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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Protective effect of Etoricoxib against middle cerebral artery occlusion induced transient focal cerebral ischemia in rats.
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Protective effect of Etoricoxib against middle cerebral artery occlusion induced transient focal cerebral ischemia in rats.

机译:依托考昔对大鼠大脑中动脉阻塞所致短暂性局灶性脑缺血的保护作用。

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摘要

Stroke is the third leading cause of global death and disability. Cyclooxygenase-2 mRNA has been shown to be up-regulated after stroke and also the time window of its expression extends from 4 to 12 h. The objective of this study was to elucidate the protective effect of Etoricoxib (a selective Cyclooxygenase-2 inhibitor) against transient middle cerebral artery occlusion induced behavioral, biochemical and histological alterations. Transient ischemia reperfusion significantly caused behavioral (neurological deficits, decreased locomotor activity and rotarod performance), biochemical (increased lipid peroxidation and nitrite concentration, while decreased superoxide dismutase and catalase activity) and histological (increased infarct volume) changes. Etoricoxib (3 and 10 mg/kg, i.p.) significantly reversed the alterations caused by cerebral ischemia however, 1 mg/kg dose was not found effective in any of the parameters. Finally, we can conclude that Etoricoxib has beneficial effects against transient middle cerebral artery occlusion model in rats. The present study indicates that Etoricoxib may be considered as a potential candidate in the treatment of stroke, clinically.
机译:中风是全球死亡和残疾的第三大原因。已经显示中风后环氧合酶2 mRNA上调,并且其表达的时间窗从4到12 h延长。这项研究的目的是阐明Etoricoxib(一种选择性的环氧合酶2抑制剂)对短暂性大脑中动脉阻塞引起的行为,生化和组织学改变的保护作用。短暂性脑缺血再灌注显着引起行为(神经功能缺损,运动能力和旋转子程序性能降低),生化(脂质过氧化和亚硝酸盐浓度增加,而超氧化物歧化酶和过氧化氢酶活性降低)和组织学(梗死体积增加)变化。依托昔布(3和10 mg / kg,腹腔注射)明显逆转了由脑缺血引起的改变,但是,在任何参数中均未发现1 mg / kg剂量有效。最后,我们可以得出结论,依托考昔对大鼠短暂性中脑动脉阻塞模型具有有益作用。本研究表明,在临床上,依托考昔可能被视为潜在的中风候选药物。

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