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Intravenous Treatment with a Long-Chain Omega-3 Lipid Emulsion Provides Neuroprotection in a Murine Model of Ischemic Stroke – A Pilot Study

机译:用长链Omega-3脂质乳液进行静脉治疗可在鼠缺血性卒中模型中提供神经保护作用-一项初步研究

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摘要

Single long-chain omega-3 fatty acids (e.g. docosahexaenoic acid (DHA) or eicosapentaenoic acid (EPA)) are known for their neuroprotective properties associated with ischemic stroke. This pilot study aimed to test the effectiveness of an acute treatment with a long-chain omega-3 lipid emulsion (Omegaven 10%®, OGV) that contains fish oil (DHA 18 mg/ml; EPA 21 mg/ml) and α-tocopherol (0.2 mg/ml) in a transient middle cerebral artery occlusion (MCAO) model of ischemic stroke in mice. For this purpose, female CD-1 mice were anesthetized and subjected to 90 minutes of MCAO. To reflect a clinically relevant situation for an acute treatment, either after induction of stroke or after reperfusion, a single dose of OGV was injected intravenously into the tail vein (5 ml/kg b.w.). A neurological severity score was used to assess motor function and neurological outcome. Stroke-related parameters were determined 24 hours after MCAO. Microdialysis was used to collect samples from extracellular space of the striatum. Mitochondrial function was determined in isolated mitochondria or dissociated brain cells. Inflammation markers were measured in brain homogenate. According to control experiments, neuroprotective effects could be attributed to the long-chain omega-3 content of the emulsion. Intravenous injection of OGV reduced size and severity of stroke, restored mitochondrial function, and prevented excitotoxic glutamate release. Increases of pro-inflammatory markers (COX-2 and IL-6) were attenuated. Neurological severity scoring and neurochemical data demonstrated that acute OGV treatment shortly after induction of stroke was most efficient and able to improve short-term neurological outcome, reflecting the importance of an acute treatment to improve the outcome. Summarising, acute treatment of stroke with a single intravenous dose of OGV provided strong neuroprotective effects and was most effective when given immediately after onset of ischemia. As OGV is an approved fishoil emulsion for parenteral nutrition in humans, our results may provide first translational data for a possible early management of ischemic stroke with administration of OGV to prevent further brain damage.
机译:已知长链omega-3脂肪酸(例如二十二碳六烯酸(DHA)或二十碳五烯酸(EPA))具有与缺血性中风相关的神经保护特性。这项初步研究旨在测试含鱼油(DHA 18 mg / ml; EPA 21)的长链omega-3脂质乳液(Omegaven 10%®,OGV)急性治疗的有效性。毫克/毫升)和α-生育酚(0.2毫克/毫升)在小鼠缺血性中风的短暂脑中动脉闭塞(MCAO)模型中。为此,将雌性CD-1小鼠麻醉并进行90分钟的MCAO。为了反映急性中风后或再灌注后急性治疗的临床相关情况,将单剂量的OGV静脉注射到尾静脉中(5 ml / kg b.w.)。神经病学严重程度评分用于评估运动功能和神经学结局。在MCAO后24小时确定中风相关参数。微透析用于从纹状体的细胞外空间收集样品。在分离的线粒体或分离的脑细胞中测定线粒体功能。在脑匀浆中测量炎症标志物。根据对照实验,神经保护作用可归因于乳液中长链omega-3的含量。静脉注射OGV可减少中风的大小和严重程度,恢复线粒体功能,并防止兴奋性谷氨酸释放。促炎性标志物(COX-2和IL-6)的增加减弱。神经病学严重程度评分和神经化学数据表明,在诱发中风后不久进行急性OGV治疗最有效,能够改善短期神经系统预后,反映了急性治疗对改善预后的重要性。综上所述,单次静脉内注射OGV对中风的急性治疗提供了强大的神经保护作用,并且在缺血发作后立即给予最有效。由于OGV是批准用于人类肠胃外营养的鱼油乳剂,因此我们的研究结果可能会提供首个翻译数据,以指导早期应用OGV预防缺血性卒中,以防止进一步的脑损伤。

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