Department of Biochemistry, The Stroke Program, Yong Loo Lin School of Medicine, National University Health System, National University of Singapore, 8 Medical Drive, Singapore, 117597, Singapore.
Transl Stroke Res. 2010 Dec;1(4):287-303. doi: 10.1007/s12975-010-0035-3.
Pathogenesis of cerebral ischemia has so far been described in the context of proteins and the pathways that they regulate. The discovery of biomarkers has also been focussed mainly on proteins and to some extent on the mRNAs that encode them. The knowledge on the role of microRNAs in understanding the pathogenesis of cerebral ischemia is still at its infancy. In this study, using rat models subjected to middle cerebral artery occlusion, we have profiled the microRNAs at different reperfusion times (0 to 48 h) to understand the progression of cerebral ischemia. We have also attempted to correlate the expression of microRNAs to treatment with an NMDA antagonist (MK801) and to protein expression with the hope of demonstrating the potential use of microRNAs as early biomarkers of stroke.
迄今为止,脑缺血的发病机制是在蛋白质及其调节途径的背景下描述的。生物标志物的发现也主要集中在蛋白质上,在某种程度上也集中在编码它们的 mRNAs 上。关于 microRNAs 在理解脑缺血发病机制中的作用的知识仍处于起步阶段。在这项研究中,我们使用大脑中动脉闭塞的大鼠模型,在不同再灌注时间(0 至 48 小时)对 microRNAs 进行了分析,以了解脑缺血的进展。我们还试图将 microRNAs 的表达与 NMDA 拮抗剂(MK801)的治疗相关联,并将 microRNAs 的表达与蛋白质表达相关联,希望证明 microRNAs 作为中风早期生物标志物的潜在用途。