Targeting adenosine receptors: novel therapeutic targets in asthma and chronic obstructive pulmonary disease.

Steuart Rorke, Stephen T Holgate
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引用次数: 25

Abstract

Adenosine, an endogenous signaling nucleoside that modulates many physiological processes has been implicated in playing an ever increasingly important role in the pathogenesis of asthma and chronic obstructive pulmonary disease (COPD). All cells contain adenosine and adenine nucleotides and the cellular production of adenosine is greatly enhanced under conditions of local hypoxia as may occur in inflammatory conditions such as asthma and COPD. In 1983, it was first reported that inhaled adenosine causes dose-related bronchoconstriction in patients with both allergic and non-allergic asthma but not in healthy volunteers. This hyperresponsiveness was also reported in patients with COPD, with those patients who smoked exhibiting a significantly greater response. This bronchoconstrictor effect of adenosine is orchestrated through the stimulation of specific cell membrane receptors and involves an important inflammatory cell, the mast cell. There is substantial evidence which suggests that mast cell activation is central to this unique response to adenosine. Mast cell mediator release makes a significant contribution towards airflow obstruction and the consequent symptoms in patients with asthma. Over the last two decades, researchers have investigated the effect of mast cell inhibitors as well as mast cell mediator receptor antagonists and their role in attenuating the bronchoconstrictor response to inhaled adenosine 5'-monophosphate (AMP). Promising results have been shown using mast cell stabilizers, histamine H1 receptor antagonists, selective cysteinyl leukotriene-1 receptor antagonists and inhibitors of 5-lipoxygenase and cyclo-oxygenase. Through these findings, the mast cell has been recognized as being a critical inflammatory cell in the adenosine-induced response in patients with asthma and COPD. To date, four subtypes (A1, A2A, A2B, A3) of adenosine receptors have been cloned each with a unique pattern of tissue distribution and signal transduction. Activation of these receptors has pro- and anti-inflammatory consequences making the development of agonists and/or antagonists at these receptor sites a novel approach in the treatment of patients with asthma and COPD. This review highlights the importance of adenosine in the pathophysiology of asthma and COPD, the critical role of the mast cell and the potential to target the adenosine receptor subtype in patients with asthma and COPD. The complete characterization of these adenosine receptor subtypes in terms of their distribution in humans and the development of selective agonists and antagonists, holds the key to our complete understanding of the role of this important mediator in asthma and COPD.

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靶向腺苷受体:哮喘和慢性阻塞性肺疾病的新治疗靶点。
腺苷是一种内源性信号核苷,可以调节许多生理过程,在哮喘和慢性阻塞性肺疾病(COPD)的发病机制中起着越来越重要的作用。所有细胞都含有腺苷和腺嘌呤核苷酸,在局部缺氧的情况下,腺苷的细胞生成大大增强,这可能发生在哮喘和慢性阻塞性肺病等炎症性疾病中。1983年,首次报道了吸入腺苷在过敏性和非过敏性哮喘患者中引起剂量相关的支气管收缩,但在健康志愿者中没有。这种高反应性在COPD患者中也有报道,吸烟的患者表现出明显更大的反应。腺苷的这种支气管收缩作用是通过刺激特定的细胞膜受体来协调的,并涉及一个重要的炎症细胞,肥大细胞。有大量证据表明,肥大细胞的活化是这种对腺苷的独特反应的核心。肥大细胞介质释放对哮喘患者气流阻塞和随之而来的症状有重要作用。在过去的二十年里,研究人员已经研究了肥大细胞抑制剂和肥大细胞介质受体拮抗剂的作用,以及它们在减轻吸入腺苷5'-单磷酸腺苷(AMP)对支气管收缩的反应中的作用。肥大细胞稳定剂、组胺H1受体拮抗剂、选择性半胱氨酸-白三烯-1受体拮抗剂以及5-脂氧合酶和环氧合酶抑制剂已显示出令人满意的结果。通过这些发现,肥大细胞被认为是哮喘和COPD患者中腺苷诱导反应的关键炎症细胞。迄今为止,已经克隆出四种腺苷受体亚型(A1, A2A, A2B, A3),每种亚型都具有独特的组织分布和信号转导模式。这些受体的激活具有促炎和抗炎作用,使得在这些受体位点开发激动剂和/或拮抗剂成为治疗哮喘和慢性阻塞性肺病患者的新方法。这篇综述强调了腺苷在哮喘和COPD的病理生理中的重要性,肥大细胞的关键作用以及在哮喘和COPD患者中靶向腺苷受体亚型的潜力。这些腺苷受体亚型在人类中的分布和选择性激动剂和拮抗剂的发展的完整表征,是我们完全理解这一重要介质在哮喘和COPD中的作用的关键。
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