二甲胺四环素:一种旧药物的再利用,以提高急性缺血性卒中组织纤溶酶原激活剂的使用和安全性。

D. Hess, S. Fagan
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引用次数: 4

摘要

只有一种美国食品和药物管理局批准用于急性缺血性卒中的药物:组织纤溶酶原激活剂(tPA)。由于时间窗口短和对脑出血(ICH)的恐惧,tPA仍未得到充分利用。开发与tPA联合使用的药物以提高有利恢复的几率并降低脑出血的风险是非常有兴趣的。米诺环素是一种广谱抗生素,在临床前缺血性脑卒中模型中被发现是一种神经保护剂。二甲胺四环素抑制基质金属蛋白酶-9,这是与tPA使用相关的脑出血的生物标志物。二甲胺四环素也是一种抗炎剂和抑制聚(adp -核糖)聚合酶-1。米诺环素在迄今为止进行的临床试验中是安全且耐受性良好的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Repurposing an old drug to improve the use and safety of tissue plasminogen activator for acute ischemic stroke: minocycline.
There is only 1 US Food and Drug Administration-approved drug for acute ischemic stroke: tissue plasminogen activator (tPA). Due to a short time window and fear of intracerebral hemorrhage (ICH), tPA remains underutilized. There is great interest in developing combination drugs to use with tPA to improve the odds of a favorable recovery and to reduce the risk of ICH. Minocycline is a broad-spectrum antibiotic that has been found to be a neuroprotective agent in preclinical ischemic stroke models. Minocycline inhibits matrix metalloproteinase-9, a biomarker for ICH associated with tPA use. Minocycline is also an anti-inflammatory agent and inhibits poly (ADP-ribose) polymerase-1. Minocycline has been safe and well tolerated in the clinical trials conducted to date.
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