesis of septic (endotoxin) shock. Vutr Boles. 2000 ; 32(4) : 33-40.
  18. Lee ES, Ju HK, Moon TC, Lee E, Jahng Y, Lee SH, Son JK, Baek SH, Chang HW. Inhibition of nitric oxide and tumor necrosis factor-$\alpha$ (TNF-$\alpha$) production by propenone compound through blockade of nuclear factor (NF)-$\kappa{B}$ activation in cultured murine macrophages. Biol Pharm Bull. 2004 ; 27(5) : 617-20. https://doi.org/10.1248/bpb.27.617
  19. Lee TH, Kwak HB, Kim HH, Lee ZH, Chung DK, Baek NI, Kim J. Methanol extracts of Stewartia koreana inhibit cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) gene expression by blocking NF-kappa B transactivation in LPS-activated Raw 264.7 cells. Mol Cells. 2007 ; 23(3) : 398-404.
  20. Nishida T, Yabe Y, Fu HY, Hayashi Y, Asahi K, Eguchi H, Tsuji S, Tsujii M, Hayashi N, Kawano S. Geranylgeranylacetone induces cyclooxygenase-2 expression in cultured rat gastric epithelial cells through NF-$\kappa{B}$. Dig Dis Sci. 2007 ; 52(8) : 1890-6. https://doi.org/10.1007/s10620-006-9661-8
  21. Heo Y, Kim HA. Review on Experimental Methods for Investigation of Atopic Dermatitis. Kor J public health. 2007 ; 44(1) : 81-6.
  22. Bagley CJ, Lopez AF, Vadas MA. Updates on cells and cytokines; New frontiers for IL-5. J Allergy Clin Immunol. 1997 ; 99(6) : 725-8. https://doi.org/10.1016/S0091-6749(97)80002-4
  23. Pajkrt D, Camoglio L, Tiel-van Buul MC, de Bruin K, Cutler DL, Affrime MB, Rikken G, van der Poll T, ten Cate JW, van Deventer SJ. Attenuation of proinflammatory response by recombinant IL-10 in human endotoxemia: effect of timing of recombinant human IL-10 administration. J Immunol. 1997 ; 158(8) : 3971-7.
  24. Giri JG, Ahdieh M, Eisenman J, Shanebeck K, Grabstein K, Kumaki S, Namen A, Park LS, Cosman D, Anderson D. Utilization of the $\beta$ and $\gamma$ chains of the IL-2 receptor by the novel cytokine IL-15. EMBO J. 1994 ; 13(12) : 2822-30.
  25. Carson WE, Ross ME, Baiocchi RA, Marien MJ, Boiani N, Grabstein K, Caligiuri MA. Endogenous production of interleukin 15 by activated human monocytes is critical for optimal production of interferon-$\gamma$ by natural killer cells in vitro. J Clin Invest. 1995 ; 96(6) : 2578-82. https://doi.org/10.1172/JCI118321
  26. Kim YH, Yoon HJ, Moon ME, Lee JH, Park HS, Kim JS. Production of NO, TNF-$\alpha$ and IL-6 by Squalene, Alkoxy Glycerol, Batyl and Chimyl Solutions in RAW 264.7 Macrophage Cells. J Korean Soc Food Sci Nutr. 2005 ; 34(10) : 1503-8. https://doi.org/10.3746/jkfn.2005.34.10.1503
  27. Orme IM, Roberts AD, Griffin JP, Abrams JS. Cytokine secretion by CD4+ T lympocytes aquired in response to mycobacterium tuberculosis infection. J Immunol. 1993 ; 151(1) : 518-25.
  28. Ferrara N, Henzel WJ. Pituitary follicular cells secrete a novel heparin-binding growth factor specific for vascular endothelial cells. Biochem Biophys Res Commun. 1989 ; 161(2) : 851-8. https://doi.org/10.1016/0006-291X(89)92678-8
  29. Dvorak HF, Brown LF, Detmar M, Dvorak AM. Vascular permeability factor/vascular endothelial growth factor, microvascular hyperpemeability, and angiogenesis. Am J Pathol. 1995 ; 146(5) : 1029-39.
  30. Costello RT. Therapeutic use of granulocyte-macrophage colony-stimulating factor (GM-CSF). A review of recent experience. Acta Oncol. 1993 ; 32(4) : 403-8. https://doi.org/10.3109/02841869309093617
  31. Lopez AF, Eglinton JM, Lyons AB, Tapley PM, To LB, Park LS, Clark SC, Vadas MA. Human interleukin-3 inhibits the binding of granulocyte-macrophage colony-stimulating factor and interleukin-5 to basophils and strongly enhances their functional activity. J Cell Physiol. 1990 ; 145(1) : 69-77. https://doi.org/10.1002/jcp.1041450111
  32. Bukowski RM, Budd GT, Gibbons JA, Bauer RJ, Childs A, Antal J, Finke J, Tuason L, Lorenzi V, McLain D. Phase I trial of subcutaneous recombinant macrophage colony-stimulating factor: clinical and immunomodulatory effects. J Clin Oncol. 1994 ; 12(1) : 97-106. https://doi.org/10.1200/JCO.1994.12.1.97
  33. Sakurai T, Suzu S, Yamada M, Yanai N, Kawashima T, Hatake K, Takaku F, Motoyoshi K. Induction of Tumor Necrosis Factor in Mice by Recombinant Human macrophage colony-stimulating Factor. Jpn J Cancer Res. 1994 ; 85(1) : 80-5. https://doi.org/10.1111/j.1349-7006.1994.tb02889.x