Université Joseph Fourier Grenoble 1, GREPI/AGIM CNRS-UJF FRE 3405 and Centre de Référence des Angioedèmes CREAK, CHU Grenoble POBox 217, F-38043 Grenoble, France.
Expert Opin Pharmacother. 2012 Oct;13(15):2233-47. doi: 10.1517/14656566.2012.723692. Epub 2012 Sep 13.
HOE-140/ Icatibant is a selective, competitive antagonist to bradykinin (BK) against its binding to the kinin B2 receptor. Substitution of five non-proteogeneic amino acid analogues makes icatibant resistant to degradation by metalloproteases of kinin catabolism. Icatibant has clinical applications in inflammatory and vascular leakage conditions caused by an acute (non-controlled) production of kinins and their accumulation at the endothelium B2 receptor. The clinical manifestation of vascular leakage, called angioedema (AE), is characterized by edematous attacks of subcutaneous and submucosal tissues, which can cause painful intestinal consequences, and life-threatening complications if affecting the larynx. Icatibant is registered for the treatment of acute attacks of the hereditary BK-mediated AE, i.e., AE due to C1 inhibitor deficiency.
This review discusses emerging knowledge on the kinin system: kinin pharmacological properties, biochemical characteristics of the contact phase and kinin catabolism proteases. It underlines the responsibility of the kinins in AE initiation and the potency of icatibant to inhibit AE formation by kinin-receptor interactions.
Icatibant antagonist properties protect BK-mediated AE patients against severe attacks, and could be developed for use in inflammatory conditions. More studies are required to confirm whether or not prolonged and frequent applications of icatibant could result in the impairment of the cardioprotective effect of BK.
HOE-140/依卡替班是一种选择性、竞争性缓激肽(BK)拮抗剂,可与缓激肽 B2 受体结合。通过取代 5 个非蛋白基因类似物,依卡替班可抵抗激肽代谢中金属蛋白酶的降解。依卡替班在由激肽急性(非控制)产生及其在内皮 B2 受体蓄积引起的炎症和血管渗漏情况下具有临床应用。血管渗漏的临床表现称为血管性水肿(AE),其特征是皮下和黏膜下组织的水肿性发作,可引起疼痛的肠道后果,如果影响喉部,还会引起危及生命的并发症。依卡替班已注册用于治疗遗传性 BK 介导的 AE 的急性发作,即由于 C1 抑制剂缺乏引起的 AE。
本文综述了激肽系统的新知识:激肽的药理学特性、接触相的生化特征和激肽代谢蛋白酶。它强调了激肽在 AE 发作中的作用以及依卡替班通过抑制激肽受体相互作用抑制 AE 形成的效力。
依卡替班的拮抗剂特性可保护 BK 介导的 AE 患者免受严重发作的影响,并可开发用于炎症性疾病。需要更多的研究来证实依卡替班的延长和频繁应用是否会导致 BK 的心脏保护作用受损。