醋萘醇对大鼠局灶性脑缺血的影响。

S Briyal, U Sharma, N R Jagannathan, Y K Gupta
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引用次数: 5

摘要

本研究探讨了醋酸乙醇对脑卒中大鼠大脑中动脉闭塞模型的影响。用水合氯醛(400 mg/kg / p)麻醉大鼠,短暂性中动脉闭塞2小时。各组分别按10、20、40 mg/kg i.p.给药。共注射4次醋酸醇,分别为MCA闭塞时、MCA闭塞后1 h、再灌注时和再灌注后30 min。在MCA闭塞24小时后进行神经功能缺损和运动性能测试(握力、足部故障、旋转杆性能、自发运动活动测试)。之后,处死大鼠,测定氧化应激标志物:丙二醛(MDA)、还原型谷胱甘肽(GSH)和超氧化物歧化酶(SOD)。另一组接受车辆治疗的受试者也进行平行实验。与mca闭塞大鼠相比,10 mg/kg剂量的Vineatrol既不能改善神经功能缺损,也不能降低MDA升高水平。然而,高剂量的醋醇(20和40 mg/kg)提供了显著的保护,如运动性能测试得分增加和MCA闭塞后观察到的MDA水平升高的显著衰减所示。GSH和SOD水平显著升高。结果表明,醋萘醇能减轻脑卒中大鼠MCA闭塞模型局灶性缺血引起的神经元损伤。
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Effect of vineatrol in focal cerebral ischemia in rats.

The present study was carried out to examine the effect of administration of vineatrol in the middle cerebral artery (MCA) occlusion model of stroke in rats. Rats were anesthetized using chloral hydrate (400 mg/kg i.p.) and subjected to 2 h of transient MCA occlusion. Vineatrol was administered at doses of 10, 20 and 40 mg/kg i.p. to different groups. In total, four injections of vineatrol were given, i.e., at the time of MCA occlusion, 1 h after MCA occlusion, at the time of reperfusion and 30 min after reperfusion. Neurological deficit and motor performance tests (grip, foot fault, rotarod performance, spontaneous locomotor activity tests) were carried out 24 h after MCA occlusion. Thereafter, the rats were sacrificed to estimate markers of oxidative stress: malondialdehyde (MDA), reduced glutathione (GSH) and superoxide dismutase (SOD). A vehicle-treated group was also run in parallel. Vineatrol at the dose of 10 mg/kg i.p. neither improved neurological deficits nor decreased the elevated level of MDA compared with vehicle-treated MCA-occluded rats. However, higher doses of vineatrol (20 and 40 mg/kg i.p.) afforded significant protection, as shown by the increase in scoring on motor performance tests and significant attenuation of the elevated MDA level observed after MCA occlusion. Levels of GSH and SOD were significantly increased. The results demonstrate that administration of vineatrol is able to reduce the neuronal damage caused by focal ischemia in the MCA occlusion model of stroke in rats.

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