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H1抗组胺药对黏附分子的影响:长期治疗的一种可能理论依据。

Effects of H1 antihistamines on adhesion molecules: a possible rationale for long-term treatment.

作者信息

Ciprandi G, Passalacqua G, Canonica G W

机构信息

Allergy and Respiratory Diseases, Department of Internal Medicine, University of Genoa, Genoa, Italy.

出版信息

Clin Exp Allergy. 1999 Jul;29 Suppl 3:49-53.

Abstract

Our knowledge of the mechanisms underlying the allergic reaction has increased rapidly and has revealed a complex network of cells, mediators and cytokines. The intercellular adhesion system (and the ICAM-1 molecule in particular) appeared to play a pivotal role in the accumulation of inflammatory cells at the site of allergic reaction. The new antihistamines have been demonstrated to be capable of affecting several phenomena of the allergic inflammation, including mediator release, cellular activation and adhesion molecule expression. Taking into consideration the central role of adhesion molecules, the modulation of their expression may represent an important therapeutic target. The nasal and the conjunctival challenges represent two useful models for the in vivo study of the antiallergic activity of drugs, as they allow investigation of a wide variety of parameters: inflammatory infiltrate, ICAM-1 expression, concentration of soluble mediators.

摘要

我们对过敏反应潜在机制的认识迅速增加,揭示了一个由细胞、介质和细胞因子组成的复杂网络。细胞间粘附系统(尤其是ICAM-1分子)似乎在过敏反应部位炎症细胞的积聚中起关键作用。已证明新型抗组胺药能够影响过敏炎症的多种现象,包括介质释放、细胞活化和粘附分子表达。考虑到粘附分子的核心作用,对其表达的调节可能是一个重要的治疗靶点。鼻腔和结膜激发试验是药物体内抗过敏活性研究的两种有用模型,因为它们允许研究多种参数:炎症浸润、ICAM-1表达、可溶性介质浓度。

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