Inhibitory Effect of Farfarae Flos Water Extract on COX-2, iNOS Expression and Nitric Oxide Production in lipopolysaccharide - activated RAW 264.7 cells

  • Yoon Tae Gyoung (College of Oriental Medicine, Deagu Hanny University) ;
  • Byun Boo Hyeong (College of Oriental Medicine, Deagu Hanny University) ;
  • Kwon Teag Kyu (College of Medicine, Keimyung University) ;
  • Suh Seong Il (College of Medicine, Keimyung University) ;
  • Byun Sung Hui (College of Oriental Medicine, Deagu Hanny University) ;
  • Kwon Young Kyu (College of Oriental Medicine, Deagu Hanny University) ;
  • Kim Sang Chan (College of Oriental Medicine, Deagu Hanny University)
  • Published : 2004.06.01

Abstract

Farfrae Flos has been clinically used for the treatment of asthma in traditional oriental medicine. There is lack of studies regarding the effects of Farfrae Flos on the immunological activities. The present study was conducted to evaluate the effect of Farfrae Flos on the regulatory mechanism of cytokines and nitric oxide (NO) for the immunological activities in Raw 264.7 cells. In Raw 264.7 cells stimulated with lipopolysaccharide (LPS) to mimic inflammation, Farfrae Flos water extract inhibited nitric oxide production in a dose-dependent manner and abrogated inducible nitric oxide synthase (iNOS) and cyclooxygenase (COX-2). Farfrae Flos water extract did not affect on cell viability. To investigate the mechanism by which Farfrae Flos water extract inhibits iNOS and COX-2 gene expression, we examined the on the phospholylation of inhibitor κBα and production of TNF-α, IL-1β and IL-6. Results provided evidence that Farfrae Flos inhibited the production of interleukin-1β (IL-1β) and the activation of phospholylation of inhibitor κBα in Raw 264.7 cells activated with LPS. These findings suggest that Farfrae Flos can produce anti-inflammatory effect, which may play a role in adjunctive therapy in Gram-negative bacterial infections.

Keywords

References

  1. Evidence-Based Herbal Medicine. Michael R;Irwin Z.
  2. Mutat. Res. v.428 Molecular mechanisms of chemopreventive effects of selected dietary and medicinal Phenolic substances. Y.J. Surh
  3. J. Lab. Clin. Med. v.128 Cyclooxygenase-2 induction: molecular mechnism and pathophysiologyc roles. K.K. Wu
  4. Food Chem Toxicol. v.40 no.8 Anti-tumor promoting potential of selected spice ingredients with antioxidative and anti-inflammatory activities: a short review. Surh YJ.
  5. Mutat Res. Molecular mechanisms underlying chemopreventive activities of anti-inflammatory phytochemicals: down- regulation of COX-2 and iNOS through suppression of NF-kappa B activation. Surh YJ;Chun KS;Cha HH;Han SS;Keum YS;Park KK;Lee SS.
  6. Neuropeptides v.37 no.6 Production of tumor necrosis factor-alpha, interleukin 1-beta, interleukin 2, and interleukin 6 by rat leukocyte subpopulations after exposure to substance P. Delgado AV;McManus AT;Chambers JP.
  7. Surgery v.135 no.5 Interleukin-1 upregulates anaphylatoxin receptors on mononuclear cells. Takabayashi T;Shimizu S;Clark BD;Beinborn M;Burke JF;Gelfand JA.
  8. Adverse effects of Herbal Drugs. v.1 Pyrrolizidine Alkaloids-Tussilago farfara. Westerndorf J.;De Smet PAGM(et al)(Eds.)
  9. Nature v.333 Vascular endothelial cells synthesize nitric oxide from L-arginine. Palmer RM;Ashton DS;Moncada S.
  10. Gut v.47 Inducible nitric oxide synthase; a little bit og good in all of us. Kubes p.
  11. Korean J. Oriental Physiology & Pathology v.16 no.5 Inhibitory effect of Omisodok-eum on the secretion of NO in LPS-stimulated mouse peritoneal macrophages. H.J. Park;S.W. Yoon;J.W. Yoon;H.J. Yoon;W.S. Ko.
  12. AJP New insight into the role of nuclear factor- B in cell growth regulation. F Chen;V Castranova;X Shi.
  13. British journal of pharmacology. v.139 Inhibition of lipopolysaccharide-inducible nitric oxide synthase, TNF- and COX-2 expression by sauchinone effects on I- B phosphorylation, C/EBP and AP-1 activation. Lee AK;Sung SH;Kim YC;Kim SG.
  14. Ann Intern Med v.119 Plasma cytokine and endotoxin levels correlate with survival in patients with the sepsis syndrome. Casey LC;Balk RA;Bone RC.
  15. Eur J Clin Invest. v.23 Pancreatic beta-cell function and interleukin-1b in plasma during the acute phase response in patients with major burn injuries. Wogensen L;Jensen M;Svensson P;Worsaae H;Welinder B;Nerup J.
  16. Transplantation v.63 Interleukin 1 receptor blockade reduces tumor necrosis factor production, tissue injury, and mortality after hepatic ischemia-reperfusion in the rat. Shito M;Wakabayashi G;Ueda M;Shimazu M;Shirasugi N;Endo M(et al.)
  17. J Thorac Cardiovasc Surg v.98 Induction of interleukin-1 production in patients undergoing cardiopulmonary bypass. Haeffner-Cavaillon N;Roussellier N;Ponzio O;Carreno M-P;Laude M;Carpentier A(et al.)