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http://dx.doi.org/10.5941/MYCO.2015.43.3.319

Methyl 9-Oxo-(10E,12E)-octadecadienoate Isolated from Fomes fomentarius Attenuates Lipopolysaccharide-Induced Inflammatory Response by Blocking Phosphorylation of STAT3 in Murine Macrophages  

Choe, Ji-Hyun (Division of Biotechnology, Advanced Institute of Environment and Bioscience, College of Environmental & Bioresources, Chonbuk National University)
Yi, Young-Joo (Division of Biotechnology, Advanced Institute of Environment and Bioscience, College of Environmental & Bioresources, Chonbuk National University)
Lee, Myeong-Seok (Division of Biotechnology, Advanced Institute of Environment and Bioscience, College of Environmental & Bioresources, Chonbuk National University)
Seo, Dong-Won (Division of Biotechnology, Advanced Institute of Environment and Bioscience, College of Environmental & Bioresources, Chonbuk National University)
Yun, Bong-Sik (Division of Biotechnology, Advanced Institute of Environment and Bioscience, College of Environmental & Bioresources, Chonbuk National University)
Lee, Sang-Myeong (Division of Biotechnology, Advanced Institute of Environment and Bioscience, College of Environmental & Bioresources, Chonbuk National University)
Publication Information
Mycobiology / v.43, no.3, 2015 , pp. 319-326 More about this Journal
Abstract
Fomes fomentarius is a fungus of the Polyporaceae family and is used in traditional oriental therapies. Although the anti-inflammatory activities of this species have been previously reported, the identity of the bioactive compounds responsible for this activity remains unknown. Here, we investigated whether methyl 9-oxo-(10E,12E)-octadecadienoate (FF-8) purified from F. fomentarius exerts anti-inflammatory activity in murine macrophages stimulated with lipopolysaccharide (LPS). FF-8 suppressed secretion of nitric oxide (NO) and prostaglandin $E_2$ through downregulation of inducible NO synthase and cyclooxygenase-2 expression induced by LPS. In addition, pretreatment of cells with FF-8 led to a reduction in levels of secreted inflammatory cytokines such as tumor necrosis factor-${\alpha}$ and interleukin-6 in macrophages stimulated with LPS. Conversely, FF-8 did not affect nuclear factor ${\kappa}B$, p38, c-Jun NH2-terminal kinase, and extracellular signal-regulated kinase pathways. Instead, FF-8 specifically interfered with signal transducer and activator of transcription 3 (STAT3) phosphorylation induced by LPS. Collectively, this study demonstrated that FF-8 purified from F. fomentarius suppresses inflammatory responses in macrophages stimulated with LPS by inhibiting STAT3 activation. Further studies will be required to elucidate the anti-inflammatory effect of FF-8 in vivo.
Keywords
Anti-inflammatory effect; Fomes fomentarius; Macrophages; STAT3;
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1 Liaunardy-Jopeace A, Gay NJ. Molecular and cellular regulation of Toll-like receptor-4 activity induced by lipopolysaccharide ligands. Front Immunol 2014;5:473.
2 Fresno M, Alvarez R, Cuesta N. Toll-like receptors, inflammation, metabolism and obesity. Arch Physiol Biochem 2011;117:151-64.   DOI
3 Monaco C, Terrando N, Midwood KS. Toll-like receptor signaling: common pathways that drive cardiovascular disease and rheumatoid arthritis. Arthritis Care Res (Hoboken) 2011;63:500-11.   DOI
4 Fujihara M, Muroi M, Tanamoto K, Suzuki T, Azuma H, Ikeda H. Molecular mechanisms of macrophage activation and deactivation by lipopolysaccharide: roles of the receptor complex. Pharmacol Ther 2003;100:171-94.   DOI
5 Kaminska B. MAPK signalling pathways as molecular targets for anti-inflammatory therapy: from molecular mechanisms to therapeutic benefits. Biochim Biophys Acta 2005;1754:253-62.   DOI
6 Ivanenkov YA, Balakin KV, Lavrovsky Y. Small molecule inhibitors of NF-${\kappa}B$ and JAK/STAT signal transduction pathways as promising anti-inflammatory therapeutics. Mini Rev Med Chem 2011;11:55-78.   DOI
7 Saar M. Fungi in Khanty folk medicine. J Ethnopharmacol 1991;31:175-9.   DOI
8 Ito H, Sugiura M, Miyazaki T. Antitumor polysaccharide fraction from the culture filtrate of Fomes fomentarius. Chem Pharm Bull (Tokyo) 1976;24:2575.   DOI
9 Park YM, Kim IT, Park HJ, Choi JW, Park KY, Lee JD, Nam BH, Kim DG, Lee JY, Lee KT. Anti-inflammatory and anti-nociceptive effects of the methanol extract of Fomes fomentarius. Biol Pharm Bull 2004;27:1588-93.   DOI
10 Lee JS. Effects of Fomes fomentarius supplementation on antioxidant enzyme activities, blood glucose, and lipid profile in streptozotocin-induced diabetic rats. Nutr Res 2005;25:187-95.   DOI
11 Rollo F, Sassaroli S, Ubaldi M. Molecular phylogeny of the fungi of the Iceman's grass clothing. Curr Genet 1995;28:289-97.   DOI
12 Singh P, Rangaswa S. Chemical examination of Fomes fomentarius (L) Fr. Indian J Chem 1965;3:575.
13 Yokoyama A, Natori S, Aoshima K. Distribution of tetracyclic triterpenoids of lanostane group and sterols in the higher fungi especially of the polyporaceae and related families. Phytochemistry 1975;14:487-97.   DOI
14 Wolin MS. Reactive oxygen species and the control of vascular function. Am J Physiol Heart Circ Physiol 2009;296:H539-49.   DOI
15 Arpin N, Favre-Bonvin J, Steglich W. Le fomentariol: Nouvelle benzotropolone isolee de Fomes fomentarius. Phytochemistry 1974;13:1949-52.   DOI
16 Breton T, Liaigre D, Belgsir EM. Allylic oxidation: easy synthesis of alkenones from activated alkenes with TEMPO. Tetrahedron Lett 2005;46:2487-90.   DOI
17 Ferrari M, Fornasiero MC, Isetta AM. MTT colorimetric assay for testing macrophage cytotoxic activity in vitro. J Immunol Methods 1990;131:165-72.   DOI
18 Yang SH, Ahn EK, Lee JA, Shin TS, Tsukamoto C, Suh JW, Mei I, Chung G. Soyasaponins Aa and Ab exert an antiobesity effect in 3T3-L1 adipocytes through downregulation of $PPAR\gamma$. Phytother Res 2015;29:281-7.   DOI
19 Choi S, Nguyen VT, Tae N, Lee S, Ryoo S, Min BS, Lee JH. Anti-inflammatory and heme oxygenase-1 inducing activities of lanostane triterpenes isolated from mushroom Ganoderma lucidum in RAW264.7 cells. Toxicol Appl Pharmacol 2014; 280:434-42.   DOI
20 O'Callaghan YC, O'Brien NM, Kenny O, Harrington T, Brunton N, Smyth TJ. Anti-inflammatory effects of wild Irish mushroom extracts in RAW264.7 mouse macrophage cells. J Med Food 2015;18:202-7.   DOI
21 Dudhgaonkar S, Thyagarajan A, Sliva D. Suppression of the inflammatory response by triterpenes isolated from the mushroom Ganoderma lucidum. Int Immunopharmacol 2009;9:1272-80.   DOI
22 Kalinski P. Regulation of immune responses by prostaglandin E2. J Immunol 2012;188:21-8.   DOI
23 Nakanishi M, Rosenberg DW. Multifaceted roles of PGE2 in inflammation and cancer. Semin Immunopathol 2013;35:123-37.   DOI
24 Predonzani A, Cali B, Agnellini AH, Molon B. Spotlights on immunological effects of reactive nitrogen species: when inflammation says nitric oxide. World J Exp Med 2015;5:64-76.   DOI
25 Jedinak A, Dudhgaonkar S, Wu QL, Simon J, Sliva D. Antiinflammatory activity of edible oyster mushroom is mediated through the inhibition of NF-kappaB and AP-1 signaling. Nutr J 2011;10:52.   DOI
26 Zha L, Chen J, Sun S, Mao L, Chu X, Deng H, Cai J, Li X, Liu Z, Cao W. Soyasaponins can blunt inflammation by inhibiting the reactive oxygen species-mediated activation of PI3K/Akt/NF-kB pathway. PLoS One 2014;9:e107655.   DOI
27 Zhu ZG, Jin H, Yu PJ, Tian YX, Zhang JJ, Wu SG. Mollugin inhibits the inflammatory response in lipopolysaccharidestimulated RAW264.7 macrophages by blocking the Janus kinase-signal transducers and activators of transcription signaling pathway. Biol Pharm Bull 2013;36:399-406.   DOI
28 Krakauer T. Molecular therapeutic targets in inflammation: cyclooxygenase and NF-kappaB. Curr Drug Targets Inflamm Allergy 2004;3:317-24.   DOI
29 Chen W, Zhao Z, Chen SF, Li YQ. Optimization for the production of exopolysaccharide from Fomes fomentarius in submerged culture and its antitumor effect in vitro. Bioresour Technol 2008;99:3187-94.   DOI