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从芒果中分离得到的 1,2,3,4,6-五-O-没食子酰基-β-d-葡萄糖苷减轻大鼠短暂性全脑缺血/再灌注诱导的脑损伤。

Alleviation of transient global ischemia/reperfusion-induced brain injury in rats with 1,2,3,4,6-penta-O-galloyl-β-d-glucopyranose isolated from Mangifera indica.

机构信息

Department of Pharmacology, PES College of Pharmacy, Hanumanthanagar, Bangalore 560050, Karnataka, India.

出版信息

Eur J Pharmacol. 2013 Nov 15;720(1-3):286-93. doi: 10.1016/j.ejphar.2013.10.016. Epub 2013 Oct 22.

Abstract

Present study was undertaken to evaluate the protective effect of 1,2,3,4,6-penta-O-galloyl-β-d-glucopyranose (PGG) against transient global ischemia/reperfusion (I/R)-induced brain injury in rats. Sixty minutes of global ischemia, followed by 24h of reperfusion caused significant alterations in cognition and memory (p<0.01), significant deterioration of motor coordination, grip strength, and limb tone (P<0.01) associated with neurological deficit. In addition, significant decrease in catalase (P<0.01), and superoxide dismutase (SOD) (P<0.01) activities, increase in lipid peroxidation (P<0.01), depletion of reduced glutathione (GSH) (P<0.01), and increase in brain volume (P<0.01) was observed. Additionally, I/R insult has aggravated the cerebral infarct formation (P<0.01), and the histopathology of brain showed congestion of blood vessels, edema of brain parenchyma, leukocyte infiltration as signs of neuroinflammation, and necrosis of brain tissue. Interestingly, pre-treatment with quercetin (20mg/kg, i.p.), and PGG (5 and 10mg/kg, i.p.) for 7 days showed significant, and dose dependent protection against I/R-induced brain injury by alleviating all the behavioral, neurological, morphological, and histological changes induced by I/R. Besides, PGG is a well-known antioxidant, and its protective effect against I/R-induced brain injury is thought to be due to its potent antioxidant property.

摘要

本研究旨在评估 1,2,3,4,6-五-O-没食子酰基-β-d-葡萄糖(PGG)对大鼠短暂全脑缺血/再灌注(I/R)损伤的保护作用。60 分钟的全脑缺血,随后 24 小时的再灌注导致认知和记忆发生显著改变(p<0.01),运动协调、握力和肢体张力显著恶化(P<0.01),并伴有神经功能缺损。此外,还观察到过氧化氢酶(P<0.01)和超氧化物歧化酶(SOD)(P<0.01)活性显著降低,脂质过氧化(P<0.01)增加,还原型谷胱甘肽(GSH)耗竭(P<0.01),脑体积增加(P<0.01)。此外,I/R 损伤加重了脑梗死的形成(P<0.01),脑组织的组织病理学显示血管充血、脑实质水肿、白细胞浸润,作为神经炎症的迹象,以及脑组织坏死。有趣的是,预先用槲皮素(20mg/kg,腹腔注射)和 PGG(5 和 10mg/kg,腹腔注射)治疗 7 天,通过减轻 I/R 引起的所有行为、神经、形态和组织学变化,显著且呈剂量依赖性地保护 I/R 诱导的脑损伤。此外,PGG 是一种众所周知的抗氧化剂,其对 I/R 诱导的脑损伤的保护作用可能归因于其强大的抗氧化特性。

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