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A sphingosine‐1‐phosphate receptor type 1 agonist ASP4058 suppresses intracranial aneurysm through promoting endothelial integrity and blocking macrophage transmigration

机译:鞘氨醇-1-磷酸受体1型激动剂ASP4058通过促进内皮完整性和阻断巨噬细胞转运而抑制颅内动脉瘤

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摘要

Background and PurposeIntracranial aneurysm (IA), common in the general public, causes lethal subarachnoid haemorrhage on rupture. It is, therefore, of utmost importance to prevent the IA from rupturing. However, there is currently no medical treatment. Recent studies suggest that IA is the result of chronic inflammation in the arterial wall caused by endothelial dysfunction and infiltrating macrophages. The sphingosine‐1‐phosphate receptor type 1 (S1P1 receptor) is present on the endothelium and promotes its barrier function. Here we have tested the potential of an S1P1 agonist, ASP4058, to prevent IA in an animal model.
机译:背景与目的颅内动脉瘤(IA)在普通大众中很常见,会在破裂时引起致命的蛛网膜下腔出血。因此,至关重要的是防止IA破裂。但是,目前没有药物治疗。最近的研究表明,IA是由内皮功能障碍和巨噬细胞浸润引起的动脉壁慢性炎症的结果。 1型鞘氨醇-1-磷酸受体(S1P1受体)存在于内皮细胞中,并促进其屏障功能。在这里,我们测试了S1P1激动剂ASP4058在动物模型中预防IA的潜力。

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