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1 KOREAN J. FOOD SCI. TECHNOL. Vol. 41, No. 6, pp. 717~721 (2009) š w» z ÁyÁy»ÁÁ 1 * w tƒœw, 1 w m y l The Korean Society of Food Science and Technology Anti-allergic Effect of Zizania latifolia Turcz Extracts Eun-Jung Lee, Eun-Yeong Whang, Key Whang, In-Seon Lee, and Seun-Ah Yang 1 * Deptartment of Food and Technology, Keimyung University 1 The Center for Traditional Microorganism Resources, Keimyung University Abstract The anti-allergic effect of the methanol extract of Zizania latifolia Turcz was investigated. Methanol extract of Z. latifolia Trucz did not display any cytotoxicity activities in the IgE-sensitized RBL-2H3 cells. The extract was found to inhibit compound 48/80-induced degranulation and antigen-induced β-hexosaminidase release as well as PMA plus A23187-induced TNF-α production in RBL-2H3 mast cells in a dose-dependent manner. Release of β-hexosaminidase, a marker for the release of histamine in mast cells, was inhibited with an IC 50 value of 73.8 µg/ml. These results suggest that Z. latifolia extracts may be useful for the prevention of type I allergic reaction. Key words: Zizania latifolia Turcz, β-hexosaminidase, degranulation, TNF-α, RBL-2H3 cells» y x y, y y w w w wš, ù» y y ƒ w ã ƒwš.»» w x, wx x j 4ƒ x(i~iv) ù m» w w w w w w w w z ü ù x 1x» w,», mv v»» y 1x» (type I allergic reaction) w(1-3). s x» w v s (4). s t xw š šey IgE FceRI IgE p ww, s ü e ƒ wš k ù kù xq, ƒwz š interleukin- 4(IL-4), IL-6, IL-13, TNF-α ƒ me w, x jš, x n ƒj,» j (5-8). s yy w IgE mw w w compound 48/80, protein kinase *Corresponding author: Seun-Ah Yang, The Center for Traditional Microorganism Resources, Keimyung University, Daegu , Korea Tel: Fax: seunahy@kmu.ac.kr Received August 3, 2009; revised August 21, 2009; accepted September 8, 2009 C(PKC) activator phorbol 12-myristate 13-acetate(PMA), calcium ionophore(a23187) w» š (9-11). Rat RBL-2H3 s t IgE sww, IgE z w w k w(12), w» z RBL-2H3 sƒ s š. w w w k w e (13-15).» k w,» ƒwš x w w z yw š. x w»,,,, ù (16-20). š(zizania latifolia) ù, ƒ w w t, t š. š, šx, t,,,, y ƒ ù zƒ, j z jš šš. w, ù, ywt ƒ t ù z š w(21,22). ù w š z w ù, z t ƒš. s y g t w s, DNA fragmentation s š y w w šƒ, š zšƒ ƒƒ w wvz ƒ ƒ š(23,24). š w w» w» w, RBL- 717
2 718 w twz 41 «6y (2009) 2H3 s w s yy w wz mw. x š(zizania latifolia) w k w. 100 g 30 k ƒw 24 e wš, 3z w. (Whatman No. 3, Maidstone, England) w rotary vacuum evaporator(ut-1000, EYELA, Tokyo, Japan) w z w 15.4 g, 20 o C w w. s w RBL-2H3(KCLB No ) s Rat y» s Korea Cell Line Bank(Seoul, Korea) l, 10% fetal bovine serum 1% streptomycin/ penicillin w MEM w 37 o C, 5% CO 2 w w. s d IgE s w š MTT assay dw. RBL-2H3 s( cells/well) 450 ng/ml DNP-specific IgE(Sigma, St. Louis, MO, USA) w 37 o C, 5% CO 2 w w z ( µg/ml) š s w. 12 z ƒ well 5 mg/ml MTT 10 µl ƒwš 4 37 o C incubator w. wš 100 µl DMSO well formazan wg ELISA reader(spectra MAX 340 pc, Molecular Device, Sunnyvale, CA, USA) w 550 nm Ÿ dw. s Ÿ Ÿ w ù kü. RBL-2H3 s k RBL-2H3 s 24-well plate( cells/well) 4 w z, 200 µl incubation buffer(119 mm NaCl, 5 mm KCl, 0.4 mm MgCl 2, 25 mm PIPES, 40 mm NaOH, 5.6 mm glucose, 1 mm CaCl 2, 0.1% bovine serum albumin, ph 7.2) š 10 w. 0.1% DMSO ù 25 µl ƒ ƒ 37 o C 10 g. z, compound 48/80 (Sigma) 25 µl ƒw 20, 40 g. z, s xk x (DM IRE2, Leica, Wetzlar, Germany) 600 w w. 200 w k yw, 3z x x yw. β-hexosaminidase d RBL-2H3 s( cells/well) 450 ng/ml IgE wì CO 2 incubator 12 w s g. k s siraganian buffer(119 mm NaCl, 5 mm KCl, 0.4 mm MgCl 2, 25 mm PIPES, 40 mm NaOH, ph 7.2) w z, ƒ well 160 µl siraganian buffer(119 mm NaCl, 5 mm KCl, 0.4 mm MgCl 2, 25 mm PIPES, 40 mm NaOH, 5.6 mm glucose, 1 mm CaCl 2, 0.1% bovine serum albumin, ph 7.2) š 20 w. ƒ 5µM wortmannin(wako Pure Chemical Industries, Tokyo, Japan) 10 jš, 10 µg/ml DNP-BSA(Alpha Diagnostic International, San Antonio, TX, USA) ƒw z 10 w s yy g ice bath g. d 25 µl 96-well plate»š, substrate buffer(p-nitrophenyl-n-acetyl-β-d-glucosaminide 1 mm in citrate buffer 0.1 M, ph4.5) 25 µl z 37 o C 1 g. z, ƒ well stop solution (0.1 M Na 2 CO 3 /NaHCO 3, ph 10) 200 µl ƒw jš, ELISA reader w 405 nm Ÿ dw. TNF-α d RBL-2H3 s 24-well plate( cells/well) w z 12 w. MEM w š, A23187(1 µm) PMA(50 ng/ml) w 4 w. óù z d w 70 o C w ƒ TNF-α ELISA kit(invitrogen Corporation, CA, USA) w dw. ELISA reader w 450 nm Ÿ dw TNF-α w. m w š x w m Student s t-test w. m z p 0.05 (p<0.05) m š qw. š š s IgE RBL-2H3 s w š w» w MTT assay ww, Fig. 1 ùkü. s w x s ùkü. š x µg/ml 12 w s ùkü. s k w š z Compound 48/80 formaldehyde w cross-linked phenethylamine mixed polymer s w s e s ü g s ü e ƒg s k w(25,26). Compound 48/80 w s xk x ùx s wš, ñ t, compound 48/80 yy k ù s xk s wš j»ƒ, s ü ù s (Fig. 2). Compound 48/80 w š w, k ù s xk yƒ, compound 48/80 w ü s ƒƒ ³ew st w. w, µg/ml š w compound 48/80 w s k xw w.
3 š w» z 719 Fig. 1. Cytotoxic effects of Zizania latifolia extract on RBL-2H3 cells. RBL-2H3 cells ( cells) were cultured with 450 ng/ml of DNP-specific IgE overnight. After treatment with varying doses of Z. latifolia extract, cells were cultured for 12h. The cytotoxicity of Z. latifolia extract on RBL-2H3 cells was determined by MTT assay. The value represents mean±sd of three different experiments. β-hexosaminidase w š z sƒ wwš k tryptase w» w w w w w yw w (27). β-hexosaminidase sƒ w yy k wì s k t š (28,29). RBL-2H3 s β-hexosaminidase y dw, š w β-hexosaminidase z w. 10, 20, 50, 100 µg/ml š s β- hexosaminidase y w ƒƒ 97, 77, 58, 37% ùkü, w yw (Fig. 3), IC µg/ml ùkû. w, 2.14 µg/ml wortmannin 29% ùkü β-hexosaminidase w g yw. Fig. 3. Inhibitory effects of Zizania latifolia extract on β- hexosaminidase release from RBL-2H3 cells induced by IgE with DNP-BSA. RBL-2H3 cells ( cells) were sentitized with 450 ng/ml of DNP-specific IgE overnight and pretreated with varying doses of Z. latifolia extract for 10 min. Cells were stimulated with 10 µg/ml of DNP-BSA for 10 min. The degranulation was determined by measurement of the activity of β-hexosaminidase in culture media. The value represents mean±sd of three different experiments. Wortmannin (WM, 2.14 µg/ml) was used as a positive control. *Values are significantly different from control (*p<0.05, **p<0.01). š TNF-α z TNF-α s s w,» w w w (30). š y y sl me TNF-α g ELISA w. RBL- 2H3 s TNF-α w 5.06 pg/ml û, A23187 PMA w pg/ml x ƒ yw. 10, 50, Fig. 2. Light microphotographs using inverted microscopy (magnification; 600) of RBL-2H3 cells without (1, 2, 3) or with (4, 5, 6) treatment of 50 µg/ml compound 48/80 for 40 min. The Z. latifolia extract were pretreated for 10 min (2, 5: 100 µg/ml, 3, 6: 50 µg/ml) prior to the stimulation with compound 48/80. Arrow shows degranulated cells.
4 720 w twz 41 «6y (2009) Fig. 4. Effects of Zizania latifolia extract on PMA plus A induced cytokine production in RBL-2H3 cells. The RBL-2H3 cells ( cells) were incubated overnight in 24-well plate. The cells were pretreated with various concentrations of Z. latifolia extract and then stimulated with PMA (50 ng/ml) plus A23187 (1 µm) for 4 h. The level of cytokine in the supernatant was measured by using ELISA. The value represents the mean±sd of three independent experiments. Luteolin (1.43 µg/ml) was used positive control. *Values are significantly different from control (*p<0.05, **p<0.01). 100 µg/ml š w ƒƒ 79.76, 65.38, 53.4 pg/ml d, A23187 PMA w w 91.5, 75, 61.3% g ùkù TNF-α g yw. w, 1.43 µg/ml luteolin TNFα 32.5 pg/ml ùkù w 37.3% yw (Fig. 4). s šey IgE ww w xw s adenylate cyclaseƒ yy camp ƒj, camp y protein kinase yyjš, yy protein kinase e n y g qjš s w g k w (31). w, s MAPK ERK yj NF-κB yyg TNF-α, IL-6, IL-8 me x ƒk(32). x w» zƒ š polyphenol curcumin(33), flavonoid natsudaidain(34), šp xanthone mangostin (35), ù sesquiterpene lactone(18) saponin (19). ù x š w w» z ùkü d w». š k z w» w» w šl w» y ƒ wš, w s ü y» e w w w vƒ ƒ. š k w» y w» w, s RBL-2H3 s w, š w z IgE-w, A23187 PMA w s yy g β-hexosaminidase, TNF-α dw. š yy s β-hexosaminidase, TNF-α w yw. w, s k w ùkù xkw y w w w» w š w s compound 48/80 w, š w w k x w. š w w s k w mw» j q, š w»» ƒ w. t» w m y l w. 1. Patterson R, Dykewicz MS, Grammer LC, Greenberger PA, Lawrence ID, Walker CL, Wong S, Zeiss CR. Classification of immediate-type, life-threatening allergic or pseudoallergic reactions. Chest 98: (1990) 2. Coombs, RRA, Gell, PGH. Classification of Allergic Reactions Responsible for Clinical Hypersensitivity and Disease. Clinical Aspects of Immunology, 3 rd ed. Blackwell Scientific Publications, London, UK. pp (1975) 3. Siraganian RP, Hook WA, Levine BB. Specific in vitro histamine release from basophils by bivalent haprens: The evidence for activation by simple bridging of membrane bound antibody. Immunochemistry 12: (1975) 4. Ahn KM. Role of mast cells in allergic inflammation and innate immunity. Korean J. Pediatr. 47: (2004) 5. Schroeder JT, Kagey-Sobotka A, Lichtenstein LM. The role of the basophil in allergic inflammation. Allergy 50: (1995) 6. Beaven MA, Rogers J, Moore JP, Hesketh TR, Smith GA, Metcalfe JC. The mechanism of the calcium signal and correlation with histamine release in 2H3 cells. J. Biol. Chem. 259: (1984) 7. Shakoory B, Fitzgerald SM, Lee SA, Chi DS, Krishnaswamy G. The role of human mast cell-derived cytokines in eosinophil biology. J. Interf. Cytok. Res. 245: (2004) 8. Salamon P, Shoham NG, Gavrieli R, Wolach B, Mekori YA. Human mast cells release interleukin-8 and induce neutrophil chemotaxis on contact with activated T cells. Allergy 60: (2005) 9. Metcalfe DD, Kaliner M, Donlon MA. The mast cell. Crit. Rev. Immunol. 3: (1981) 10. Chand N, Pillar J, Diamantis W, Perhach JL, Sophia RD. Inhibition of calcium ionophore (A23187) stimulated histamine release from rat peritoneal mast cells by azelastine: Implications for its mode of action. Eur. J. Pharmacol. 96: (1983) 11. Takei M, Umeyama A, Shoji N, Arihara S, Endo K. Mechanism of inhibition of IgE-dependent histamine release from rat mast x
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