Department of Pharmaceutical and Administrative Sciences, Loma Linda University School of Pharmacy, Loma Linda, CA 92350, USA.
Department of Psychology, University of California, San Diego, CA 92093, USA.
Int J Mol Sci. 2017 Dec 19;18(12):2756. doi: 10.3390/ijms18122756.
Tissue plasminogen activator (tPA) thrombolysis remains the gold standard treatment for ischemic stroke. A time-constrained therapeutic window, with the drug to be given within 4.5 h after stroke onset, and lethal side effects associated with delayed treatment, most notably hemorrhagic transformation (HT), limit the clinical use of tPA. Co-administering tPA with other agents, including drug or non-drug interventions, has been proposed as a practical strategy to address the limitations of tPA. Here, we discuss the pharmacological and non-drug approaches that were examined to mitigate the complications-especially HT-associated with delayed tPA treatment. The pharmacological treatments include those that preserve the blood-brain barrier (e.g., atovarstatin, batimastat, candesartan, cilostazol, fasudil, minocycline, etc.), enhance vascularization and protect the cerebrovasculature (e.g., coumarin derivate IMM-H004 and granulocyte-colony stimulating factor (G-CSF)), and exert their effects through other modes of action (e.g., oxygen transporters, ascorbic acid, etc.). The non-drug approaches include stem cell treatments and gas therapy with multi-pronged biological effects. Co-administering tPA with the abovementioned therapies showed promise in attenuating delayed tPA-induced side effects and stroke-induced neurological and behavioral deficits. Thus, adjunctive treatment approach is an innovative therapeutic modality that can address the limitations of tPA treatment and potentially expand the time window for ischemic stroke therapy.
组织型纤溶酶原激活物(tPA)溶栓仍然是缺血性脑卒中的金标准治疗方法。由于存在时间限制的治疗窗口,药物必须在脑卒中发作后 4.5 小时内给予,并且与延迟治疗相关的致命副作用,尤其是出血性转化(HT),限制了 tPA 的临床应用。与 tPA 联合使用其他药物或非药物干预措施,已被提议作为解决 tPA 治疗局限性的实用策略。在这里,我们讨论了为减轻与延迟 tPA 治疗相关的并发症(尤其是 HT)而检查的药理学和非药物方法。药理学治疗包括那些可保护血脑屏障的方法(例如阿托伐他汀、巴曲酶、坎地沙坦、西洛他唑、法舒地尔、米诺环素等)、增强血管生成和保护脑血管的方法(例如香豆素衍生物 IMM-H004 和粒细胞集落刺激因子(G-CSF)),以及通过其他作用模式发挥作用的方法(例如氧载体、抗坏血酸等)。非药物方法包括干细胞治疗和具有多种生物学效应的气体治疗。tPA 与上述疗法联合应用在减轻延迟 tPA 诱导的副作用和脑卒中引起的神经和行为缺陷方面显示出了前景。因此,辅助治疗方法是一种创新的治疗模式,可以解决 tPA 治疗的局限性,并有可能扩大缺血性脑卒中治疗的时间窗。