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Chronic Treatment with Red Wine Polyphenol Compounds Mediates Neuroprotection in a Rat Model of Ischemic Cerebral Stroke

机译:红葡萄酒多酚化合物的慢性治疗介导缺血性脑卒中大鼠模型的神经保护作用

摘要

In this study, we investigated the in vivo effects of red wine polyphenol compounds (RWPC) in rats that were submitted to middle cerebral occlusion as an experimental model of stroke. Male Wistar rats were given RWPC [30 mg/(kg · d) dissolved in drinking water] or water for 1 wk before being subjected to transient middle cerebral artery occlusion followed by reperfusion. Sham-operated rats were subjected to transient occlusion in which the filament was not completely introduced. The release of amino acids and energy metabolites were monitored by intracerebral microdialysis. The volume of the ischemic lesion was assessed 24 h after reperfusion. Proteomic analysis of brain tissue was performed to study the effects of ischemia and RWPC on specific protein expression. Treatment with RWPC completely prevented the burst of excitatory amino acids that occurred in response to ischemia in untreated rats and significantly reduced brain infarct volumes. Rats chronically treated with RWPC, however, had lower basal concentrations of energy metabolites, including glucose and lactate in the brain parenchyma, compared with untreated rats. Chronic RWPC treatment significantly enhanced the residual cerebral blood flow during occlusion and reperfusion in rats subjected to transient occlusion compared with untreated rats. This effect resulted from arterial vasodilatation, as the internal diameters of several arteries were significantly enlarged after RWPC treatment. Proteomic studies revealed the modulation by RWPC of the expression of proteins involved in the maintenance of neuronal caliber and axon formation, in the protection against oxidative stress, and in energy metabolism. These findings provide an experimental basis for the beneficial effects of RWPC on the neurovascular unit during stroke.
机译:在这项研究中,我们调查了红酒多酚化合物(RWPC)在大鼠中脑闭塞作为中风实验模型时的体内作用。给雄性Wistar大鼠RWPC [溶于饮用水30 mg /(kg·d)]或水1 wk,然后进行短暂的大脑中动脉阻塞,然后再灌注。假手术大鼠经历短暂的闭塞,其中丝未完全插入。通过脑内微透析监测氨基酸和能量代谢物的释放。再灌注后24小时评估缺血性病变的体积。进行了脑组织的蛋白质组学分析,以研究缺血和RWPC对特定蛋白表达的影响。 RWPC的治疗完全防止了未经治疗的大鼠因缺血而引起的兴奋性氨基酸爆发,并显着减少了脑梗死体积。然而,与未治疗的大鼠相比,用RWPC长期治疗的大鼠的脑实质中能量代谢物的基础浓度较低,包括葡萄糖和乳酸。与未经治疗的大鼠相比,长期RWPC治疗显着增强了短暂性阻塞的大鼠在阻塞和再灌注过程中的残留脑血流量。这种效果是由于动脉血管舒张引起的,因为在进行RWPC治疗后,几条动脉的内径显着增大。蛋白质组学研究揭示了RWPC对参与维持神经元口径和轴突形成,抗氧化应激和能量代谢的蛋白质表达的调节。这些发现为RWPC对中风期间神经血管单位的有益作用提供了实验基础。

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