Fig. 1. Effects of EF-2001 on nitric oxide in LPS activated RAW 264.7 cells.
Fig. 2 Effects of EF-2001 on cell viability in RAW 264.7 cells.
Fig. 3. Inhibition of LPS-induced iNOS and COX-2 expression by EF-2001.
Fig. 4. Effect of EF-2001 on the LPS-induced MAP kinase pathway in Raw 264.7 cells.
Fig. 5. Effect of EF-2001 on LPS-induced phosphorylation of Akt in Raw 264.7 cells.
Fig. 6. Effect of EF-2001 on LPS-induced phosphorylation of IκB in Raw 264.7 cells.
Fig. 7. Effect of EF-2001 on LPS-induced translocation of p65 in Raw 264.7 cells.
참고문헌
- Ambs, S., Hussain, S. P. and Harris, C. C. 1997. Interactive effects of nitric oxide and the p53 tumor suppressor gene in carcinogenesis and tumor progression. FASEB J. 11, 443-448. https://doi.org/10.1096/fasebj.11.6.9194524
- Bae, N. Y., Kim, M. J., Kim, K. B. W. R., Park, J. H., Park, S. H., Sung, N. Y., Byun, E. H. and Ahn, D. H. 2016. Anti-Inflammatory effect of Chondrus ocellatus Holmes ethanol extract on lipopolysaccharide-induced inflammatory responses in RAW 264.7 cells. J. Microbiol. Biotechnol. 44, 268-277.
-
Carter, A. B., Knudtson, K. L., Monick, M. M. and Hunninghake, G. W. 1999. The p38 mitogen-activated protein kinase is required for NF-
${\kappa}B$ -dependent gene expression: the role of TATA-binding protein (TBP). J. Biol. Chem. 274, 30858-30863. https://doi.org/10.1074/jbc.274.43.30858 - Cheon, J. M., Kim, H. S., Choi, E. O., Kwon, D. H., Choi, Y. H., Kim, B. W. and Hwang, H. J. 2017. Anti-inflammatory Activities of an Ethanol Extract of Sargassum macrocarpum in Lipopolysaccharide (LPS)-stimulated RAW 264.7 Macrophages. J. Life Sci. 27, 1437-1444.
- Choi, E. J., Iwasa, M., Han, K. I., Kim, W. J., Tang, Y., Hwang, Y. J., Chae, J. R., Han, W. C., Shin, Y. S. and Kim, E. K. 2016. Heat-killed Enterococcus faecalis EF-2001 ameliorates atopic dermatitis in a murine model. Nutrients 8, 146. https://doi.org/10.3390/nu8030146
- Choi, E. J., Iwasa, M., Han, K. I., Kim, W. J., Tang, Y., Han, W. C., Kim, E. K. and Park, Z. Y. 2016. Effect of Enterococcus faecalis EF-2001 on experimentally induced atopic eczema in mice. Food Sci. Biotechnol. 25, 1087-1093. https://doi.org/10.1007/s10068-016-0175-7
- Duerksen-Hughes, P. J., Day, D. B., Laster, S. M., Zachariades, N. A., Aquino, L. and Gooding, L. R. 1992. Both tumor necrosis factor and nitric oxide participate in lysis of simian virus 40-transformed cells by activated macrophages. J. Immunol. 149, 2114-2122.
-
Ghosh, S., May, M. J. and Kopp, E. B. 1998. NF-
${\kappa}B$ and REL proteins: evolutionarily conserved mediators of immune responses. Annu. Rev. Immunol. 16, 225-260. https://doi.org/10.1146/annurev.immunol.16.1.225 - Fisher, K. and Phillips, C. 2009. The ecology, epidemiology and virulence of Enterococcus. Microbiology 155, 1749-1757. https://doi.org/10.1099/mic.0.026385-0
- Funk, C. D. 2001. Prostaglandins and leukotrienes: advances in eicosanoid biology. Science 294, 1871-1875. https://doi.org/10.1126/science.294.5548.1871
- Greenhough, A., Smartt, H. J., Moore, A. E., Roberts, H. R., Williams, A. C., Paraskeva, C. and Kaidi, A. 2009. The COX-2/PGE 2 pathway: key roles in the hallmarks of cancer and adaptation to the tumour microenvironment. Carcinogenesis 30, 377-386. https://doi.org/10.1093/carcin/bgp014
-
Islam, S., Hassan, F., Tumurkhuu, G., Ito, H., Koide, N., Mori, I., Yoshida, T. and Yokochi, T. 2007. 5-Fluorouracil prevents lipopolysaccharide-induced nitric oxide production in RAW 264.7 macrophage cells by inhibiting Akt-dependent nuclear factor-
${\kappa}B$ activation. Cancer Chemother. Pharmacol. 59, 227-233. - Janicke, H., Taylor, P. M. and Bryant, C. E. 2003. Lipopolysaccharide and interferon gamma activate nuclear factor kappa B and induce cyclo-oxygenase-2 in equine vascular smooth muscle cells. Res. Vet. Sci. 75, 133-140. https://doi.org/10.1016/S0034-5288(03)00073-0
-
Kim, S. J., Park, H. J., Shin, H. J., Kim, J. S., Ahn, H. J., Min, I. S. and Youn, H. S. 2011. The effects of phenethyl isothiocyanate on nuclear factor-
${\kappa}B$ activation and cyclooxygenase-2 and inducible nitric oxide synthase expression induced by toll-like receptor agonists. J. Appl. Biol. Chem. 54, 279-283. https://doi.org/10.3839/jabc.2011.045 -
Kim, S. Y., Jo, M. J., Hwangbo, M., Back, Y. D., Jeong, T. Y., Cho, I. J. and Jee, S. Y. 2013. Anti-inflammatory effect of Stevia rebaudiana as a result of NF-
${\kappa}B$ and MAPK inhibition. J. Kor. Med. Opthalmol. Otolaryngol. Dermatol. 26, 54-64. https://doi.org/10.6114/jkood.2013.26.3.054 - Kwon, M. S., Mun, O. J., Bae, M. J., Lee, S. G., Kim, M., Lee, S. H., Yu, K. H., Kim, Y. Y. and Kong, C. S. 2015. Anti-inflammatory activity of ethanol extracts from Hizikia fusiformis fermented with lactic acid bacteria in LPS-stimulated RAW264.7 macrophages. Prev. Nutr. Food Sci. 44, 1450-1457.
- Lee, H. N., Lim, D. Y., Lim, S. S., Kim, J. D. and Yoon, J. H. 2011. Anti-inflammatory effect of ethanol extract from Eupatorium japonicum. Kor. J. Food Sci. Technol. 43, 65-71. https://doi.org/10.9721/KJFST.2011.43.1.065
- Lee, S. J. and Lim, K. T. 2009. Inhibitory effect of ZPDC glycoprotein on the expression of inflammation-related cytokines through p38 MAP kinase and JNK in lipopolysaccharide-stimulated RAW 264.7 cells. Inflamm. Res. 58, 184-191. https://doi.org/10.1007/s00011-008-8118-2
-
Limtrakul, P., Yodkeeree, S., Pitchakarn, P. and Punfa, W. 2016. Anti-inflammatory effects of proanthocyanidin-rich red rice extract via suppression of MAPK, AP-1 and NF-
${\kappa}B$ pathways in Raw 264.7 macrophages. Nutr. Res. Pract. 10, 251-258. https://doi.org/10.4162/nrp.2016.10.3.251 -
Luo, Y., Liu, M., Yao, X., Xia, Y., Dai, Y., Chou, G. and Wang, Z. 2009. Total alkaloids from Radix linderae prevent the production of inflammatory mediators in lipopolysaccharide-stimulated RAW 264.7 cells by suppressing NF-
${\kappa}B$ and MAPKs activation. Cytokine 46, 104-110. https://doi.org/10.1016/j.cyto.2008.12.017 - Murosaki, S., Yamamoto, Y., Ito, K., Inokuchi, T., Kusaka, H., Ikeda, H. and Yoshikai, Y. 1998. Heat-killed Lactobacillus plantarum L-137 suppresses naturally fed antigen-specific IgE production by stimulation of IL-12 production in mice. J. Allergy Clin. Immnol. 102, 57-64. https://doi.org/10.1016/S0091-6749(98)70055-7
-
Oh, J. H., Kang, L. L., Ban, J. O., Kim, Y. H., Kim, K. H., Han, S. B. and Hong, J. T. 2009. Anti-inflammatory effect of 4-O-methylhonokiol, a novel compound isolated from Magnolia officinalis through inhibition of NF-
${\kappa}B$ . Chem. Biol. Interact. 180, 506-514. https://doi.org/10.1016/j.cbi.2009.03.014 - Ou, C. C., Lin, S. L., Tsai, J. J. and Lin, M. Y. 2011. Heat-killed lactic acid bacteria enhance immunomodulatory potential by skewing the immune response toward Th1 polarization. J. Food Sci. 76, 260-267. https://doi.org/10.1111/j.1750-3841.2011.02161.x
- Huang, X., Chen, L. Y., Doerner, A. M., Pan, W. W., Smith, L., Huang, S., Papadimos, T. J. and Pan, Z. K. 2009. An atypical protein kinase C (PKC zeta) plays a critical role in lipopolysaccharide-activated NF-kappa B in human peripheral blood monocytes and macrophages. J. Immunol. 182, 5810-5815. https://doi.org/10.4049/jimmunol.0804073
- Qiaowen, X. and Carl, N. 1994. The high-output nitric oxide pathway: role and regulation. J. Leukocyte Biol. 56, 576-582. https://doi.org/10.1002/jlb.56.5.576
- Reddy, D. B. and Reddanna, P. 2009. Chebulagic acid (CA) attenuates LPS-induced inflammation by suppressing NF-kB and MAPK activation in RAW 264.7 macrophages. Biochem. Biophys. Res. Commun. 381, 112-117. https://doi.org/10.1016/j.bbrc.2009.02.022
- Satonaka, K., Ohashi, K., Nohmi, T., Yamamoto, T., Abe, S., Uchida, K. and Yamaguchi, H. 1996. Prophylactic effect of Enterococcus faecalis FK-23 preparation on experimental candidiasis in mice. Microbiol. Immunol. 40, 217-222. https://doi.org/10.1111/j.1348-0421.1996.tb03337.x
- Suresh Babu, C. V., Babar, S. M. E., Song, E. J., Oh, E. and Yoo, Y. S. 2008. Kinetic analysis of the MAPK and PI3K/Akt signaling pathways. Mol. Cell. 25, 397-406.
- Takeda, K. and Akira, S. 2004. TLR signaling pathways. Semin. Immnol. 16, 3-9. https://doi.org/10.1016/j.smim.2003.10.003
-
Tamir, S. and Tannenbaum, S. R. 1996. The role of nitric oxide (
$NO{\cdot}$ ) in the carcinogenic process. BBA Rev. Cancer 1288, F31-F36. - Yanagisawa, T., Gu, Y. H., Tsuchihashi, E., Umekawa, M., Yamamoto, H., Iwasa, T. and Suzuki, I. 2000. Analgesic and anti-neoplastic effects of the immunization-active fraction of Enterococcus faecalis 2001. J. Orient. Med. 5, 97-102.