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首页> 外文期刊>Translational stroke research >Neuroprotection Induced by Energy and Protein-Energy Undernutrition Is Phase-Dependent After Focal Cerebral Ischemia in Mice
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Neuroprotection Induced by Energy and Protein-Energy Undernutrition Is Phase-Dependent After Focal Cerebral Ischemia in Mice

机译:通过能量和蛋白质 - 能量造成的神经保护作用是相依赖于小鼠局灶性脑缺血后的相依赖性

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摘要

Malnutrition predisposes to poor stroke outcome. In animal models, undernutrition protected against ischemic injury in some, but not in other studies. In view of diverse stroke models and food restriction paradigms, the consequences of undernutrition are poorly understood. Herein, we exposed mice to energy-reduced and protein-energy-reduced diets for 7-30 days and subsequently induced intraluminal middle cerebral artery occlusion. Undernutrition phase dependently influenced ischemic injury. Short-lasting 7 days of protein-energy undernutrition, but not energy undernutrition, decreased post-ischemic brain leukocyte infiltration and microglial activation and reduced brain Il-1 beta mRNA, but did not protect against ischemic injury. Fourteen days of energy and protein-energy undernutrition, on the other hand, reduced ischemic injury despite absence of anti-inflammatory effects. Anti-oxidant genes (Sod-1, Sod-2, and Cat mRNAs) were regulated in the liver and, to a lesser extent, the ischemic brain, indicating an adapted, compensated stage. Conversely, 30 days of energy and protein-energy undernutrition caused progressive animal exhaustion associated with post-ischemic hypoperfusion, rise of metabolic markers (Sirt-1 and Glut-1 mRNAs, Sirt-1 protein) in the ischemic brain, and reregulation of pro- and anti-oxidant markers (now also Nox-4 and Gpx-3 mRNAs) in the liver. In the latter condition, no neuroprotection was noted. Our study suggests an adaptation of metabolic systems that provides neuroprotection in a circumscribed time window.
机译:营养不良易导致卒中预后不良。在动物模型中,营养不良在一些研究中对缺血性损伤有保护作用,但在其他研究中没有。鉴于不同的中风模型和食物限制范例,营养不良的后果尚不清楚。在此,我们将小鼠暴露于能量减少和蛋白质能量减少的饮食中7-30天,随后诱导大脑中动脉腔内闭塞。营养不良阶段依赖性地影响缺血性损伤。短暂持续7天的蛋白质-能量营养不良,但不是能量营养不良,可减少缺血后的脑白细胞浸润和小胶质细胞活化,降低脑Il-1βmRNA表达,但不能防止缺血性损伤。另一方面,14天的能量和蛋白质能量营养不足虽然没有抗炎作用,但可以减少缺血性损伤。抗氧化基因(Sod-1、Sod-2和Cat mRNA)在肝脏中受到调节,在较小程度上,在缺血的大脑中也受到调节,表明处于适应性代偿阶段。相反,30天的能量和蛋白质能量营养不良会导致动物进行性衰竭,与缺血后低灌注、缺血脑内代谢标志物(Sirt-1和Glut-1 mRNA、Sirt-1蛋白质)的升高,以及肝脏中促氧化和抗氧化标志物(现在也是Nox-4和Gpx-3 mRNA)的重新调节有关。在后一种情况下,没有发现神经保护作用。我们的研究表明,代谢系统的适应性在限定的时间窗内提供神经保护。

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