Curine inhibits mast cell-dependent responses in mice
被引:19
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作者:
Ribeiro-Filho, Jaime
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Fiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, BrazilFiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, Brazil
Ribeiro-Filho, Jaime
[1
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Leite, Fagner Carvalho
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机构:
Univ Fed Paraiba, Dept Fisiol & Patol, Lab Imunofarmacol, Joao Pessoa, Paraiba, BrazilFiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, Brazil
Leite, Fagner Carvalho
[4
]
Costa, Hermann Ferreira
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机构:
Univ Fed Paraiba, Dept Fisiol & Patol, Lab Imunofarmacol, Joao Pessoa, Paraiba, BrazilFiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, Brazil
Costa, Hermann Ferreira
[4
]
Calheiros, Andrea Surrage
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Fiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, BrazilFiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, Brazil
Calheiros, Andrea Surrage
[1
]
Torres, Rafael Carvalho
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机构:
Fiocruz MS, Inst Oswaldo Cruz, Lab Inflamacao, BR-21045900 Rio De Janeiro, BrazilFiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, Brazil
Torres, Rafael Carvalho
[2
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de Azevedo, Carolina Trindade
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机构:
Fiocruz MS, Inst Oswaldo Cruz, Lab Inflamacao, BR-21045900 Rio De Janeiro, BrazilFiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, Brazil
de Azevedo, Carolina Trindade
[2
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Martins, Marco Aurelio
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机构:
Fiocruz MS, Inst Oswaldo Cruz, Lab Inflamacao, BR-21045900 Rio De Janeiro, BrazilFiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, Brazil
Martins, Marco Aurelio
[2
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Dias, Celidarque da Silva
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机构:
Univ Fed Paraiba, Dept Ciencias Farmaceut, Lab Fitoquim, Joao Pessoa, Paraiba, BrazilFiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, Brazil
Dias, Celidarque da Silva
[3
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Bozza, Patricia T.
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Fiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, BrazilFiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, Brazil
Bozza, Patricia T.
[1
]
Piuvezam, Marcia Regina
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Univ Fed Paraiba, Dept Fisiol & Patol, Lab Imunofarmacol, Joao Pessoa, Paraiba, BrazilFiocruz MS, Inst Oswaldo Cruz, Lab Imunofarmacol, BR-21040360 Rio De Janeiro, RJ, Brazil
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
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.
机构:
Tufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Tufts Med Ctr, Boston, MA USATufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Kempuraj, D.
Tagen, M.
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机构:
Tufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Tufts Med Ctr, Boston, MA USATufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Tagen, M.
Iliopoulou, B. P.
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机构:
Tufts Med Ctr, Boston, MA USA
Tufts Univ, Sch Med, Dept Pathol, Boston, MA 02111 USATufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Iliopoulou, B. P.
Clemons, A.
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机构:
Tufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Tufts Med Ctr, Boston, MA USATufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Clemons, A.
Vasiadi, M.
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机构:
Tufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Tufts Med Ctr, Boston, MA USATufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Vasiadi, M.
Boucher, W.
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机构:
Tufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Tufts Med Ctr, Boston, MA USATufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Boucher, W.
House, M.
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机构:
Tufts Med Ctr, Boston, MA USA
Tufts Univ, Sch Med, Dept Obstet & Gynecol, Boston, MA 02111 USATufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
House, M.
Wolfberg, A.
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机构:
Tufts Med Ctr, Boston, MA USA
Tufts Univ, Sch Med, Dept Obstet & Gynecol, Boston, MA 02111 USATufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Wolfberg, A.
Theoharides, T. C.
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机构:
Tufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
Tufts Med Ctr, Boston, MA USA
Tufts Univ, Sch Med, Dept Internal Med, Boston, MA 02111 USA
Tufts Univ, Sch Med, Dept Biochem, Boston, MA 02111 USATufts Univ, Sch Med, Lab Mol Immunopharmacol & Drug Discovery, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA