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Profile of intravenous glyburide for the prevention of cerebral edema following large hemispheric infarction: evidence to date

机译:格列本脲静脉预防大面积半球性脑梗死后脑水肿的概况:迄今为止的证据

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摘要

Glyburide (also known as glibenclamide) is a second-generation sulfonylurea drug that inhibits sulfonylurea receptor 1 (Sur1) at nanomolar concentrations. Long used to target KATP (Sur1–Kir6.2) channels for the treatment of diabetes mellitus type 2, glyburide was recently repurposed to target Sur1–transient receptor potential melastatin 4 (Trpm4) channels in acute central nervous system injury. Discovered nearly two decades ago, SUR1–TRPM4 has emerged as a critical target in stroke, specifically in large hemispheric infarction, which is characterized by edema formation and life-threatening brain swelling. Following ischemia, SUR1–TRPM4 channels are transcriptionally upregulated in all cells of the neurovascular unit, including neurons, astrocytes, microglia, oligodendrocytes and microvascular endothelial cells. Work by several independent laboratories has linked SUR1–TRPM4 to edema formation, with blockade by glyburide reducing brain swelling and death in preclinical models. Recent work showed that, following ischemia, SUR1–TRPM4 co-assembles with aquaporin-4 to mediate cellular swelling of astrocytes, which contributes to brain swelling. Additionally, recent work linked SUR1–TRPM4 to secretion of matrix metalloproteinase-9 (MMP-9) induced by recombinant tissue plasminogen activator in activated brain endothelial cells, with blockade of SUR1–TRPM4 by glyburide reducing MMP-9 and hemorrhagic transformation in preclinical models with recombinant tissue plasminogen activator. The recently completed GAMES (Glyburide Advantage in Malignant Edema and Stroke) clinical trials on patients with large hemispheric infarctions treated with intravenous glyburide (RP-1127) revealed promising findings with regard to brain swelling (midline shift), MMP-9, functional outcomes and mortality. Here, we review key elements of the basic science, preclinical experiments and clinical studies, both retrospective and prospective, on glyburide in focal cerebral ischemia and stroke.
机译:格列本脲(也称为格列苯脲)是第二代磺酰脲类药物,可在纳摩尔浓度下抑制磺酰脲类受体1(Sur1)。长期用于靶向KATP(Sur1-Kir6.2)通道来治疗2型糖尿病的人,格列本脲最近被重新用于靶向急性中枢神经系统损伤中的Sur1-瞬态受体电位褪黑素4(Trpm4)通道。在近二十年前发现的SUR1-TRPM4已成为中风的关键靶标,特别是在以水肿形成和威胁生命的脑肿胀为特征的大半球性脑梗塞中。缺血后,SUR1-TRPM4通道在神经血管单位的所有细胞(包括神经元,星形胶质细胞,小胶质细胞,少突胶质细胞和微血管内皮细胞)中转录上调。几个独立实验室的工作已将SUR1-TRPM4与水肿形成联系在一起,格列本脲可降低临床前模型中的脑肿胀和死亡。最近的研究表明,缺血后,SUR1-TRPM4与aquaporin-4共同组装,以介导星形胶质细胞的细胞膨胀,这有助于脑部膨胀。此外,最近的工作将SUR1-TRPM4与重组脑组织纤溶酶原激活物在活化的脑内皮细胞中诱导的基质金属蛋白酶9(MMP-9)的分泌联系在一起,并在临床前模型中通过格列本脲降低MMP-9和出血性转化来阻断SUR1-TRPM4。用重组组织纤溶酶原激活剂。最近完成的GAMES(格列本脲在恶性水肿和中风中的优势)在接受静脉内格列本脲(RP-1127)治疗的大半球性梗死患者中的临床试验显示,在脑肿胀(中线移位),MMP-9,功能预后和死亡。在这里,我们回顾了关于格列本脲在局灶性脑缺血和中风中的基础科学,临床前实验和临床研究的关键要素,包括回顾性和前瞻性。

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