Mapracorat, a novel non-steroidal selective glucocorticoid receptor agonist for the treatment of allergic conjunctivitis.

Monica Baiula, Santi Spampinato
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引用次数: 24

Abstract

Glucocorticoids are used to treat chronic and severe forms of allergic conjunctivitis. Although they exert a rapid and powerful therapeutic activity, relevant side effects may limit their ocular use: increase of intraocular pressure, cataract formation and reduced resistance to infections. New glucocorticoids displaying the same potency of classical glucocorticoids but with fewer adverse effects are needed for the treatment of ocular disorders. Mapracorat (also known as ZK245186 or BOL-303242-X) is a novel non-steroidal selective glucocorticoid receptor agonist that is in the first phases of clinical evaluation (Phase II Clinical trials) for topical treatment of inflammatory skin and ocular disorders. Mapracorat binds selectively to human glucocorticoid receptor and displays powerful anti-inflammatory effects. In experimental models of ocular diseases, mapracorat reduces clinical symptoms, eosinophil recruitment, chemokines and pro-inflammatory cytokines production at ocular level, confirming that it acts preventing both the early and late phase of allergic response. Interestingly, mapracorat induces a lower increase of intraocular pressure in comparison to the classical glucocorticoid dexamethasone. Several clinical trials are ongoing to investigate the efficacy and safety of mapracorat for the treatment of several ocular diseases. Transrepressive mechanisms are thought to account for the majority of mapracorat's antiinflammatory effects; however, the induction of anti-inflammatory proteins likely involved in transactivation events may contribute to mapracorat-mediated anti-inflammatory properties and deserve to be further investigated in suitable in vivo and in vitro models. These observations may influence how novel "differential" ligands are discovered, identified and evaluated.

一种用于治疗过敏性结膜炎的新型非甾体选择性糖皮质激素受体激动剂。
糖皮质激素用于治疗慢性和严重形式的过敏性结膜炎。虽然它们具有快速和强大的治疗作用,但相关的副作用可能限制它们在眼部的使用:眼压升高、白内障形成和降低对感染的抵抗力。新型的糖皮质激素与传统的糖皮质激素具有相同的效力,但副作用更少,需要用于眼部疾病的治疗。Mapracorat(也被称为ZK245186或BOL-303242-X)是一种新型的非甾体选择性糖皮质激素受体激动剂,目前正处于临床评估的第一阶段(II期临床试验),用于局部治疗炎症性皮肤和眼部疾病。Mapracorat选择性结合人糖皮质激素受体,显示出强大的抗炎作用。在眼部疾病的实验模型中,mapracorat在眼部水平上减少临床症状、嗜酸性粒细胞募集、趋化因子和促炎细胞因子的产生,证实它可以预防过敏反应的早期和晚期。有趣的是,与经典的糖皮质激素地塞米松相比,mapracorat诱导的眼压升高较低。目前正在进行几项临床试验,以研究mapracorat治疗几种眼部疾病的有效性和安全性。反抑制机制被认为是mapracorat抗炎作用的主要原因;然而,抗炎蛋白的诱导可能参与了反活化事件,这可能有助于mapracort介导的抗炎特性,值得在合适的体内和体外模型中进一步研究。这些观察结果可能会影响如何发现、鉴定和评估新的“差异”配体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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