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首页> 外文期刊>Stroke: A Journal of Cerebral Circulation >Protecting against cerebrovascular injury: contributions of 12/15-lipoxygenase to edema formation after transient focal ischemia.
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Protecting against cerebrovascular injury: contributions of 12/15-lipoxygenase to edema formation after transient focal ischemia.

机译:预防脑血管损伤:短暂性局灶性局部缺血后12 / 15-脂氧合酶对水肿形成的作用。

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摘要

BACKGROUND AND PURPOSE: The concept of the neurovascular unit suggests that effects on brain vasculature must be considered if neuroprotection is to be achieved in stroke. We previously reported that 12/15-lipoxygenase (12/15-LOX) is upregulated in the peri-infarct area after middle cerebral artery occlusion in mice, and 12/15-LOX contributes to brain damage after ischemia-reperfusion. The current study was designed to investigate 12/15-LOX involvement in vascular injury in the ischemic brain. METHODS: In cell culture, a human brain microvascular endothelial cell line was subjected to either hypoxia or H(2)O(2)-induced oxidative stress with or without lipoxygenase inhibitors. For in vivo studies, mice were subjected to 90 minutes middle cerebral artery occlusion, and the effects of either 12/15-LOX gene knockout or treatment with lipoxygenase inhibitors were compared. Expression of 12/15-LOX and claudin-5 as well as extravasation of immunoglobulin G were detected by immunohistochemistry. Edema was measured as water content of brain hemispheres according to the wet-dry weight method. RESULTS: Brain endothelial cells were protected against hypoxia and H(2)O(2) by the lipoxygenase inhibitor baicalein. After focal ischemia, 12/15-LOX was increased in neurons and endothelial cells. The vascular tight junction protein claudin-5 underwent extensive degradation in the peri-infarct area, which was partially prevented by the lipoxygenase inhibitor baicalein. Leakage of immunoglobulin G into the brain parenchyma was significantly reduced in 12/15-LOX knockout mice as well as wild-type mice treated with baicalein. Likewise, brain edema was significantly ameliorated. CONCLUSIONS: 12/15-LOX may contribute to ischemic brain damage not just by causing neuronal cell death, but also by detrimental effects on the brain microvasculature. 12/15-LOX inhibitors may thus be effective as both neuroprotectants and vasculoprotectants.
机译:背景和目的:神经血管单位的概念表明,如果要在卒中中实现神经保护,必须考虑对脑血管的影响。我们先前曾报道过,小鼠中脑动脉闭塞后,梗死周围区域的12 / 15-脂氧合酶(12 / 15-LOX)上调,而12 / 15-LOX则导致缺血再灌注后脑损伤。当前的研究旨在调查12 / 15-LOX参与缺血性脑血管损伤。方法:在细胞培养中,使用或不使用脂氧合酶抑制剂对人脑微血管内皮细胞系进行缺氧或H(2)O(2)诱导的氧化应激。为了进行体内研究,将小鼠大脑中动脉闭塞90分钟,比较12 / 15-LOX基因敲除或脂氧合酶抑制剂治疗的效果。通过免疫组织化学检测12 / 15-LOX和claudin-5的表达以及免疫球蛋白G的外渗。根据湿干重法将水肿作为脑半球的水分含量进行测量。结果:脂氧合酶抑制剂黄ical素可保护脑内皮细胞免于缺氧和H(2)O(2)。局灶性缺血后,神经元和内皮细胞中12 / 15-LOX升高。血管紧密连接蛋白claudin-5在梗塞周围区域广泛降解,部分被脂氧合酶抑制剂黄ical素阻止。在12 / 15-LOX基因敲除小鼠以及用黄ical素治疗的野生型小鼠中,免疫球蛋白G向脑实质的泄漏显着减少。同样,脑水肿得到明显改善。结论:12 / 15-LOX可能不仅导致神经元细胞死亡,而且还通过对脑微血管的有害作用,导致缺血性脑损伤。因此,12 / 15-LOX抑制剂既可以作为神经保护剂也可以作为血管保护剂。

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