References
- Bendtzen K. 1988. Interleukin 1, interleukin 6 and tumor necrosis factor in infection, inflammation and immunity. Immunol Lett 19: 183-191. https://doi.org/10.1016/0165-2478(88)90141-1
- Mercurio F, Zhu H, Murray BW, Shevchenko A, Bennett BL, Li J. 1997. IKK-1 and IKK-2: cytokine-activated IkappaB kinases essential for NF-kappaB activation. Science 278: 860-866. https://doi.org/10.1126/science.278.5339.860
- Szabo C. 1995. Alterations in nitric oxide production in various forms of circulatory shock. New Horiz 3: 2-32.
- Kim AR, Cho JY, Zou Y, Choi JS, Chung HY. 2005. Flavonoids differentially modulate nitric oxide production pathways in lipopolysaccharide-activated RAW264.7 cells. Arch Pharm Res 28: 297-304. https://doi.org/10.1007/BF02977796
- Yoon S, Lee Y, Park SK, Kim H, Bae H, Kim HM, Ko S, Choi HY, Oh MS, Park W. 2009. Anti-inflammatory effects of Scutellaria baicalensis water extract on LPS-activated RAW264.7 macrophages. J Ethnopharmacol 125: 286-290. https://doi.org/10.1016/j.jep.2009.06.027
- Weinstein SL, Sanghera JS, Lemke K, DeFranco AL, Pelech SL. 1992. Bacterial lipopolysaccharide induces tyrosine phosphorylation and activation of mitogen activated protein kinases in macrophages. J Biol Chem 267: 14955-14962.
- Paul A, Cuenda A, Bryant CE, Murray J, Chilvers ER, Cohen P, Gould GW, Plevin R. 1999. Involvement of mitogen-activated protein kinase homologues in the regulation of lipopolysaccharide-mediated induction of cyclooxygenase-2 but not nitric oxide synthase in RAW 264.7 macrophages. Cell Signal 11: 491-497. https://doi.org/10.1016/S0898-6568(99)00018-2
- Murakama A. 2009. Chemoprevention with phytochemicals targeting inducibles nitric oxide synthase. Food factors for health promotion. Forum of Nutrition Basel Karger 61: 193-203. https://doi.org/10.1159/000212751
- Baeuerle PA, D Baltimore. 1996. NF-kappa B: ten years after. Cell 87: 13-20. https://doi.org/10.1016/S0092-8674(00)81318-5
- Chung WY, Part JH, Kim MJ, Kim HO, Hwang JK, Lee SK. 2007. Xanthorrhizol inhibits 12-O-tetradecanoylphorbol- 13-acetate-induced acute inflammation and twostage mouse skin carcinogenesis by blocking the expression of arnithine decarboxylase, cyclooxygenase-2 and inducible nitric oxide synthase through mitogen-activated protein kinases and/or the nuclear factor-kappa B. Carcinogenesis 28: 1224-1231. https://doi.org/10.1093/carcin/bgm005
- Meng L, Lozano YF, Gaydou EM, Li B. 2008. Antioxidant activities of polyphenols extracted from Perilla frutescens varieties. Molecules 14:133-140. https://doi.org/10.3390/molecules14010133
- Makino T, Furuta Y, Wakushima H, Fujii H, Saito K, Kano Y. 2003. Anti-allergic effect of Perilla frutescens and its active constituents. Phytother Res 17: 240-243. https://doi.org/10.1002/ptr.1115
- Ueda H, Yamazaki C, Yamazaki M. 2003. Inhibitory effect of perilla leaf extract and luteolin on mouse skin tumor promotion. Biol Pharm Bull 26: 560-563. https://doi.org/10.1248/bpb.26.560
- Kim KH, Chang MW, Park KY, Rhee SH, Rhew TH, Sunwoo YL. 1993. Antitumor activity of phytol identified from perilla leaf and its augmentative effect on cellular immune response. Korean J Nutr 26: 379-389.
- Kim GJ, Kim YG, Kim HS. 1999. Effect of Perilla frutescens extract on the lipid peroxidation enzyme activities of serum in streptozotocin-induced rats. J Agric Tech & Dev Inst 3: 1-6.
- Lee HS, Lee HA, Hong CY, Yang SY, Lee KW, Hong SY, Park SR, Lee HJ. 2009. Quantification of caffeic acid and rosmarinic acid and antioxidant activities of hot-water extracts from leaves of Perilla frutescens. Korean J Food Sci Technol 41: 302-306.
- Mosmann T. 1983. Rapid colormetric assay for cellular growth and survival application to proliferation and cytotoxicity assays. J Immunol Methods 65: 55-63. https://doi.org/10.1016/0022-1759(83)90303-4
- Leloup C, Magnan C, Benani A, Bonnet E, Alquier T, Offer G, Carriere A, Periquet A, Fernandez Y, Ktorza A, Casteilla L, Penicaud L. 2006. Mitochondrial reactive oxygen species are required for hypothalamic glucose sensing. Diabetes 55: 2084-2090. https://doi.org/10.2337/db06-0086
- Bradford MM. 1976. A rapid and sensitive method for the quantification of microgram quantities of proteins utilizing the principle of protein-dye binding. Ann Biochem 72: 248-254. https://doi.org/10.1016/0003-2697(76)90527-3
- Aebi H. 1984. Catalase in vitro. Methods Enzymol 105: 121-126. https://doi.org/10.1016/S0076-6879(84)05016-3
- Lawrence RA, Burk RF. 1976. Glutathione peroxidase activity in selenium-deficient rat liver. Biochem Biophys Res Commun 71: 952-958. https://doi.org/10.1016/0006-291X(76)90747-6
- D' Agostino P, Ferlazzo V, Milano S, La Rosa M, Di Bella G, Caruso R, Barbera C, Grimaudo S, Tolomeo M, Feo S, Cillari E. 2001. Anti-inflammatory effects of chemically modified tetracyclines by the inhibition of nitric oxide and inteleukin-12 synthesis in J774 cell line. Int Immunopharmacol 1: 1765-1776. https://doi.org/10.1016/S1567-5769(01)00100-X
- Kim EK. 2008. Purification and characterization of antioxidative peptides from enzymatic hydrolysates of venison. PhD Dissertation. Pusan National University, Busan, Korea.
- Kapp A. 1990. Reactive oxygen species and inflammation. Hautarzt 41: 196-203.
- Delaporte RH, Sanchez GM, Cuellar AC, Giuliani A, Palazzo de Mello JC. 2002. Anti-inflammatory activity and lipid peroxidation inhibition of iridoid lamiide isolated from Bouchea fluminensis (Vell.) Mold. (Verbenaceae). J Ethnopharmacol 82: 127-130. https://doi.org/10.1016/S0378-8741(02)00181-2
- Halliwell B, Hoult JR, Blake DR. 1988. Oxidants, inflammation and anti-inflammatory drugs. FASEB J 2: 2867-2873. https://doi.org/10.1096/fasebj.2.13.2844616
- Yao DC, Shi WB, Gou YL, Zhou XR, Tak YA, Zhou YK. 2005. Fatty acid-mediated intracellular iron translocation: a synergistic mechanism of oxidative injury. Free Radic Biol Med 39: 1385-1398. https://doi.org/10.1016/j.freeradbiomed.2005.07.015
- Bulkey GB. 1983. The role of oxygen free radicals in human disease processes. Surgery 94: 407-411.
- Yasui K, Baba A. 2006. Therapeutic potential of superoxide dismutase (SOD) for resolution of inflammation. Inflamm Res 55: 359-363. https://doi.org/10.1007/s00011-006-5195-y
- Benhamou PY, Moriscot C, Richard MJ. 1998. Adenovirusmediated catalase gene transcription reduces oxidant stress in human, porcine and rat pancreatic islets. Diabetologia 41: 1093-1100. https://doi.org/10.1007/s001250051035
- Itzkowitz SH, Yio X. 2004. Inflammation and cancer IV. Colorectal cancer in inflammatory bowel disease: the role of inflammation. Am J Physiol Gastrointest Liver Physiol 287: 7-17. https://doi.org/10.1152/ajpgi.00079.2004
- Krol W, Czuba ZP, Threadgill MD, Cunningham BD, Pietsz G. 1995. Inhibition of nitric oxide (NO) production in murine macrophages by flavones. Biochem Pharmacol 50: 1031-1035. https://doi.org/10.1016/0006-2952(95)00237-T
- Munhoz CD, Garcia-Bueno B, Madrigal JLM, Lepsch LB, Scavone C, Leza JC. 2008. Stress-induced neuroinflammation: mechanisms and new pharmacological targets. Bruz J Med Biol Res 41: 1037-1046. https://doi.org/10.1590/S0100-879X2008001200001
- Li XA, Everson W, Smart EJ. 2006. Nitric oxide, caveolae and vascular pathology. Cardiovasc Toxicol 6: 1-13. https://doi.org/10.1385/CT:6:1:1
- Qureshi N, Vogel SN, Van Way C, Papasian CJ, Qureshi AA, Morrison DC. 2005. The proteasome: a central regulator of inflammation and macrophage function. Immunol Res 31: 243-260. https://doi.org/10.1385/IR:31:3:243
-
Beutler B, Cerami A. 1989. The biology of cachectin/TNF-
$\alpha$ primary mediator of the host response. Annu Rev Immunol 7: 625-655. https://doi.org/10.1146/annurev.iy.07.040189.003205 - Dinarello CA. 1999. Cytokines as endogenous pyrogens. J Infect Dis 179: 294-304. https://doi.org/10.1086/314577
- Hu XD, Yang Y, Zhong XG, Zhang XH, Zhang YN, Zheng ZP, Zhou Y, Tang W, Yang YF. 2008. Anti-inflammatory effects of Z23 on LPS-induced inflammatory responses in RAW 264.7 macrophage. J Ethnopharmacol 120: 447-451. https://doi.org/10.1016/j.jep.2008.09.026
-
Lawrence T, Gilroy DW, Colville-Nash PR, Willoughby DA. 2001. Possible new role for NF-
${\kappa}B$ in the resolution of inflammation. Nat Med 7: 1291-1297. https://doi.org/10.1038/nm1201-1291 - Baldwin Jr AS. 1996. The NF-kappaB and I-kappaB proteins: newdiscoveries and insights. Annu Rev Immunol 14: 649-683. https://doi.org/10.1146/annurev.immunol.14.1.649
- Ohshima H, Bartsch H. 1994. Chronic infections and inflammatory processes as cancer risk factors: possible role of nitric oxide in carcinogenesis. Mutat Res 305: 253-264. https://doi.org/10.1016/0027-5107(94)90245-3
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