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Effect of Cheongpyesagan-tang on LPS Induced Inflammation in RAW 264.7 Cells

LPS로 유도된 RAW 264.7 cell의 염증반응에서 청폐사간탕(淸肺瀉肝湯)의 항염증 효과

  • 김태연 (세명대학교 한의과대학) ;
  • 임강현 (세명대학교 한의과대학)
  • Received : 2019.01.03
  • Accepted : 2019.02.20
  • Published : 2019.02.25

Abstract

Cheongpyesagan-tang (CP) is one of the traditional medicinal prescription to treat Taeumin (太陰人)'s disease. It has been commonly used for the treatment of stroke, arthritis, diabetes and obesity. In this study, we investigated an anti-inflammatory potential of CP water extract. We examined the effects of CP on the lipopolysarccharide (LPS)-induced production of nitric oxide (NO) and prostaglandin $E_2$ ($PGE_2$). We also examined the levels of protein or mRNA of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2) and proinflammatory cytokines in RAW 264.7 cells. CP inhibited NO and $PGE_2$ production in a dose dependent manner and decreased the protein and mRNA expression of iNOS and COX-2. Also, CP decreased the mRNA expression of interleukin-6 (IL-6), interleukin-$1{\beta}$ (IL-$1{\beta}$), tumor necrosis factor-${\alpha}$ (TNF-${\alpha}$). These results suggest that CP has potential as anti-inflammatory therapeutic medicine.

Keywords

References

  1. Kindt TJ, Goldsby RA, Osborne BA. Innate immunity : Tenney S. Kuby Immunology. 6th ed. New York:Freeman press;2007. p. 52-73.
  2. Jou IL. Chronic Inflammatory Disease Research Center. Seoul:Ajou University;2012. 122 p.
  3. Yun HJ, Hoe SK. Anti-inflammatory Effect of Injinho-tang in RAW 264.7 cells. Kor J Herbol. 2008;23(2):169-78.
  4. Textbook Compilation Committee of Pathology in Korean Medicine. Pathology in Korean Medicine. 3rd ed. Yongin:Hanuimunhwasa;2017. p. 54-7, 60, 70.
  5. National College of Korean Medicine Collaborative Textbook Compilation Committee. Herbology. Seoul:Younglim Publishing Inc;2000. p. 127, 131, 518, 534, 540, 583.
  6. Lee JM. Dongeuisusebowon. Seoul:Henglim Publishing Inc;1986. p. 7-13, 115, 137-8.
  7. Hwang JH, Jang ES, Yoo JH, Lee SW. Clinical study on the utilization of Yeoldahanso-tang and Cheongpyesagan-tang. Korean Inst Orient Med. 2008;14(2): 101-6.
  8. Choi DJ, Jung WS, Moon SK, Cho KH, Kim YS, Bae HS. The clinical efficacy of Chungpyesagan-tang on acute stroke. J Korean Orient Med. 2002;23(4):9-14.
  9. Jeong CG, Kim EY, Shin JW, Sohn YJ, Lee HS, Jung HS, et al. Effect of Chungpaesagan-tang on ischemic damage induced by middle cerebralartery occlusion in diabetic rats. J Korean Orient Med. 2005;26(2):217-30.
  10. Kim JY, Shin MR, Heo WY, Kim DR, Weon JJ. The effects of Chungpyesagan-tang on the recovery of liver function in rat injured by CCl4. J Sasang Const Med. 2005;17(1):130-41.
  11. Ahn HM, Han SY, Kim JH, Rho TW, Chong MS, Kim YK. Effects of Cheongpyesagan-tang and YKK012 on in vitro and in vivo colon cancer cell growth with and without CPT-11. Kor J Herbol. 2015;30(1):33-43. https://doi.org/10.6116/KJH.2015.30.1.33.
  12. Park YJ, Kim SJ, Yang GE, Lee MJ, Lee JS, Kang DH, et al. Anti-platelet aggregation effect of Cheongpyesagan-tang in vitro. Korean J Orient Int Med. 2010; 31(4):714-21.
  13. Hong SG, Joo KB, Jin KY, Mo KS, Wuk CD. Protective effects of Chungpesagan-tang against ischemia/reperfusion induced cell injury. Korea Inst Orient Med. 2000;54(1):111-7.
  14. Kim DL, Song YB. An experimental study of the effect by Chongshimyonjatang and Chongpyesagantang on immune response and anti-allergic reaction to rats and mice. J KyungHee Orient Med Coll. 1991;14:131-60.
  15. Kim JH, Park SS. The Effect of Chungpyesagantang on Lipopolysaccharide induced Arthritis in Mice. J Sasang Const Med. 2002;14(3):114-31.
  16. Koo JS. Effects of Chungpyesagantang on the diabetic rats induced by streptozotocin. J Korean Orient Pediatr. 1997;11(1):227-48.
  17. Song MY, Kim SS, Shin HD. The clinical study about the effect of Chugpaesagan-tang and Taeumjoui-tang on Taeumin obesity after fasting therapy. J Orient Rehab Med. 1998;8(1):34-56.
  18. Kim EY, Sul YK, Choi JJ, Jeon SH, Kim H, Kim JW. Effect of Cheongpesagan-tang on the change of inhibitory effect against lipase activity and weight loss, plasma and UCP1, 2mRNA expression in db/db mouse. J Sasang Const Med. 2007;19(1):171-85.
  19. Bae JH, Lee JS, Chung SH, Kim SS, Shin HD. Effect of Cheongpesagan-tang on the changes of the weight, plasma and UCP mRNA expression in obese SD rats induced high fat feed. J Orient Rehabil Med. 2002;12(1):133-56.
  20. Huh SY, Kang HS. Experimental study on the effect of Chungpesagantang in obese rats. J Orient Rehabil Med. 1998;8(2):106-18.
  21. Kim BH, Lee YT, Kang KH. Codonopsis Lanceolata Inhibits Inflammation through Regulation of MAPK in LPS-stimulated RAW264.7 cells. J Physiol Pathol Korean Med. 2010;24(1):80-4.
  22. Dawson TM, Dawson VL, Snyder SH. A novel neuronal messenger molecule in brain:The free radical, nitric oxide. Ann Neurol. 1992;32:297-311. https://doi.org/10.1002/ana.410320302
  23. Wang MJ, Lin WW, Chen HL, Chang YH, Ou HC, Kuo JS, et al. Silymarin protects dopaminergic neurons against lipopolysaccharide-induced neurotoxicity by inhibiting microglia activation. Eur J Neurosci. 2002;16(11):2103-12. https://doi.org/10.1046/j.1460-9568.2002.02290.x
  24. Hanisch UK. Microglia as a source and target of cytokines. Glia. 2002;40(2):140-55. https://doi.org/10.1002/glia.10161
  25. Chen W, Tang Q, Gonzales MS, Bowden GT. Role of p38 MAP kinases and ERK in mediating ultraviolet-B induced cyclooxygenase-2 gene expression in human keratinocytes. Oncogene. 2001;20(29):3921-6. https://doi.org/10.1038/sj.onc.1204530
  26. Marina L, Kamal RM, Andrew F, Gary B, Jeremy S, Andrew RC. Regulation of Cyclooxygenase 2 mRNA Stability by the Mitogen-Activated Protein Kinase p38 Signaling Cascade. Mol Cell Biol. 2000;20(12):4265-74. https://doi.org/10.1128/MCB.20.12.4265-4274.2000
  27. Mitchell JA, Larkin S, Williams TJ. Cyclooxygenase-2: regulation and relevance in inflammation. Biochemical Pharmacology. 1995;50(10):1535-42. https://doi.org/10.1016/0006-2952(95)00212-X
  28. Crofford LJ, Lipsky PE, Brooks P, Abramson SB, Simon LS, Van de Putte LB. Basic biology and clinical application of specific cyclooxygenase-2 inhibitors. Arthritis Rheum. 2000;43(1):4-13. https://doi.org/10.1002/1529-0131(200001)43:1<4::AID-ANR2>3.0.CO;2-V
  29. Raabe T, Bukrinsky M, Currie RA. Relative contribution of transcription and translation to the induction of tumor necrosis factor-alpha by lipopolysaccharide. J Biol Chem. 1998;273(2):974-80. https://doi.org/10.1074/jbc.273.2.974
  30. Lee BJ, Heo H, Oh SC, Lew JH. Comparison study of Korean and Chinese ginsengs on the regulation of Lymphocyte proliferation and cytokine production. J Ginseng Res. 2008;32(3):250-6. https://doi.org/10.5142/JGR.2008.32.3.250
  31. 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 macrophage. Biol Pharm Bull. 2004;27(5):617-20. https://doi.org/10.1248/bpb.27.617
  32. Lazarov S, Balutsov M, lanev E. The role of bacterial endotoxins, receptors and cytokines in the pathogenisis of septic(endotoxin) shock. Vutr Boles. 2000;32(4):33-40.
  33. Berek JS, Chung C, Watson JM, Knox RM, Martinez-Maza O. Serum interleukin-6 levels correlate with disease status in patients with epithelial ovarian cancer. Am J Obstet Gynecol. 1991;164(4):1038-42. https://doi.org/10.1016/0002-9378(91)90582-C
  34. Dupont N, Jiang S, Pilli M, Ornatowski W, Bhattacharya D, Deretic V. Autophagy-based unconventional secretory pathway for extracellular delivery of IL-$1{\beta}$. EMBO J. 2011;30:4701-11. https://doi.org/10.1038/emboj.2011.398
  35. Narayanan P, Sonika P. Tumor Necrosis Factor-${\alpha}$ Signaling in Macrophages. Crit Rev Eukaryot Gene Expr. 2010;20(2):87-103. https://doi.org/10.1615/CritRevEukarGeneExpr.v20.i2.10

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