Effects of adenosine A2A receptor low affinity agonist Regadenoson in patients with obstructive pulmonary disease, at risk for adenosine-induced bronchoconstriction mediated via A2B and/or A3 adenosine receptors.

Stefan H. Meyering, H. Lomas
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Abstract

The pharmaceutical Regadenoson (Lexiscan TM ) Produced by Astellas Inc. Is currently in use as a pharmacological stress agent for myocardial perfusion imaging within the field of Nuclear Cardiology. Regadenoson is a selective A 2A adenosine receptor agonist, and also has a low affinity for adenosine receptors which cause bronchoconstriction in patients with reactive airways mediated via A 2B and A3 adenosine receptors. In a study of 42 patients with mild to moderate asthma and/or moderate to severe COPD who had a positive adenosine monophosphate test, Regadenoson proved to be relatively safe and well tolerated by most patients (90%). 8 Regadenoson is a low affinity agonist (Ki "H 1.3 µM) for the A2A adenosine receptor, with at least 10-fold lower affinity for the A1 adenosine receptor (Ki > 16.5 µM), and weak, if any, affinity for the A2B and A3 adenosine receptors. 2,9 Activation of the A2A adenosine receptor by regadenoson produces coronary vasodilation 8 and increases coronary blood flow (CBF). It
腺苷A2A受体低亲和力激动剂Regadenoson在A2B和/或A3腺苷受体介导的有腺苷诱导支气管收缩风险的阻塞性肺疾病患者中的作用
药物Regadenoson (Lexiscan TM)由安斯泰来公司生产。目前在核心脏病学领域被用作心肌灌注成像的药理学应激剂。Regadenoson是一种选择性的a2a腺苷受体激动剂,对通过a2b和A3腺苷受体介导的反应性气道患者引起支气管收缩的腺苷受体也具有低亲和力。在一项42例轻至中度哮喘和/或中至重度COPD患者的研究中,大多数患者(90%)的单磷酸腺苷试验阳性,Regadenoson被证明是相对安全且耐受性良好的。Regadenoson是A2A腺苷受体的低亲和力激动剂(Ki ' H 1.3µM),对A1腺苷受体的亲和力至少低10倍(Ki > 16.5µM),对A2B和A3腺苷受体的亲和力较弱(如果有的话)。regadenoson激活A2A腺苷受体可产生冠状动脉血管舒张8并增加冠状动脉血流量(CBF)。它
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