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喹唑啉类 Otaplimastat(SP-8203)可减少延迟 rtPA 诱导的溶栓后缺血性脑卒中的出血性转化和死亡率加重。

The Quinazoline Otaplimastat (SP-8203) Reduces the Hemorrhagic Transformation and Mortality Aggravated after Delayed rtPA-Induced Thrombolysis in Cerebral Ischemia.

机构信息

Department of Neuroscience, Korea University College of Medicine, Seoul 02841, Korea.

Research Headquarters, Shin Poong Pharm. Co., Ltd., Ansan 15610, Korea.

出版信息

Int J Mol Sci. 2022 Jan 26;23(3):1403. doi: 10.3390/ijms23031403.

Abstract

Acute ischemic stroke is the leading cause of morbidity and mortality worldwide. Recombinant tissue plasminogen activator (rtPA) is the only agent clinically approved by FDA for patients with acute ischemic stroke. However, delayed treatment of rtPA (e.g., more than 3 h after stroke onset) exacerbates ischemic brain damage by causing intracerebral hemorrhage and increasing neurotoxicity. In the present study, we investigated whether the neuroprotant otaplimastat reduced delayed rtPA treatment-evoked neurotoxicity in male Sprague Dawley rats subjected to embolic middle cerebral artery occlusion (eMCAO). Otaplimastat reduced cerebral infarct size and edema and improved neurobehavioral deficits. In particular, otaplimastat markedly reduced intracerebral hemorrhagic transformation and mortality triggered by delayed rtPA treatment, consequently extending the therapeutic time window of rtPA. We further found that ischemia-evoked extracellular matrix metalloproteases (MMPs) expression was closely correlated with cerebral hemorrhagic transformation and brain damage. In ischemic conditions, delayed rtPA treatment further increased brain injury via synergistic expression of MMPs in vascular endothelial cells. In oxygen-glucose-deprived endothelial cells, otaplimastat suppressed the activity rather than protein expression of MMPs by restoring the level of tissue inhibitor of metalloproteinase (TIMP) suppressed in ischemia, and consequently reduced vascular permeation. This paper shows that otaplimastat under clinical trials is a new drug which can inhibit stroke on its own and extend the therapeutic time window of rtPA, especially when administered in combination with rtPA.

摘要

急性缺血性脑卒中是全球发病率和死亡率的主要原因。重组组织型纤溶酶原激活剂(rtPA)是 FDA 唯一批准用于急性缺血性脑卒中患者的药物。然而,rtPA 的延迟治疗(例如,发病后超过 3 小时)会通过引起脑出血和增加神经毒性而加剧缺血性脑损伤。在本研究中,我们研究了神经保护剂奥塔普利马司特是否可以减少雄性 Sprague Dawley 大鼠栓塞性大脑中动脉闭塞(eMCAO)后接受延迟 rtPA 治疗引起的神经毒性。奥塔普利马司特可减少脑梗死面积和水肿,并改善神经行为缺陷。特别是,奥塔普利马司特明显减少了延迟 rtPA 治疗引起的脑出血转化和死亡率,从而延长了 rtPA 的治疗时间窗。我们进一步发现,缺血诱导的细胞外基质金属蛋白酶(MMPs)表达与脑出血转化和脑损伤密切相关。在缺血条件下,延迟的 rtPA 治疗通过协同表达血管内皮细胞中的 MMPs 进一步增加了脑损伤。在缺氧葡萄糖剥夺的内皮细胞中,奥塔普利马司特通过恢复缺血抑制的组织金属蛋白酶抑制剂(TIMP)水平来抑制 MMPs 的活性而不是蛋白表达,从而减少血管通透性。本文表明,正在临床试验中的奥塔普利马司特是一种新药,它可以单独抑制中风,并延长 rtPA 的治疗时间窗,尤其是与 rtPA 联合使用时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/136b/8835804/994ef5b3a53c/ijms-23-01403-g001.jpg

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