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日本刺沙蚕(Iznka)纤溶酶可减少大鼠局灶性脑缺血模型的脑梗死、脑水肿,并增加抗氧化作用。

Neanthes japonica (Iznka) fibrinolytic enzyme reduced cerebral infarction, cerebral edema and increased antioxidation in rat models of focal cerebral ischemia.

机构信息

Department of Biochemistry and Molecular Biology, Norman Bethune College of Medicine, Jilin University, 126 Xinmin Street, Changchun, Jilin Province 130021, China.

出版信息

Neurosci Lett. 2011 Feb 1;489(1):16-9. doi: 10.1016/j.neulet.2010.11.057. Epub 2010 Dec 1.

DOI:10.1016/j.neulet.2010.11.057
PMID:21129442
Abstract

Thrombolytic agent is increasingly being used in treating acute ischemic stroke. A novel protease with strong thrombolytic activity, Neanthes japonica (Iznka) fibrinolytic enzyme (NJF) discovered in our laboratory has been reported with characteristics of direct hydrolyzing fibrin and fibrinogen. The neuroprotective effect of NJF and urokinase (UK) was tested in rat models of middle cerebral artery occlusion (MCAO). The model was successfully produced by introducing an intraluminal suture into the left middle cerebral artery (MCA). NJF (0.25, 0.5, 1mg/kg) was injected intravenously 1h after the onset of reperfusion. Compared with vehicle group, MCAO animals treated with NJF showed dose dependent reduction in cerebral infarction with improved neurological outcome. Meanwhile, ischemia induced cerebral edema was reduced in a dose dependent manner. Treatment with NJF at 0.5mg/kg was almost equivalent to UK at 15,000U/kg dosage in the reduction of cerebral infarction and cerebral edema. Biomedical assay showed that NJF treatment suppressed lipid peroxidation and restored superoxide dismutase (SOD) activities in brain tissue. These results suggest that NJF posses neuroprotective potential in rat MCAO and reperfusion model. Neuroprotection shown by NJF may be attributed to inhibition of lipid peroxidation, increase in endogenous antioxidant defense enzymes.

摘要

溶栓剂在治疗急性缺血性中风中的应用越来越多。我们实验室发现了一种新型的蛋白酶,日本伊氏涡虫(Iznka)纤维蛋白溶解酶(NJF),具有很强的溶栓活性,其特点是直接水解纤维蛋白和纤维蛋白原。NJF 和尿激酶(UK)的神经保护作用在大脑中动脉闭塞(MCAO)大鼠模型中进行了测试。该模型通过将腔内缝线插入左大脑中动脉(MCA)成功产生。再灌注后 1 小时,静脉注射 NJF(0.25、0.5、1mg/kg)。与载体组相比,NJF 治疗的 MCAO 动物表现出剂量依赖性的脑梗死减少和神经功能改善。同时,缺血诱导的脑水肿也呈剂量依赖性减少。NJF 治疗 0.5mg/kg 的效果与 UK 治疗 15000U/kg 的效果相当,可减少脑梗死和脑水肿。生物医学检测表明,NJF 治疗可抑制脂质过氧化反应,并恢复脑组织中超氧化物歧化酶(SOD)的活性。这些结果表明,NJF 在大鼠 MCAO 和再灌注模型中具有神经保护作用。NJF 显示的神经保护作用可能归因于抑制脂质过氧化反应,增加内源性抗氧化防御酶。

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