Medway School of Pharmacy, University of Kent, Chatham Maritime, United Kingdom.
Front Biosci (Landmark Ed). 2012 Jan 1;17(2):430-7. doi: 10.2741/3936.
It has long been recognised that mast cells and basophils are prominent sources of preformed histamine in humans and that this biogenic amine serves as one of the most important inflammatory mediators. In allergic diseases, histamine has previously been shown to partially modulate symptoms such as airway obstruction, mucus secretion, reddening of the skin and itch, all of which were attributed to engagement of H₁-receptors with the amine. However, more recently it has been shown that certain key biological functions of histamine, such as itch, are also crucially controlled by H₄-receptor stimulation, resulting in a growing interest in combinational anti-H1 and -H₄ therapeutic approaches. Moreover, research is beginning to shed light on a role of H₄-receptors in mast cell precursor trafficking to various tissues commonly affected by allergic inflammation. Furthermore, H₄-receptors are also expressed on mature basophils and other effector cells of allergic reactions, such as eosinophils. This presents exciting possibilities in terms of potentially modulating the pro-allergic function of these cells as well as.
长期以来,人们一直认为肥大细胞和嗜碱性粒细胞是人类预先形成的组织胺的主要来源,而这种生物胺是最重要的炎症介质之一。在过敏性疾病中,组织胺先前被证明可以部分调节气道阻塞、黏液分泌、皮肤发红和瘙痒等症状,所有这些都归因于与胺结合的 H₁-受体。然而,最近的研究表明,组织胺的某些关键生物学功能,如瘙痒,也受到 H₄-受体刺激的关键控制,这导致人们对组合抗 H1 和 -H₄ 治疗方法的兴趣日益浓厚。此外,研究开始揭示 H₄-受体在肥大细胞前体向各种受过敏炎症影响的常见组织中的迁移中的作用。此外,H₄-受体也表达在成熟的嗜碱性粒细胞和过敏反应的其他效应细胞,如嗜酸性粒细胞上。这为调节这些细胞的过敏功能以及其他功能提供了令人兴奋的可能性。