Acknowledgement
Supported by : Jeju National University
References
- Shin T, Ahn M, Matsumoto Y. Mechanism of experimental autoimmune encephalomyelitis in Lewis rats: recent insights from macrophages. Anat Cell Biol 2012;45:141-8. https://doi.org/10.5115/acb.2012.45.3.141
- Tanuma N, Shin T, Kogure K, Matsumoto Y. Differential role of TNF-alpha and IFN-gamma in the brain of rats with chronic relapsing autoimmune encephalomyelitis. J Neuroimmunol 1999;96:73-9. https://doi.org/10.1016/S0165-5728(99)00018-1
- Matsumoto Y, Kohyama K, Aikawa Y, Shin T, Kawazoe Y, Suzuki Y, Tanuma N. Role of natural killer cells and TCR gamma delta T cells in acute autoimmune encephalomyelitis. Eur J Immunol 1998;28:1681-8. https://doi.org/10.1002/(SICI)1521-4141(199805)28:05<1681::AID-IMMU1681>3.0.CO;2-T
- Wang P, Xie K, Wang C, Bi J. Oxidative stress induced by lipid peroxidation is related with inflammation of demyelination and neurodegeneration in multiple sclerosis. Eur Neurol 2014;72:249-54. https://doi.org/10.1159/000363515
- van Horssen J, Witte ME, Schreibelt G, de Vries HE. Radical changes in multiple sclerosis pathogenesis. Biochim Biophys Acta 2011;1812:141-50. https://doi.org/10.1016/j.bbadis.2010.06.011
- Ljubisavljevic S, Stojanovic I, Pavlovic D, Sokolovic D, Stevanovic I. Aminoguanidine and N-acetyl-cysteine supress oxidative and nitrosative stress in EAE rat brains. Redox Rep 2011;16:166-72. https://doi.org/10.1179/1351000211Y.0000000007
- Lee IK, Kang JW. A check list of marine algae in Korea. Korean J Phycol 1986;1:311-25.
- Kim MM, Rajapakse N, Kim SK. Anti-inflammatory effect of Ishige okamurae ethanolic extract via inhibition of NF-kappaB transcription factor in RAW 264.7 cells. Phytother Res 2009;23:628-34. https://doi.org/10.1002/ptr.2674
- Heo SJ, Kim JP, Jung WK, Lee NH, Kang HS, Jun EM, Park SH, Kang SM, Lee YJ, Park PJ, Jeon YJ. Identification of chemical structure and free radical scavenging activity of diphlorethohydroxycarmalol isolated from a brown alga, Ishige okamurae. J Microbiol Biotechnol 2008;18:676-81.
- Zou Y, Qian ZJ, Li Y, Kim MM, Lee SH, Kim SK. Antioxidant effects of phlorotannins isolated from Ishige okamurae in free radical mediated oxidative systems. J Agric Food Chem 2008;56:7001-9. https://doi.org/10.1021/jf801133h
- Heo SJ, Cha SH, Kim KN, Lee SH, Ahn G, Kang DH, Oh C, Choi YU, Affan A, Kim D, Jeon YJ. Neuroprotective effect of phlorotannin isolated from Ishige okamurae against H2O2-induced oxidative stress in murine hippocampal neuronal cells, HT22. Appl Biochem Biotechnol 2012;166:1520-32. https://doi.org/10.1007/s12010-012-9545-7
- Ahn M, Moon C, Yang W, Ko EJ, Hyun JW, Joo HG, Jee Y, Lee NH, Park JW, Ko RK, Kim GO, Shin T. Diphlorethohydroxycarmalol, isolated from the brown algae Ishige okamurae, protects against radiation-induced cell damage in mice. Food Chem Toxicol 2011;49:864-70. https://doi.org/10.1016/j.fct.2010.12.008
- Shin T, Ahn M, Hyun JW, Kim SH, Moon C. Antioxidant marine algae phlorotannins and radioprotection: a review of experimental evidence. Acta Histochem 2014;116:669-74. https://doi.org/10.1016/j.acthis.2014.03.008
- Kim H, Moon C, Park EJ, Jee Y, Ahn M, Wie MB, Shin T. Amelioration of experimental autoimmune encephalomyelitis in Lewis rats treated with fucoidan. Phytother Res 2010;24:399-403. https://doi.org/10.1002/ptr.2959
- Ahn M, Yang W, Kim H, Jin JK, Moon C, Shin T. Immunohistochemical study of arginase-1 in the spinal cords of Lewis rats with experimental autoimmune encephalomyelitis. Brain Res 2012;1453:77-86. https://doi.org/10.1016/j.brainres.2012.03.023
- Kim J, Choi Y, Ahn M, Jung K, Shin T. Olfactory dysfunction in autoimmune central nervous system neuroinflammation. Mol Neurobiol 2018;55:8499-508. https://doi.org/10.1007/s12035-018-1001-4
- Granert C, Raud J, Lindquist L. The polysaccharide fucoidin inhibits the antibiotic-induced inflammatory cascade in experimental pneumococcal meningitis. Clin Diagn Lab Immunol 1998;5:322-4.
- Uhm CS, Kim KB, Lim JH, Pee DH, Kim YH, Kim H, Eun BL, Tockgo YC. Effective treatment with fucoidin for perinatal hypoxic-ischemic encephalopathy in rats. Neurosci Lett 2003;353:21-4. https://doi.org/10.1016/j.neulet.2003.09.013
- Mecha M, Feliu A, Machin I, Cordero C, Carrillo-Salinas F, Mestre L, Hernandez-Torres G, Ortega-Gutierrez S, Lopez-Rodriguez ML, de Castro F, Clemente D, Guaza C. 2-AG limits Theiler's virus induced acute neuroinflammation by modulating microglia and promoting MDSCs. Glia 2018;66:1447-63. https://doi.org/10.1002/glia.23317
- Li JJ, Liu SJ, Liu XY, Ling EA. Herbal compounds with special reference to gastrodin as potential therapeutic agents for microglia mediated neuroin fl ammation. Curr Med Chem 2018 Feb 14 [Epub]. https://doi.org/10.2174/0929867325666180214123929.
- Carrillo-Salinas FJ, Mestre L, Mecha M, Feliu A, Del Campo R, Villarrubia N, Espejo C, Montalban X, Alvarez-Cermeno JC, Villar LM, Guaza C. Gut dysbiosis and neuroimmune responses to brain infection with Theiler's murine encephalomyelitis virus. Sci Rep 2017;7:44377. https://doi.org/10.1038/srep44377
- Ahn M, Kang J, Lee Y, Riu K, Kim Y, Jee Y, Matsumoto Y, Shin T. Pertussis toxin-induced hyperacute autoimmune encephalomyelitis in Lewis rats is correlated with increased expression of inducible nitric oxide synthase and tumor necrosis factor alpha. Neurosci Lett 2001;308:41-4. https://doi.org/10.1016/S0304-3940(01)01979-6
- Moon C, Ahn M, Jee Y, Heo S, Kim S, Kim H, Sim KB, Koh CS, Shin YG, Shin T. Sodium salicylate-induced amelioration of experimental autoimmune encephalomyelitis in Lewis rats is associated with the suppression of inducible nitric oxide synthase and cyclooxygenases. Neurosci Lett 2004;356:123-6. https://doi.org/10.1016/j.neulet.2003.11.038
- Moon C, Ahn M, Wie MB, Kim HM, Koh CS, Hong SC, Kim MD, Tanuma N, Matsumoto Y, Shin T. Phenidone, a dual inhibitor of cyclooxygenases and lipoxygenases, ameliorates rat paralysis in experimental autoimmune encephalomyelitis by suppressing its target enzymes. Brain Res 2005;1035:206-10. https://doi.org/10.1016/j.brainres.2004.12.017
Cited by
- Natural Products and Their Bioactive Compounds: Neuroprotective Potentials against Neurodegenerative Diseases vol.2020, pp.None, 2020, https://doi.org/10.1155/2020/6565396