首页> 美国卫生研究院文献>Journal of Medicinal Food >Valeriana officinalis Extracts Ameliorate Neuronal Damage by Suppressing Lipid Peroxidation in the Gerbil Hippocampus Following Transient Cerebral Ischemia
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Valeriana officinalis Extracts Ameliorate Neuronal Damage by Suppressing Lipid Peroxidation in the Gerbil Hippocampus Following Transient Cerebral Ischemia

机译:缬草提取物通过抑制短暂性脑缺血后沙鼠海马中的脂质过氧化来改善神经元损伤。

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摘要

As a medicinal plant, the roots of Valeriana officinalis have been used as a sedative and tranquilizer. In the present study, we evaluated the neuroprotective effects of valerian root extracts (VE) on the hippocampal CA1 region of gerbils after 5 min of transient cerebral ischemia. Gerbils were administered VE orally once a day for 3 weeks, subjected to ischemia/reperfusion injury, and continued on VE for 3 weeks. The administration of 100 mg/kg VE (VE100 group) significantly reduced the ischemia-induced spontaneous motor hyperactivity 1 day after ischemia/reperfusion. Four days after ischemia/reperfusion, animals treated with VE showed abundant cresyl violet-positive neurons in the hippocampal CA1 region when compared to the vehicle or 25 mg/kg VE-treated groups. In addition, the VE treatment markedly decreased microglial activation in the hippocampal CA1 region 4 days after ischemia. Compared to the other groups, the VE100 group showed the lowest level of lipid peroxidation during the first 24 h after ischemia/reperfusion. In summary, the findings in this study suggest that pretreatment with VE has protective effects against ischemic injury in the hippocampal pyramidal neurons by decreasing microglial activation and lipid peroxidation.
机译:作为药用植物,缬草的根已被用作镇静剂和镇定剂。在本研究中,我们评估了缬草根提取物(VE)对短暂性脑缺血5分钟后沙土鼠海马CA1区的神经保护作用。每天一次给沙鼠口服VE,持续3周,遭受缺血/再灌注损伤,并持续VE 3周。给予100μmg/ kg V​​E(VE100组)可显着降低缺血/再灌注1天后缺血引起的自发性运动亢进。缺血/再灌注后四天,与媒介物或25μmg/ kg V​​E治疗组相比,用VE治疗的动物在海马CA1区显示出丰富的甲酚紫罗兰阳性神经元。另外,VE治疗在缺血后4天显着降低了海马CA1区的小胶质细胞活化。与其他组相比,VE100组在缺血/再灌注后的前24h内脂质过氧化水平最低。总之,这项研究的结果表明,VE预处理通过减少小胶质细胞激活和脂质过氧化作用,对海马锥体神经元缺血性损伤具有保护作用。

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