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葡萄籽提取物对脑缺血的神经保护作用:一种蛋白质组学方法。

Neuroprotective effect of grape seed extract on brain ischemia: a proteomic approach.

机构信息

Bioactive Substances Laboratory, Biotechnology Centre, TechnopolisBorj-Cedria, BP-901, 2050, Hammam-Lif, Tunis, Tunisia.

Plateforme Protéomique PISSARO, Institut de Recherche et d'Innovation Biomédicale, Normandie Université, Mont Saint Aignan, France.

出版信息

Metab Brain Dis. 2019 Jun;34(3):889-907. doi: 10.1007/s11011-019-00396-2. Epub 2019 Feb 22.

Abstract

Stroke is one of the leading causes of long-lasting disability in human and oxidative stress an important underlying cause. Molecular insights into pathophysiology of ischemic stroke are still obscure, and the present study investigated the protective effect of high dosage Grape Seed Extract (GSE 2.5 g/kg) on brain ischemia-reperfusion (I/R) injury using a proteomic approach. Ischemia was realized by occlusion of the common carotid arteries for 30 min followed by 1 h reperfusion on control or GSE pre-treated rats, and a label-free quantification followed by mass spectrometry analysis used to evaluate I/R induced alterations in protein abundance and metabolic pathways as well as the protection afforded by GSE. I/R-induced whole brain ionogram dyshomeostasis, ultrastructural alterations, as well as inflammation into hippocampal dentate gyrus area, which were evaluated using ICP-OES, transmission electron microscopy and immuno-histochemistry respectively. I/R altered the whole brain proteome abundance among which 108 proteins were significantly modified (35 up and 73 down-regulated proteins). Eighty-four proteins were protected upon GSE treatment among which 27 were up and 57 down-regulated proteins, suggesting a potent protective effect of GSE close to 78%of the disturbed proteome. Furthermore, GSE efficiently prevented the brain from I/R-induced ion dyshomeostasis, ultrastructural alterations, inflammatory biomarkers as CD56 or CD68 and calcium burst within the hippocampus. To conclude, a potent protective effect of GSE on brain ischemia is evidenced and clinical trials using high dosage GSE should be envisaged on people at high risk for stroke.

摘要

中风是导致人类长期残疾的主要原因之一,氧化应激是其重要的潜在原因。缺血性中风病理生理学的分子机制仍不清楚,本研究采用蛋白质组学方法研究了高剂量葡萄籽提取物(GSE 2.5 g/kg)对脑缺血再灌注(I/R)损伤的保护作用。通过夹闭颈总动脉 30 分钟,然后在对照组或 GSE 预处理大鼠中再灌注 1 小时来实现缺血,使用无标记定量和质谱分析来评估 I/R 诱导的蛋白质丰度和代谢途径的变化以及 GSE 提供的保护作用。使用 ICP-OES、透射电子显微镜和免疫组织化学分别评估 I/R 诱导的全脑离子图谱失衡、超微结构改变以及海马齿状回区的炎症。I/R 改变了全脑蛋白质组的丰度,其中 108 种蛋白质显著改变(35 种上调和 73 种下调蛋白质)。GSE 处理后保护了 84 种蛋白质,其中 27 种上调和 57 种下调蛋白质,表明 GSE 具有很强的保护作用,接近 78%的失调蛋白质。此外,GSE 有效地防止了脑 I/R 诱导的离子失衡、超微结构改变、炎症生物标志物(如 CD56 或 CD68)和海马内钙爆发。总之,GSE 对脑缺血具有很强的保护作用,应该考虑在高风险中风人群中使用高剂量 GSE 进行临床试验。

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