Curine inhibits mast cell-dependent responses in mice

被引:19
作者
Ribeiro-Filho, Jaime [1 ]
Leite, Fagner Carvalho [4 ]
Costa, Hermann Ferreira [4 ]
Calheiros, Andrea Surrage [1 ]
Torres, Rafael Carvalho [2 ]
de Azevedo, Carolina Trindade [2 ]
Martins, Marco Aurelio [2 ]
Dias, Celidarque da Silva [3 ]
Bozza, Patricia T. [1 ]
Piuvezam, Marcia Regina [4 ]
机构
[1] Fiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, Brazil
[2] Fiocruz MS, Inst Oswaldo Cruz, Lab Inflamacao, BR-21045900 Rio De Janeiro, Brazil
[3] Univ Fed Paraiba, Dept Ciencias Farmaceut, Lab Fitoquim, Joao Pessoa, Paraiba, Brazil
[4] Univ Fed Paraiba, Dept Fisiol & Patol, Lab Imunofarmacol, Joao Pessoa, Paraiba, Brazil
关键词
Curine; Chondrodentron platyphyllum; Anti-allergic; Mast cell; Lipid mediators; SCRATCHING BEHAVIOR; HISTAMINE; RECEPTORS; ASTHMA; PATHOPHYSIOLOGY; DEGRANULATION; INVOLVEMENT; ACTIVATION; MECHANISMS; EXOCYTOSIS;
D O I
10.1016/j.jep.2014.06.041
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Curine is a bisbenzylisoquinoline alkaloid and the major constituent isolated from Chondrodendron platyphyllum, a plant that is used to treat inflammatory diseases in Brazilian folk medicine. This study investigates the effectiveness of curine on mast cell-dependent responses in mice. Materials and methods: To induce mast cell-dependent responses, Swiss mice were subcutaneously sensitized with ovalbumin (OVA-12 mu g/mouse) and Al(OH)(3) in a 0.9% NaCl solution. Fifteen days later, the animals were challenged with OVA through different pathways. Alternatively, the animals were injected with compound 48/80 or histamine, and several parameters, including anaphylaxis, itching, edema and inflammatory mediator production, were analyzed. Promethazine, cromoglycate, and verapamil were used as control drugs, and all of the treatments were performed 1 h before the challenges. Results: Curine pre-treatment significantly inhibited the scratching behavior and the paw edema induced by either compound 48/80 or OVA, and this protective effect was comparable in magnitude with those associated with treatment with either cromoglycate or verapamil. In contrast, curine was a weak inhibitor of histamine-induced paw edema, which was completely inhibited by promethazine. Curine and verapamil significantly inhibited pleural protein extravasations and prostaglandin D-2 (PGD(2)) and cysteinyl leukotrienes (CysLTs) production following allergen-induced pleurisy. Furthermore, like verapamil, curine inhibited the anaphylactic shock caused by either compound 48/80 or an allergen. In in vitro settings, these treatments also inhibited degranulation as well as PGD(2) and CysLT production through IgE-dependent activation of the mast cell lineage RBL-2H3. Conclusion: Curine significantly inhibited immediate allergic reactions through mechanisms more related to mast cell stabilization and activation inhibition than interference with the pro-inflammatory effects of mast cell products. These findings are in line with the hypothesis that the alkaloid curine may be beneficial for the treatment of allergic disorders. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1118 / 1124
页数:7
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