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首页> 外文期刊>Neurological Research: An Interdisciplinary Quarterly Journal >Resveratrol attenuates brain damage in permanent focal cerebral ischemia via activation of PI3K/Akt signaling pathway in rats
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Resveratrol attenuates brain damage in permanent focal cerebral ischemia via activation of PI3K/Akt signaling pathway in rats

机译:白藜芦醇通过在大鼠中激活PI3K / AKT信号通路的激活来衰减永久性焦脑缺血的脑损伤

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摘要

Objective: The aim of this study was to evaluate the potential molecular mechanism of resveratrol (RSV) that attenuates brain damage from focal cerebral ischemia. Methods and materials: To investigate whether phosphatidylinositol 3-kinase/Akt (PI3K/Akt) pathway was involved in RSV anti-inflammatory and neuroprotective properties. Middle cerebral artery occlusion (MCAO) animal model was used in this study. Adult male Sprague-Dawley (SD) rats underwent MCAO, and then received treatment with RSV or vehicle after the onset of ischemia. PI3K inhibitor LY294002 was injected intracerebroventricularly to inhibit the PI3K/Akt signaling pathway. Neurological deficit scores and cerebral water content were assessed 24 h after MCAO. The inflammatory factors interleukin (IL)-1 beta, tumor necrosis factor (TNF alpha), and cyclooxygenase-2 (COX2) mRNA level were examined by real-time PCR. The enzymatic activity of myeloperoxidase (MPO) was measured 24 h after MCAO. The protein expression of phospho-Akt and COX2 in ischemic brain were determined by western blot. Results: RSV significantly reduced neurological deficit scores, cerebral water content and the enzymatic activity of MPO, all of which were abolished by LY294002 administration. Real-time PCR showed that RSV significantly suppressed the upregulation of the inflammatory factors IL-1 beta, TNF alpha, COX2 mRNA levels. RSV significantly inhibited upregulated the protein expression of COX2 24 h after MCAO, which effect was abolished by LY294002 administration. Conclusion: RSV attenuated ischemic brain damage induced by cerebral artery occlusion mainly through PI3K/Akt signaling pathway.
机译:目的:本研究的目的是评估白藜芦醇(RSV)的潜在分子机制,可抑制局灶性脑缺血的脑损伤。方法和材料:研究磷脂酰肌醇3-激酶/ AKT(PI3K / AKT)途径是否参与RSV抗炎和神经保护性能。本研究使用中脑动脉闭塞(MCAO)动物模型。成年男性Sprague-Dawley(SD)大鼠接受MCAO,然后在缺血发作后接受RSV或载体的治疗。 PI3K抑制剂LY294002被注射颅内腔内以抑制PI3K / AKT信号通路。在MCAO后24小时评估神经缺陷分数和脑水含量。通过实时PCR检查炎症因子白细胞介素(IL)-1β,肿瘤坏死因子(TNFα)和环氧化酶-2(COX2)mRNA水平。 MCAO后24小时测量髓过氧化物酶(MPO)的酶活性。通过Western印迹测定缺血性脑中磷酸-AKT和COX2的蛋白质表达。结果:RSV显着降低神经缺陷分数,脑水含量和MPO的酶活性,所有这些都被Ly294002给药取消了。实时PCR显示RSV显着抑制了炎症因子IL-1β,TNFα,COX2 mRNA水平的上调。 RSV显着抑制了MCAO后COX2 24h 24小时的蛋白质表达,其效果由Ly294002给药。结论:脑动脉闭塞的RSV衰减缺血性脑损伤主要通过PI3K / AKT信号通路。

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