최소 단어 이상 선택하여야 합니다.
최대 10 단어까지만 선택 가능합니다.
다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기Molecules a journal of synthetic chemistry and natural product chemistry, v.25 no.15, 2020년, pp.3345 -
Lim, Hyung Jin (Immunoregulatory Material Research Center, Korea Research Institute of Bioscience and Biotechnology, Jeongeup-si, Jeonbuk 56212, Korea) , Bak, Seon Gyeong (lhjin@kribb.re.kr (H.J.L.)) , Lim, Hee Ju (tsk9096@kribb.re.kr (S.G.B.)) , Lee, Seung Woong (limhj09@kribb.re.kr (H.J.L.)) , Lee, Soyoung (lswdoc@kribb.re.kr (S.W.L.)) , Ku, Sae-Kwang (sylee@kribb.re.kr (S.L.)) , Park, Sang-Ik (Immunoregulatory Material Research Center, Korea Research Institute of Bioscience and Biotechnology, Jeongeup-si, Jeonbuk 56212, Korea) , Lee, Seung-Jae (lhjin@kribb.re.kr (H.J.L.)) , Rho, Mun-Chual (tsk9096@kribb.re.kr (S.G.B.))
Chronic and excessive inflammation can destroy host organs and cause inflammatory diseases such as inflammatory bowel disease, asthma, and rheumatoid arthritis. In this study, we investigated the anti-inflammatory effects of Alpinia katsumadai seed-derived 2,3,5,22,23-pentahydroxy-2,6,10,15,19,23-he...
1. Chen L. Deng H. Cui H. Fang J. Zuo Z. Deng J. Li Y. Wang X. Zhao L. Inflammatory responses and inflammation-associated diseases in organs Oncotarget 2018 9 7204 10.18632/oncotarget.23208 29467962
2. Mogensen T.H. Pathogen recognition and inflammatory signaling in innate immune defenses Clin. Microbiol. Rev. 2009 22 240 273 10.1128/CMR.00046-08 19366914
3. Lu Y.C. Yeh W.C. Ohashi P.S. LPS/TLR4 signal transduction pathway Cytokine 2008 42 145 151 10.1016/j.cyto.2008.01.006 18304834
4. Fujioka S. Niu J. Schmidt C. Sclabas G.M. Peng B. Uwagawa T. Li Z. Evans D.B. Abbruzzese J.L. Chiao P.J. NF-κB and AP-1 connection: Mechanism of NF-κB-dependent regulation of AP-1 activity Mol. Cell. Biol. 2004 24 7806 7819 10.1128/MCB.24.17.7806-7819.2004 15314185
5. Kawai T. Akira S. Signaling to NF-κB by Toll-like receptors Trends Mol. Med. 2007 13 460 469 10.1016/j.molmed.2007.09.002 18029230
6. Schaible H.G. von Banchet G.S. Boettger M.K. Brauer R. Gajda M. Richter F. Hensellek S. Brenn D. Natura G. The role of proinflammatory cytokines in the generation and maintenance of joint pain Ann. N. Y. Acad. Sci. 2010 1193 60 69 10.1111/j.1749-6632.2009.05301.x 20398009
7. Feghali C.A. Wright T.M. Cytokines in acute and chronic inflammation Front. Biosci. 1997 2 d12 d26 9159205
8. Nikolaus S. Bauditz J. Gionchetti P. Witt C. Lochs H. Schreiber S. Increased secretion of pro-inflammatory cytokines by circulating polymorphonuclear neutrophils and regulation by interleukin 10 during intestinal inflammation Gut 1998 42 470 476 10.1136/gut.42.4.470 9616306
9. Martel-Pelletier J. Alaaeddine N. Pelletier J.P. Cytokines and their role in the pathophysiology of osteoarthritis Front. Biosci. 1999 4 d694 d703 10.2741/A387 10525480
10. Chung K.F. Barnes P.J. Cytokines in asthma Thorax 1999 54 825 857 10.1136/thx.54.9.825 10456976
11. Al-Janadi M. Al-Balla S. Al-Dalaan A. Raziuddin S. Cytokine profile in systemic lupus erythematosus, rheumatoid arthritis, and other rheumatic diseases J. Clin. Immunol. 1993 13 58 67 10.1007/BF00920636 8445045
12. Lee S.E. Shin H.T. Hwang H.J. Kim J.H. Antioxidant activity of extracts from Alpinia katsumadai seed Phytotherapy Res. 2003 17 1041 1047 10.1002/ptr.1291 14595584
13. Yang Y. Koyama K. Takahashi K. Tai T. Nunoura Y. Watanabe K. Two novel anti-emetic principles of Alpinia katsumadai J. Nat. Prod. 1999 62 1672 1674 10.1021/np990096e 10654416
14. Wang C.Y. Song Z.M. He C.L. Zhang L.Y. A constituent of Alpinia katsumadai suppresses allergic airway inflammation Phytochem. Lett. 2017 22 149 153 10.1016/j.phytol.2017.09.009
15. Yang J. Dai Y. Xia Y.F. Huang W.Z. Wang Z.T. Alpinia katsumadai hayata prevents mouse sepsis induced by cecal ligation and puncture through promoting bacterial clearance and downregulating systemic inflammation Phytother. Res. 2009 23 267 273 10.1002/ptr.2610 18844287
16. Jang H.J. Lee S.J. Lee S. Jung K. Lee S.W. Rho M.C. Acyclic Triterpenoids from Alpinia katsumadai inhibit IL-6-induced STAT3 activation Molecules 2017 22 1611 10.3390/molecules22101611
17. Taylor R.F. Bacterial triterpenoids Microbiol. Rev. 1984 48 181 10.1128/MMBR.48.3.181-198.1984 6387426
18. Ishimatsu A. Matsuura H. Sano T. Kaya K. Watanabe M.M. Biosynthesis of isoprene units in the C34 botryococcene molecule produced by Botryococcus braunii strain Bot-22 Procedia Environ. Sci. 2012 15 56 65 10.1016/j.proenv.2012.05.010
19. Choi S.Y. Lee M.H. Choi J.H. Kim Y.K. 2, 3, 22, 23-Tetrahydroxyl-2, 6, 10, 15, 19, 23-hexamethyl-6, 10, 14, 18-tetracosatetraene, an acyclic triterpenoid isolated from the seeds of Alpinia katsumadai, Inhibits Acyl-CoA: Cholesterol Acyltransferase Activity Biol. Pharm. Bull. 2012 35 2092 2096 10.1248/bpb.b12-00617 23123480
20. Murata T. Miyase T. Muregi F.W. Naoshima-Ishibashi Y. Umehara K. Warashina T. Kanou S. Mkoji G.M. Terada M. Ishih A. Antiplasmodial triterpenoids from Ekebergia capensis J. Nat. Prod. 2008 71 167 174 10.1021/np0780093 18220356
21. Teixeira E.W. Negri G. Salatino A. Stringheta P.C. Seasonal variation, chemical composition and antioxidant activity of Brazilian propolis samples Evid. -Based Complementary Altern. Med. 2010 7 10.1093/ecam/nem177 18955317
22. Rho M.C. Kim Y.K. Lee H.S. Jun C.D. Kim K. Lee S.W. Choi J.H. Song G.Y. New acyclic triterpenoids compound, and pharmaceutical composition comprising Alpinia katsumadai extract or acyclic triterpenoids compounds isolated from the same International Patent Application No. WO/2008/133387 6 11 2008
23. Farrell A.J. Blake D.R. Palmer R.M. Moncada S. Increased concentrations of nitrite in synovial fluid and serum samples suggest increased nitric oxide synthesis in rheumatic diseases Ann. Rheum. Dis. 1992 51 1219 1222 10.1136/ard.51.11.1219 1466599
24. Sano H. Hla T. Maier J.A. Crofford L.J. Case J.P. Maciag T. Wilder R.L. In vivo cyclooxygenase expression in synovial tissues of patients with rheumatoid arthritis and osteoarthritis and rats with adjuvant and streptococcal cell wall arthritis J. Clin. Investig. 1992 89 97 108 10.1172/JCI115591 1729286
25. Tripathi P. Tripathi P. Kashyap L. Singh V. The role of nitric oxide in inflammatory reactions Fems Immunol. Med. Microbiol. 2007 51 443 452 10.1111/j.1574-695X.2007.00329.x 17903207
26. Mardini I.A. FitzGerald G.A. Selective inhibitors of cyclooxygenase-2 Mol. Interv. 2001 1 30 14993336
27. Menaka K.B. Ramesh A. Thomas B. Kumari N.S. Estimation of nitric oxide as an inflammatory marker in periodontitis J. Indian Soc. Periodontol. 2009 13 75 10.4103/0972-124X.55842 20407654
28. Ricciotti E. FitzGerald G.A. Prostaglandins and inflammation Arterioscler. Thromb. Vasc. Biol. 2011 31 986 1000 10.1161/ATVBAHA.110.207449 21508345
29. Aikawa N. Cytokine storm in the pathogenesis of multiple organ dysfunction syndrome associated with surgical insults Nihon Geka Gakkai Zasshi 1996 97 771 777 8940690
30. Peresi E. Silva S.M. Calvi S.A. Marcondes-Machado J. Cytokines and acute phase serum proteins as markers of inflammatory regression during the treatment of pulmonary tuberculosis J. Bras. Pneumol. 2008 34 942 949 10.1590/S1806-37132008001100009 19099101
31. Kellum J.A. Kong L. Fink M.P. Weissfeld L.A. Yealy D.M. Pinsky M.R. Fine J. Krichevsky A. Delude R.L. Angus D.C. Understanding the inflammatory cytokine response in pneumonia and sepsis: Results of the Genetic and Inflammatory Markers of Sepsis (GenIMS) Study Arch. Intern. Med. 2007 167 1655 1663 10.1001/archinte.167.15.1655 17698689
32. Lee H.N. Shin S.A. Choo G.S. Kim H.J. Park Y.S. Kim B.S. Kim S.K. Cho S.D. Nam J.S. Choi C.S. Anti-inflammatory effect of quercetin and galangin in LPS-stimulated RAW264. 7 macrophages and DNCB-induced atopic dermatitis animal models Int. J. Mol. Med. 2018 41 888 898 29207037
35. Uesugi M. Nakajima K. Tohyama Y. Kohsaka S. Kurihara T. Nonparticipation of nuclear factor kappa B (NFκB) in the signaling cascade of c-Jun N-terminal kinase (JNK)-and p38 mitogen-activated protein kinase (p38MAPK)-dependent tumor necrosis factor alpha (TNFα) induction in lipopolysaccharide (LPS)-stimulated microglia Brain Res. 2006 1073 48 59 16457791
36. Tang X. Metzger D. Leeman S. Amar S. LPS-induced TNF-α factor (LITAF)-deficient mice express reduced LPS-induced cytokine: Evidence for LITAF-dependent LPS signaling pathways Proc. Natl. Acad. Sci. USA 2006 103 13777 13782 10.1073/pnas.0605988103 16954198
37. Zou J. Guo P. Lv N. Huang D. Lipopolysaccharide-induced tumor necrosis factor-α factor enhances inflammation and is associated with cancer Mol. Med. Rep. 2015 12 6399 6404 10.3892/mmr.2015.4243 26324337
38. Kim H.D. Cho H.R. Moon S.B. Shin H.D. Yang K.J. Park B.R. Jang H.J. Kim L.S. l Lee, H.S.; Ku, S.K. Effect of exopolymers from Aureobasidium pullulans on formalin-induced chronic paw inflammation in mice J. Microbiol. Biotechnol. 2006 16 1954 1960
해당 논문의 주제분야에서 활용도가 높은 상위 5개 콘텐츠를 보여줍니다.
더보기 버튼을 클릭하시면 더 많은 관련자료를 살펴볼 수 있습니다.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.