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青蒿琥酯抗疟药在实验性肥大细胞介导的过敏性模型中的抗过敏作用。

Anti-allergic action of anti-malarial drug artesunate in experimental mast cell-mediated anaphylactic models.

机构信息

Department of Pharmacology, Yong Loo Lin School of Medicine, National University Health System, Singapore City, Singapore.

出版信息

Allergy. 2013 Feb;68(2):195-203. doi: 10.1111/all.12077. Epub 2012 Dec 18.

DOI:10.1111/all.12077
PMID:23253152
Abstract

BACKGROUND

Allergy is an acquired hypersensitivity reaction of the immune system mediated by cross-linking of allergen-specific IgE-bound high-affinity IgE receptors, leading to immediate mast cell degranulation. Artesunate is a semi-synthetic derivative of artemisinin, an active component of the medicinal plant Artemisia annua. Artesunate is a clinically effective anti-malarial drug and has recently been shown to attenuate allergic asthma in mouse models. This study investigated potential anti-allergic effects of artesunate in animal models of IgE-dependent anaphylaxis.

METHODS

Anti-allergic actions of artesunate were evaluated in passive cutaneous anaphylaxis and passive systemic anaphylaxis mouse models, and in ovalbumin-induced contraction of bronchial rings isolated from sensitized guinea pigs. Direct mast cell-stabilizing effect of artesunate was examined in RBL-2H3 mast cell line and in mature human cultured mast cells. Anti-allergic signaling mechanisms of action of artesunate in mast cells were also investigated.

RESULTS

Artesunate prevented IgE-mediated cutaneous vascular hyperpermeability, hypothermia, elevation in plasma histamine level, and tracheal tissue mast cell degranulation in mice in a dose-dependent manner. In addition, artesunate suppressed ovalbumin-mediated guinea pig bronchial smooth muscle contraction. Furthermore, artesunate concentration-dependently blocked IgE-mediated degranulation of RBL-2H3 mast cells and human culture mast cells. Artesunate was found to inhibit IgE-induced Syk and PLCγ1 phosphorylation, production of IP(3) , and rise in cytosolic Ca(+2) level in mast cells.

CONCLUSIONS

We report here for the first time that artesunate possesses anti-allergic activity by blocking IgE-induced mast cell degranulation, providing a foundation for developing artesunate for the treatment of allergic asthma and other mast cell-mediated allergic disorders.

摘要

背景

过敏是一种由过敏原特异性 IgE 结合的高亲和力 IgE 受体交联介导的获得性超敏反应,导致即刻肥大细胞脱颗粒。青蒿琥酯是青蒿素的半合成衍生物,青蒿素是药用植物黄花蒿的一种活性成分。青蒿琥酯是一种临床有效的抗疟药物,最近已被证明可减轻小鼠哮喘模型中的过敏反应。本研究探讨了青蒿琥酯在 IgE 依赖性过敏反应动物模型中的潜在抗过敏作用。

方法

在被动皮肤过敏和被动全身过敏小鼠模型中以及在卵白蛋白诱导的致敏豚鼠支气管环收缩中评估青蒿琥酯的抗过敏作用。在 RBL-2H3 肥大细胞系和成熟的人培养肥大细胞中检测青蒿琥酯对肥大细胞的直接稳定作用。还研究了青蒿琥酯在肥大细胞中的抗过敏信号作用机制。

结果

青蒿琥酯以剂量依赖性方式预防 IgE 介导的皮肤血管通透性增加、体温降低、血浆组胺水平升高和气管组织肥大细胞脱颗粒。此外,青蒿琥酯抑制卵白蛋白介导的豚鼠支气管平滑肌收缩。此外,青蒿琥酯浓度依赖性地阻断 IgE 介导的 RBL-2H3 肥大细胞和人培养肥大细胞的脱颗粒。发现青蒿琥酯抑制 IgE 诱导的 Syk 和 PLCγ1 磷酸化、IP(3) 的产生和细胞内 Ca(+2) 水平的升高。

结论

我们首次报道青蒿琥酯通过阻断 IgE 诱导的肥大细胞脱颗粒具有抗过敏活性,为开发青蒿琥酯治疗过敏哮喘和其他肥大细胞介导的过敏疾病提供了基础。

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