References
- Kundu, J.K., Surh, Y.J. Inflammation: gearing the journey to cancer, Mutat Res. 2008;659:15-30. https://doi.org/10.1016/j.mrrev.2008.03.002
- Park CY, Ryu HJ. Inflammation and Obesity. J Korean Soc Endocrinol. 2004; 19:97-108.
- Nathan C. Points of control in inflammation. Nature. 2002;420:846-52. https://doi.org/10.1038/nature01320
- Tracey KJ. The inflammatory reflex. Nature. 2002;420:853-9. https://doi.org/10.1038/nature01321
-
Shin JS, Park YM, Choi JH, Park HJ, Shin MC, Lee YS, et al. Sulfuretin solated from heartwood of Rhus verniciflua inhibits LPS-induced inducible nitric oxide synthase, cyclooxygenase-2, and pro-inflammatory cytokines expression via the down-regulation of
$NF-{\kappa}B$ in RAW 264.7 murine macrophage cells. International Immunopharmacology. 2010;10:943-50. https://doi.org/10.1016/j.intimp.2010.05.007 - Ignarro LJ. Nitric oxide as a unique signaling molecule in the vascular system: a historical overview. J Physiol Pharmacol. 2002;53:503-14.
- Feldmann M, Brennan FM, Chantry D, Haworth C, Turner M, Katsikis P, et al. Cytokine assays: role in evaluation of the pathogenesis of autoimmunity. Immunol Rev. 1991;119:105-23. https://doi.org/10.1111/j.1600-065X.1991.tb00580.x
- Tamir S, Tannenbaum SR. The role of nitric oxide (NO) in the carcinogenic process. Biochimica et Biophysica Acta. 1996;1288:F31-6.
- Rohdewald P. A review of the French maritime pine bark extract (Pycnogenol), a herbal medication with a diverse clinical pharmacology. Int. J. Clin. Pharmacol. Ther. 2002;40:158-68. https://doi.org/10.5414/CPP40158
- Rao YK, Fang SH, Tzeng YM. Inhibitory effects of the flavonoids isolated from Waltheria indica on the production of NO, TNF-a and IL-12 in activated macrophages. Biol. Pharm. Bull. 2005;28:912-5. https://doi.org/10.1248/bpb.28.912
- Lau KM, He ZD, Dong H, Fung KP, But PP. Anti-oxidative, anti-inflammatory and hepato-protective effects of Ligustrum robustum. Journal of Ethnopharmacology. 2002;83:63-71. https://doi.org/10.1016/S0378-8741(02)00192-7
- Lin HM, Yen FL, Ng LT, Lin CC. Protective effects of Ligustrum lucidum fruit extract on acute butylated hydroxytoluene-induced oxidative stress in rats. Journal of Ethnopharmacology. 2007;111:129-36. https://doi.org/10.1016/j.jep.2006.11.004
- Nagy M, Krizkova L, Mucaji P, Kontsekova Z, Sersen F, Krajcovic J. Antimutagenic activity and radical scavenging activity of water infusions and phenolics from Ligustrum plants leaves. Molecules. 2009;14:509-18. https://doi.org/10.3390/molecules14010509
- Sung SH, Kim ES, Lee KY, Lee MK, Kim YC. A new neuroprotective compound of Ligustrum japonicum leaves. Planta edica. 2006;72:62-4. https://doi.org/10.1055/s-2005-873140
- Lee SI, Oh SH, Park KY, Park BH, Kim JS, Kim SD. Antihyperglycemic effects of fruits of privet (Ligustrum obtusifolium) in streptozotocin-induced diabetic rats fed a high fat diet. J Med Food. 2009 Feb;12:109-17. https://doi.org/10.1089/jmf.2007.0000
- Su YW, Chao SH, Lee MH, Ou TY, Tsai YC. Inhibitory effects of citronellol and geraniol on nitric oxide and prostaglandin E production in macrophages. Planta Med. 2010;76:1666-71. https://doi.org/10.1055/s-0030-1249947
- Wang L, Xu ML, Hu JH, Rasmussen SK, Wang MH. Codonopsis lanceolata extract induces G0/G1 arrest and apoptosis in human colon tumor HT-29 cells - Involvement of ROS generation and polyamine depletion. Food and Chem. Toxicol. 2011;49:149-54.
-
Zhang YF, Wang SZ, Li YY, Xiao ZY, Hu ZL, Zhang JP. Sophocarpine and matrine inhibit the production of
$TNF-{\alpha}$ and IL-6 in murine macrophages and prevent cachexia-related symptoms induced by colon 26 adenocarcinoma in mice. Int. Immunopharmacol. 2008;8:1767-72. https://doi.org/10.1016/j.intimp.2008.08.008 - Johansson H, Svartstrom O, Phadnis P, Engman L, Ott MK. Exploring a synthetic organoselenium compound for antioxidant pharmacotherapy-toxicity and effects on ROS-production. Bioorganic & Medicinal Chemistry. 2010;18:1783-8. https://doi.org/10.1016/j.bmc.2010.01.057
- Mercurio F, Zhu H, Murray BW, Shevchenko A, Bennett BL, Li J, et al. IKK-1 and IKK-2: cytokine-activated IkappaB kinases essential for NF-kappaB activation. Science. 1997;278:860-6. https://doi.org/10.1126/science.278.5339.860
- Szabo C. Alterations in nitric oxide production in various forms of circulatory shock. New Horiz. 1995;3:2-32.
- Ahn KB, Aggrawal BB. Transcription factor NF-{kappa} B: a sensor for smoke and stress signals. Ann. NY Acad. Sci. 2005;1056:218-33. https://doi.org/10.1196/annals.1352.026
- Hibi M, Nakajima T, Hirano T. IL-6 cytokine family and signal transduction: a model of the cytokine system. J. Mol. Med. 1996;74:1-12. https://doi.org/10.1007/BF00202068
- Bendtzen K. Interleukin 1, interleukin 6 and tumor necrosis factor in infection, inflammation and immunity. Immunol Lett. 1988;19:183-91. https://doi.org/10.1016/0165-2478(88)90141-1
-
Natarajan K, Manna SK, Chaturvedi MM, Aggarwal BB. Protein Tyrosine Kinase Inhibitors Block Tumor Necrosis Factor-Induced Activation of Nuclear Factor-
${\kappa}B$ , Degradation of$I{\kappa}B{\alpha}$ , Nuclear Translocation of p65, and Subsequent Gene Expression. Archives of Biochemistry and Biophysics. 1992;352:59-70. - Ginn-Pease ME, Whisler RL. Redox signals and NF-B activation in T cells. Free Radical Biology and Medicine. 1998;25:346-61. https://doi.org/10.1016/S0891-5849(98)00067-7
- Forman HJ, Torres M. Redox signaling in macrophages. Molecular Aspects of Medicine. 2001;22:189-216. https://doi.org/10.1016/S0098-2997(01)00010-3
- Lee SH, Soyoola E, Chanmugam P, Hart S, Sun W, Zhong H, et al. Selective expression of mitogen-inducible cyclooxygenase in macrophages stimulated with lipopolysaccharide. J. Biol. Chem. 1992;267:25934-8.
- Yen GC, Duh PD, Huang DW, Hsu CL, Fu TYC. Protective effect of pine (Pinusmorrisonicola Hay.) needle on LDL oxidation and its anti-inflammatory action by modulation of iNOS and COX-2 expression in LPS-stimulated RAW 264.7 macrophages. Food and Chemical Toxicology. 2008;46:175-85. https://doi.org/10.1016/j.fct.2007.07.012
-
Cho W, Nam JW, Kang HJ, Windono T, Seo EK, Lee KT. Zedoarondiol isolated from the rhizoma of Curcuma heyneana is involved in the inhibition of iNOS, COX-2 and pro-inflammatory cytokines via the downregulation of
$NF-{\kappa}B$ path way in LPS-stimulated murine macrophages. International Immunopharmacology. 2009;9:1049-57. https://doi.org/10.1016/j.intimp.2009.04.012 - Park KS, Lee SH. The Convergence of Oriental Medicine and Western Medicine on the Harmony of Eum and Yang. the Korea institute of oriental medical informatics. 2012;18:116-137.