1 Institut National de la Santé et de la Recherche Médicale (INSERM), U1078 Brest, France.
2 Faculté de médecine et des Sciences de la Santé, Université de Bretagne Occidentale (UBO), Brest, France.
J Cereb Blood Flow Metab. 2018 Jun;38(6):1070-1084. doi: 10.1177/0271678X17712163. Epub 2017 Jun 1.
Stroke is a devastating disorder that significantly contributes to death, disability and healthcare costs. In ischemic stroke, the only current acute therapy is recanalization, but the narrow therapeutic window less than 6 h limits its application. The current challenge is to prevent late cell death, with concomitant therapy targeting the ischemic cascade to widen the therapeutic window. Among potential neuroprotective drugs, cyclin-dependent kinase inhibitors such as (S)-roscovitine are of particular relevance. We previously showed that (S)-roscovitine crossed the blood-brain barrier and was neuroprotective in a dose-dependent manner in two models of middle cerebral artery occlusion (MCAo). According to the Stroke Therapy Academic Industry Roundtable guidelines, the pharmacokinetics of (S)-roscovitine and the optimal mode of delivery and therapeutic dose in rats were investigated. Combination of intravenous (IV) and continuous sub-cutaneous (SC) infusion led to early and sustained delivery of (S)-roscovitine. Furthermore, in a randomized blind study on a transient MCAo rat model, we showed that this mode of delivery reduced both infarct and edema volume and was beneficial to neurological outcome. Within the framework of preclinical studies for stroke therapy development, we here provide data to improve translation of pre-clinical studies into successful clinical human trials.
中风是一种破坏性疾病,会导致死亡、残疾和医疗保健费用增加。在缺血性中风中,唯一的急性治疗方法是再通,但治疗窗口狭窄(小于 6 小时)限制了其应用。当前的挑战是预防迟发性细胞死亡,同时针对缺血级联反应进行伴随治疗以扩大治疗窗口。在潜在的神经保护药物中,细胞周期蛋白依赖性激酶抑制剂如(S)-罗斯考维汀(roscovitine)具有特别重要的意义。我们之前的研究表明,(S)-罗斯考维汀能够穿过血脑屏障,并在两种大脑中动脉阻塞(MCAo)模型中以剂量依赖性方式发挥神经保护作用。根据卒中治疗学术工业圆桌会议指南,研究了(S)-罗斯考维汀的药代动力学以及在大鼠中的最佳给药方式和治疗剂量。静脉(IV)和连续皮下(SC)输注的联合使用可实现(S)-罗斯考维汀的早期和持续递送。此外,在短暂性 MCAo 大鼠模型的随机盲法研究中,我们表明这种给药方式可减少梗死和水肿体积,对神经功能预后有益。在中风治疗开发的临床前研究框架内,我们在此提供了数据,以提高临床前研究向成功的临床人体试验的转化。