Department of Pharmaceutical Chemistry and Drug Analysis, Centre for Neuroscience, Vrije Universiteit Brussel, Laarbeeklaan 103, 1090 Brussels, Belgium.
Neurochem Int. 2013 Nov;63(5):379-88. doi: 10.1016/j.neuint.2013.07.011. Epub 2013 Aug 6.
Mild hypothermia is a promising neuroprotective therapy in stroke management. However, little is known about its effects on the global protein expression patterns in brain regions affected by ischemic stroke. We investigated protein expression changes associated with the neuroprotective effects of hypothermia via a functional proteomics approach through the analysis of the core (striatum) and the penumbra (cortex) after an ischemic insult in rats induced by endothelin-1 (Et-1). Functional outcome, infarct volume and related global protein expression changes were assessed 24h after the insult using two-dimensional difference gel electrophoresis. Mild hypothermia, induced 20 min after endothelin-1 infusion, improved the neurological outcome, reflected by a 36% reduction in infarct volume and a significantly better neurological deficit score. Hypothermia was typically associated with opposite protein expression changes inthe cortex to those induced by stroke under normothermic conditions, but not in the striatum. The main cellular processes rescued by hypothermia and potentially involved in the protection of the cortex are cellular assembly and organization, followed by cell signaling, thereby confirming that hypothermia is neuroprotective through multiple molecular and cellular pathways.
轻度低温是一种有前途的脑卒中管理神经保护疗法。然而,对于其对缺血性脑卒中影响的脑区的整体蛋白质表达模式的影响知之甚少。我们通过对内皮素-1(Et-1)诱导的大鼠缺血后核心(纹状体)和半影区(皮质)的功能蛋白质组学分析,研究了低温的神经保护作用相关的蛋白质表达变化。在损伤后 24 小时,使用二维差异凝胶电泳评估功能结果、梗死体积和相关的整体蛋白质表达变化。在内皮素-1输注 20 分钟后诱导轻度低温,可改善神经功能结局,表现为梗死体积减少 36%,神经缺陷评分显著改善。低温通常与正常体温条件下诱导的皮质卒中引起的相反的蛋白质表达变化相关,但在纹状体中则没有。低温拯救的主要细胞过程并可能涉及皮质的保护作用是细胞组装和组织,其次是细胞信号转导,从而证实低温通过多种分子和细胞途径具有神经保护作用。