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白藜芦醇可保护沙鼠免受全脑缺血性损伤。

Resveratrol protects against global cerebral ischemic injury in gerbils.

作者信息

Wang Qun, Xu Jianfeng, Rottinghaus George E, Simonyi Agnes, Lubahn Dennis, Sun Grace Y, Sun Albert Y

机构信息

Department of Pharmacology, School of Medicine, M526 Medical Science Bldg, 1 Hospital Drive, University of Missouri-Columbia, Columbia, MO 65212, USA.

出版信息

Brain Res. 2002 Dec 27;958(2):439-47. doi: 10.1016/s0006-8993(02)03543-6.

Abstract

Increased oxidative stress has been implicated in the mechanisms of delayed neuronal cell death (DND) following cerebral ischemic insult. In this study, we investigated whether resveratrol, a polyphenolic antioxidant enriched in grape, may ameliorate ischemia-induced neuron cell death. Mongolian gerbils were divided into three groups, namely, sham control, ischemia and ischemia treated with resveratrol. Transient global cerebral ischemia was induced by occlusion of both common carotid arteries (CCA) for 5 min. Resveratrol was injected i.p. (30 mg/kg body weight), either during or shortly after CCA occlusion, and again at 24 h after ischemia. Cerebral blood flow was monitored before and during CCA occlusion using a laser Doppler flowmeter. Brain sections were immuno-stained for neurons, astrocytes and microglial cells. A time course study was also carried out to assess the bioavailability of resveratrol in serum, liver and brain using high performance liquid chromatography (HPLC). Morphometric measurements indicated extensive DND in the hippocampal CA1 region 4 days after ischemia and that neuron cell death was marked by the increase in reactive astrocytes and microglial cells. Administration of resveratrol, either during or after CCA occlusion, significantly (P<0.05) decreased DND as well as glial cell activation. Analysis of resveratrol after i.p. injection indicated its presence in serum, liver and brain with peak activity at 1, 4 and 4 h, respectively. This study demonstrated for the first time that resveratrol, a polyphenolic antioxidant, can cross the blood-brain barrier and exert protective effects against cerebral ischemic injury.

摘要

氧化应激增加与脑缺血损伤后迟发性神经元细胞死亡(DND)的机制有关。在本研究中,我们调查了葡萄中富含的多酚类抗氧化剂白藜芦醇是否可以改善缺血诱导的神经元细胞死亡。将蒙古沙鼠分为三组,即假手术对照组、缺血组和白藜芦醇治疗的缺血组。通过双侧颈总动脉(CCA)闭塞5分钟诱导短暂性全脑缺血。在CCA闭塞期间或闭塞后不久腹腔注射白藜芦醇(30mg/kg体重),并在缺血后24小时再次注射。使用激光多普勒血流仪在CCA闭塞前后监测脑血流量。脑切片对神经元、星形胶质细胞和小胶质细胞进行免疫染色。还使用高效液相色谱法(HPLC)进行了一项时间进程研究,以评估白藜芦醇在血清、肝脏和大脑中的生物利用度。形态学测量表明,缺血后4天海马CA1区存在广泛的DND,神经元细胞死亡以反应性星形胶质细胞和小胶质细胞增加为特征。在CCA闭塞期间或之后给予白藜芦醇可显著(P<0.05)减少DND以及胶质细胞活化。腹腔注射后对白藜芦醇的分析表明其存在于血清、肝脏和大脑中,活性峰值分别在1、4和4小时出现。本研究首次证明,多酚类抗氧化剂白藜芦醇可以穿过血脑屏障并对脑缺血损伤发挥保护作用。

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