靶向ONOO-/HMGB1/MMP-9信号级联:中药药物开发减轻缺血性脑损伤和溶栓治疗引起的出血转化的潜力

Hansen Chen, Binghe Guan, Jiangang Shen
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引用次数: 8

摘要

中风是世界范围内导致死亡和残疾的主要原因,缺血性中风占中风发病率的85%以上。组织纤溶酶原激活剂(Tissue plasminogen activator, t-PA)是fda唯一批准的用于缺血性卒中治疗的药物,治疗时间窗较窄,仅为4.5小时。出血转化(Hemorrhagic transformation, HT)是延迟t-PA治疗缺血性卒中的严重并发症。因此,开发联合疗法以减少HT和延长t-PA的治疗时间窗至关重要。目前的进展表明,过氧亚硝酸盐(ONOO-)/高迁移率组盒1蛋白(HMGB1)/基质金属蛋白酶-9 (MMP-9)信号级联可能对急性缺血性卒中溶栓治疗期间减轻HT很重要。近年来,从中药中寻找减轻缺血性脑卒中损伤的天然化合物取得了重要进展,其中一些靶向ONOO-/HMGB1/MMP-9信号级联。在此,我们分析了这三个靶点在介导HT中的作用和相互作用;随后,我们总结了中草药中可能具有减毒作用的化合物,并分析了相关靶点。最后,我们提出了在进一步开发这些化合物作为联合治疗中需要解决的潜在问题。
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Targeting ONOO-/HMGB1/MMP-9 Signaling Cascades: Potential for Drug Development from Chinese Medicine to Attenuate Ischemic Brain Injury and Hemorrhagic Transformation Induced by Thrombolytic Treatment
Stroke is the leading cause of death and disability worldwide, and ischemic stroke accounts for more than 85% of the stroke incidence. Tissue plasminogen activator (t-PA) is the only FDA-approved drug for ischemic stroke treatment with a narrow treatment time window of 4.5 h. Hemorrhagic transformation (HT) is a severe complication of delayed t-PA treatment in ischemic stroke. Thus, it is critically important to develop combination therapies to reduce HT and extend the therapeutic time window of t-PA. Current progress suggests that peroxynitrite (ONOO-)/high-mobility group box 1 protein (HMGB1)/matrix metalloproteinase-9 (MMP-9) signaling cascades could be important for attenuating HT during thrombolytic treatment for acute ischemic stroke. Recently, important progress has been made in seeking for natural compounds from Chinese medicine for reducing ischemic stroke injury, with some of them targeting ONOO-/HMGB1/MMP-9 signaling cascades. Herein, we analyze the roles and interactions of these three targets in mediating HT; subsequently, we summarize the potential compounds from Chinese herbal medicine for attenuating HT and analyze the related targets. Finally, we raise the potential issues to be addressed in further development of these compounds as combination therapy.
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