Observations of Forsythia koreana methanol extract on mast cell-mediated allergic reactions in experimental models

被引:19
作者
Choi, In-Young
Moon, Phil-Dong
Koo, Hyun-Na
Myung, Noh-Yil
Kim, Su-Jin
Lee, Ji-Hyun
Han, Se-Hee
Moon, Goo
Seo, Sung-Yum
Sung, Hyun-Jea
Park, Rae-Kil
Jeong, Hyun-Ja
Um, Jae-Young
Kim, Hyung-Min
Hong, Seung-Heon
机构
[1] Kyung Hee Univ, Inst Oriental Med, Coll Oriental Med, Dept Pharmacol, Seoul 130701, South Korea
[2] Wonkwang Univ, Res Ctr, Coll Pharm, Iksan 570749, Jeonbuk, South Korea
[3] Kyonggi Univ, Grad Sch Alternat Med, Seoul 120702, South Korea
[4] Wonkwang Univ, Coll Oriental Med, Iksan 570749, Jeonbuk, South Korea
[5] Kongju Natl Univ, Coll Nat Sci, Dept Biol, Kong Ju 314701, South Korea
关键词
anti-allergic inflammation; compound48/80; histamine; cytokines; HMC-1; cells;
D O I
10.1007/s11626-007-9040-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To explore effects of Forsythia koreana methanol extract (FKME) on mast cell-mediated allergic and inflammatory properties, the effect of FKME was evaluated on compound 48/80-induced systemic anaphylaxis, ear swelling, and anti-dinitrophenyl (DNP) immunoglobulin E (IgE)-induced passive cutaneous anaphylaxis (PCA). In addition, the effect of FKME was investigated on the histamine release from rat peritoneal mast cells (RPMCs) stimulated by compound 48/80, which promotes histamine release. The human mast cell line HMC-1 was stimulated by phorbol 12-myristate 13-acetate plus calcium ionophore A23187. Activated HMC-1 can produce several proinflammatory and chemotactic cytokines such as tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-6, and IL-8. Cytokine levels in the culture supernatant were measured by an enzyme-linked immunosorbent assay. Cytotoxicity by FKME was determined by a 3-(4,5-dimethylthiazol-2-yl)-diphenyl-tetrazolium bromide (MTT) assay. FKME inhibited compound 48/80-induced systemic anaphylactic shock and ear swelling in mice. When 1 g/kg FKME was pretreated or posttreated with mice, compound 48/80-induced mice morality was 50 and 66.7%, respectively. One gram per kilogram of FKME pretreatment inhibited ear-swelling responses derived from compound 48/80 by 29.75%. A PCA reaction was inhibited by 17.9%. In an in vitro model, FKME (1 mg/ml) inhibited histamine release from the RPMCs by 13.8% and TNF-alpha, IL-6, and IL-8 production from HMC-1 cells by 71.16% (P < 0.001), 86.72% (P < 0.001), and 44.6%, respectively. However, FKME had no cytotoxic effects on cell viability. In conclusion, FKME inhibited not only systemic anaphylaxis and ear swelling induced by compound 48/80 but also inhibited a PCA reaction induced by anti-DNP IgE in vivo. Treatment with FKME showed significant inhibitory effects on histamine, TNF-alpha, IL-6, and IL-8 release from mast cells.
引用
收藏
页码:215 / 221
页数:7
相关论文
共 44 条
[1]   Functional compartments in rat mast cells for cAMP and calcium on histamine release [J].
Alfonso, A ;
Cabado, AG ;
Vieytes, MR ;
Botana, LM .
CELLULAR SIGNALLING, 2000, 12 (05) :343-350
[2]   Interleukin 6 is required for the development of collagen-induced arthritis [J].
Alonzi, T ;
Fattori, E ;
Lazzaro, D ;
Costa, P ;
Probert, L ;
Kollias, G ;
De Benedetti, F ;
Poli, V ;
Ciliberto, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (04) :461-468
[3]   Mast cells and their mediators in cutaneous wound healing active participants or innocent bystanders? [J].
Artuc, M ;
Hermes, B ;
Steckelings, UM ;
Grützkau, A ;
Henz, BM .
EXPERIMENTAL DERMATOLOGY, 1999, 8 (01) :1-16
[4]   Interleukin 6 knock-out mice are resistant to antigen-induced experimental arthritis [J].
Boe, A ;
Baiocchi, M ;
Carbonatto, M ;
Papoian, R ;
Serlupi-Crescenzi, O .
CYTOKINE, 1999, 11 (12) :1057-1064
[5]   Immunopathology and human mast cell cytokines [J].
Bradding, P ;
Holgate, ST .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 1999, 31 (02) :119-133
[6]   CYTOKINES IN SYMPTOMATIC ASTHMA AIRWAYS [J].
BROIDE, DH ;
LOTZ, M ;
CUOMO, AJ ;
COBURN, DA ;
FEDERMAN, EC ;
WASSERMAN, SI .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 89 (05) :958-967
[7]   COMPOUND-48/80 IS A POTENT INHIBITOR OF PHOSPHOLIPASE-C AND A DUAL MODULATOR OF PHOSPHOLIPASE-A2 FROM HUMAN-PLATELET [J].
BRONNER, C ;
WIGGINS, C ;
MONTE, D ;
MARKI, F ;
CAPRON, A ;
LANDRY, Y ;
FRANSON, RC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 920 (03) :301-305
[8]   THE MOLECULAR ACTION OF TUMOR-NECROSIS-FACTOR-ALPHA [J].
CAMUSSI, G ;
ALBANO, E ;
TETTA, C ;
BUSSOLINO, F .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1991, 202 (01) :3-14
[9]  
Chahdi A, 2000, J PHARMACOL EXP THER, V292, P122
[10]   Role of cytokines in rheumatoid arthritis [J].
Feldmann, M ;
Brennan, FM ;
Maini, RN .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :397-440