참고문헌
- Ito K, Hori K. Seaweed: Chemical composition and potential food uses. Food Rev. Int. 5: 101-144 (1989) https://doi.org/10.1080/87559128909540845
- Darcy-Vrillon B. Nutritional aspects of the developing use of marine macroalgae for the human food industry. Int. J. Food Sci. Nutr. 44: S23-S35 (1993)
- MacArtain P, Gill CI, Brooks M, Campbell R, Rowland IR. Nutritional value of edible seaweeds. Nutr. Rev. 65: 535-543 (2007) https://doi.org/10.1111/j.1753-4887.2007.tb00278.x
- Takamatsu S, Hodges TW, Rajbhandari I, Gerwick WH, Hamann MT, Nagle DG. Marine natural products as novel antioxidant prototypes. J. Nat. Prod. 66: 605-608 (2003) https://doi.org/10.1021/np0204038
-
Iwai K. Antidiabetic and antioxidant effects of polyphenols in brown alga Ecklonia stolonifera in genetically diabetic KK-A
$^{y}$ mice. Plant Food Hum. Nutr. 63: 163-169 (2008) https://doi.org/10.1007/s11130-008-0098-4 - Ushakova NA, Preobrazhenskaya ME, D'Incecco A, Piccoli A, Totani L, Tinari N, Morozevich GE, Berman AE, Bilan MI, Usov AI, Ustyuzhanina NE, Grachev AA, Sanderson CJ, Kelly M, Rabinovich GA, Iacobelli S, Nifantiev NE. A comparative study of the anti-inflammatory, anticoagulant, antiangiogenic, and antiadhesive activities of 9 different fucoidans from brown seaweeds. Glycobiology 17: 541-552 (2007) https://doi.org/10.1093/glycob/cwm014
- Khan MN, Cho JY, Lee MC, Kang JY, Park NG, Fujii H, Hong YK. Isolation of two anti-inflammatory and one pro-inflammatory polyunsaturated fatty acids from the brown seaweed Undaria pinnatifida. J. Agr. Food Chem. 55: 6984-6988 (2007) https://doi.org/10.1021/jf071791s
- Kang JY, Khan MN, Park NH, Cho JY, Lee MC, Fujii H, Hong YK. Antipyretic, analgesic, and anti-inflammatory activities of the seaweed Sargassum fulvellum and Sargassum thunbergii in mice. J. Ethnopharmacol. 116: 187-190 (2008) https://doi.org/10.1016/j.jep.2007.10.032
- Medeiros VP, Queiroz KC, Cardoso ML, Monteiro GR, Oliveira FW, Chavante SF, Guimaraes LA, Rocha HA, Leite EL. Sulfated galactofucan from Lobophora variegata: Anticoagulant and antiinflammatory properties. Biochemistry -Moscow+ 73: 1018-1024 (2008) https://doi.org/10.1134/S0006297908090095
- Kim MS, Kim JY, Choi WH, Lee SS. Effects of seaweed supplementation on blood glucose concentration, lipid profile, and antioxidant enzyme activities in patients with type 2 diabetes mellitus. Nutr. Rep. Rev. 2: 62-67 (2008) https://doi.org/10.4162/nrp.2008.2.2.62
- Wang H, Ooi EV, Ang PO. Antiviral activities of extracts from Hong Kong seaweeds. J. Zhejiang Univ. Sci. B. 9: 969-976 (2008) https://doi.org/10.1631/jzus.B0820154
- Lee SB, Lee JY, Song DG, Pan CH, Nho CW, Kim MC, Lee EH, Jung SH, Kim HS, Kim YS, Um BH. Cancer chemopreventive effects of Korean seaweed extracts. Food Sci. Biotechnol. 17: 613-622 (2008)
- Green LC, Wagner DA, Glogowski J, Skipper PL, Wishnok JS, Tannenbaum SR. Analysis of nitrate, nitrite, and [15N]nitrate in biological fluids. Anal. Biochem. 126: 131-138 (1982) https://doi.org/10.1016/0003-2697(82)90118-X
- Wang HQ, Smart RC. Overexpression of protein kinase C-alpha in the epidermis of transgenic mice results in striking alterations in phorbol ester-induced inflammation and COX-2, MIP-2, and TNFalpha expression but not tumor promotion. J. Cell Sci. 112: 3497-3506 (1999)
- Arend WP, Dayer JM. Inhibition of the production and effects of interleukin-1 and tumor necrosis factor alpha in rheumatoid arthritis. Arthritis Rheum. 38: 151-160 (1995) https://doi.org/10.1002/art.1780380202
- Feldmann M, Brennan FM, Maini RN. Role of cytokines in rheumatoid arthritis. Annu. Rev. Immunol. 14: 397-440 (1996) https://doi.org/10.1146/annurev.immunol.14.1.397
- Brennan FM, Maini RN, Feldmann M. Role of pro-inflammatory cytokines in rheumatoid arthritis. Springer Semin. Immun. 20: 133-147 (1998) https://doi.org/10.1007/BF00832003
- Hewett JA, Roth RA. Hepatic and extrahepatic pathobiology of bacterial lipopolysaccharides. Pharmacol. Rev. 45: 382-411 (1993)
- Kubes P, McCafferty DM. Nitric oxide and intestinal inflammation. Am. J. Med. 109: 150-158 (2000) https://doi.org/10.1016/S0002-9343(00)00480-0
-
Donadelli R, Abbate M, Zanchi C, Corna D, Tomasoni S, Benigni A, Remuzzi G, Zoja C. Protein traffic activates NF-
$\kappa$ B gene signaling and promotes MCP-1-dependent interstitial inflammation. Am. J. Kidney Dis. 36: 1226-1241 (2000) https://doi.org/10.1053/ajkd.2000.19838 -
Ray A, Siegel MD, Prefontaine KE, Ray P. Anti-inflammation: Direct physical association and functional antagonism between transcription factor NF-
$\kappa$ B and the glucocorticoid receptor. Chest 107: 139S (1995) https://doi.org/10.1378/chest.107.3_Supplement.139S -
Giuliani C, Napolitano G, Bucci I, Montani V, Monaco F. NF-
$\kappa$ B transcription factor: Role in the pathogenesis of inflammatory, autoimmune, and neoplastic diseases and therapy implications. Clin. Ther. 152: 249-253 (2001) -
Notarbartolo M, Poma P, Perri D, Dusonchet L, Cervello M, D'Alessandro N. Antitumor effects of curcumin, alone or in combination with cisplatin or doxorubicin, on human hepatic cancer cells. Analysis of their possible relationship to changes in NF-
$\kappa$ B activation levels and in IAP gene expression. Cancer Lett. 224: 53-65 (2005) https://doi.org/10.1016/j.canlet.2004.10.051 - Karin M. The beginning of the end: IkappaB kinase (IKK) and NFkappaB activation. J. Biol. Chem. 274: 27339-27342 (1999) https://doi.org/10.1074/jbc.274.39.27339
- Dinarello CA. Biologic basis for interleukin-1 in disease. Blood 87: 2095-2147 (1996)
- Dinarello CA, Thompson RC. Blocking IL-1: interleukin 1 receptor antagonist in vivo and in vitro. Immunol. Today 12: 404-410 (1991) https://doi.org/10.1016/0167-5699(91)90142-G
- Reznikov LL, Kim SH, Westcott JY, Frishman J, Fantuzzi G, Novick D, Rubinstein M, Dinarello CA. IL-18 binding protein increases spontaneous and IL-1-induced prostaglandin production via inhibition of IFN-gamma. P. Natl. Acad. Sci. USA 97: 2174-2179 (2000) https://doi.org/10.1073/pnas.040582597
- Ahsan S, Lacey M, Whitehead SA. Interactions between interleukin-1 beta, nitric oxide, and prostaglandin E2 in the rat ovary: Effects on steroidogenesis. Eur. J. Endocrinol. 137: 293-300 (1997) https://doi.org/10.1530/eje.0.1370293
- Ellman C, Corbett JA, Misko TP, McDaniel M, Beckerman KP. Nitric oxide mediates interleukin-1-induced cellular cytotoxicity in the rat ovary. A potential role for nitric oxide in the ovulatory process. J. Clin. Invest. 92: 3053-3056 (1993) https://doi.org/10.1172/JCI116930
- Lawrence T, Gilroy DW, Colville-Nash PR, Willoughby DA. Possible new role for NF-kappaB in the resolution of inflammation. Nat. Med. 7: 1291-1297 (2001) https://doi.org/10.1038/nm1201-1291
- Renard P, Raes M. The proinflammatory transcription factor NFkappaB: A potential target for novel therapeutical strategies. Cell. Biol. Toxicol. 15: 341-344 (1999) https://doi.org/10.1023/A:1007652414175
- Barnes PJ, Karin M. Nuclear factor-kappaB: A pivotal transcription factor in chronic inflammatory diseases. New Engl. J. Med. 336: 1066-1071 (1997) https://doi.org/10.1056/NEJM199704103361506
- Makarov SS. NF-kappaB as a therapeutic target in chronic inflammation: Recent advances. Mol. Med. Today 6: 441-448 (2000) https://doi.org/10.1016/S1357-4310(00)01814-1
- Zhang G, Ghosh S. Molecular mechanisms of NF-kappaB activation induced by bacterial lipopolysaccharide through Toll-like receptors. J. Endotoxin Res. 6: 453-457 (2000)
- Takaoka A, Yanai H. Interferon signalling network in innate defence. Cell Microbiol. 8: 907-922 (2006) https://doi.org/10.1111/j.1462-5822.2006.00716.x