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古古勒脂单独及与阿司匹林联合应用对大鼠大脑中动脉闭塞(MCAO)局灶性脑缺血模型的神经保护作用。

Neuroprotective effect of guggulipid alone and in combination with aspirin on middle cerebral artery occlusion (MCAO) model of focal cerebral ischemia in rats.

作者信息

Ahmad Mohd Afroz, Najmi Abul Kalam, Mujeeb Mohd, Akhtar Mohd

机构信息

Department of Pharmacology, Faculty of Pharmacy , Jamia Hamdard, New Delhi , India and.

出版信息

Toxicol Mech Methods. 2014 Sep;24(6):438-47. doi: 10.3109/15376516.2014.939320. Epub 2014 Jul 15.

DOI:10.3109/15376516.2014.939320
PMID:24965906
Abstract

This study was designed to test the pre-treatment doses of guggulipid (50 mg/kg), aspirin (100 mg/kg) per orally and co-administration of both drugs for 28 days followed by middle cerebral artery occlusion - a model of focal cerebral ischemia in rats. Middle cerebral artery was occluded for two hours, followed by reperfusion for 22 hours for the induction of focal cerebral ischemia in rats. Neurobehavioral tests like locomotor activity and grip strength tests were performed before sacrificing the animal. After neurobehavioral tests, the animals were sacrificed for the measurement of infarction areas and biochemical estimations in brain. Locomotor activity and grip strength were significantly improved in guggulipid and aspirin pre-treated rats. Guggulipid and aspirin pre-treatment reduced the infarction areas as compared with middle cerebral occluded (MCAO) rats. An elevation of nitrite, thiobarbituric acid reactive substance (TBARS), acetylcholine esterase activity (AchE) and reduction in antioxidant enzymes like superoxide dismutase (SOD), glutathione (GSH) and catalase were observed following MCAO. Pre-treatment with guggulipid and aspirin caused a reduction in TBARS and nitrite levels, AchE, but elevated GSH level, SOD and catalase activities as compared with MCAO rats. The protective effects observed in this study were due to antioxidant, anti-inflammatory and anti-hyperlipidemic properties of guggulipid. The protective effect of guggulipid in cerebral ischemia, that it may have a role in reversing the symptoms and may offer significant neuroprotection in stroke.

摘要

本研究旨在测试古古勒脂(50毫克/千克)、阿司匹林(100毫克/千克)的口服预处理剂量以及两种药物联合给药28天,随后进行大脑中动脉闭塞——一种大鼠局灶性脑缺血模型。大脑中动脉闭塞两小时,随后再灌注22小时以诱导大鼠局灶性脑缺血。在处死动物前进行了诸如运动活性和握力测试等神经行为学测试。神经行为学测试后,处死动物以测量梗死面积并进行脑内生化评估。古古勒脂和阿司匹林预处理的大鼠运动活性和握力显著改善。与大脑中动脉闭塞(MCAO)大鼠相比,古古勒脂和阿司匹林预处理减少了梗死面积。MCAO后观察到亚硝酸盐、硫代巴比妥酸反应性物质(TBARS)、乙酰胆碱酯酶活性(AchE)升高,以及超氧化物歧化酶(SOD)、谷胱甘肽(GSH)和过氧化氢酶等抗氧化酶减少。与MCAO大鼠相比,古古勒脂和阿司匹林预处理导致TBARS和亚硝酸盐水平、AchE降低,但GSH水平、SOD和过氧化氢酶活性升高。本研究中观察到的保护作用归因于古古勒脂的抗氧化、抗炎和抗高脂血症特性。古古勒脂在脑缺血中的保护作用表明,它可能在逆转症状方面发挥作用,并可能在中风中提供显著的神经保护。

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