...
首页> 外文期刊>International Journal of Molecular Sciences >A Proline Derivative-Enriched Fraction from Sideroxylon obtusifolium Protects the Hippocampus from Intracerebroventricular Pilocarpine-Induced Injury Associated with Status Epilepticus in Mice
【24h】

A Proline Derivative-Enriched Fraction from Sideroxylon obtusifolium Protects the Hippocampus from Intracerebroventricular Pilocarpine-Induced Injury Associated with Status Epilepticus in Mice

机译:来自Sideroxylon oderusium的脯氨酸衍生物富集部分保护海马免受与小鼠身份癫痫患者相关的颅内鳞状藻胺诱导的损伤

获取原文
   

获取外文期刊封面封底 >>

       

摘要

The N -methyl-(2S,4R)-trans-4-hydroxy- l -proline-enriched fraction (NMP) from Sideroxylon obtusifolium was evaluated as a neuroprotective agent in the intracerebroventricular (icv) pilocarpine (Pilo) model. To this aim, male mice were subdivided into sham (SO, vehicle), Pilo (300 μg/1 μL icv, followed by the vehicle per os , po ) and NMP-treated groups (Pilo 300 μg/1 μL icv, followed by 100 or 200 mg/kg po ). The treatments started one day after the Pilo injection and continued for 15 days. The effects of NMP were assessed by characterizing the preservation of cognitive function in both the Y-maze and object recognition tests. The hippocampal cell viability was evaluated by Nissl staining. Additional markers of damage were studied—the glial fibrillary acidic protein (GFAP) and the ionized calcium-binding adaptor molecule 1 (Iba-1) expression using, respectively, immunofluorescence and western blot analyses. We also performed molecular docking experiments revealing that NMP binds to the γ-aminobutyric acid (GABA) transporter 1 (GAT1). GAT1 expression in the hippocampus was also characterized. Pilo induced cognitive deficits, cell damage, increased GFAP, Iba-1, and GAT1 expression in the hippocampus. These alterations were prevented, especially by the higher NMP dose. These data highlight NMP as a promising candidate for the protection of the hippocampus, as shown by the icv Pilo model.
机译:来自Sideroxylon脱胆的N-甲基 - (2S,4R)-Trans-4-羟基-1-脯氨酸富集的级分(NMP)被评价为颅内腔内(ICV)纤维素(PLO)模型中的神经保护剂。为此目的,雄性小鼠被细分为假(所以,车辆),pilo(300μg/1μlCV,然后是每对OS,PO)和NMP处理的基团(Pilo300μg/1μLCV)中的100或200 mg / kg po)。该治疗在Plo注射后一天开始,并持续15天。通过表征在Y迷宫和物体识别试验中的认知功能的保存来评估NMP的影响。通过NISSL染色评价海马细胞活力。研究了胶质纤维酸性蛋白(GFAP)和使用免疫荧光和Western印迹分析的胶质纤维酸性蛋白(GFAP)和电离钙结合衔接子1(IBA-1)表达的额外标记。我们还表现出分子对接实验,显示NMP与γ-氨基丁酸(GABA)转运蛋白1(GAT1)结合。 SIPAPAMPS中的GAT1表达也表征。 Plo诱导了海马中的认知缺陷,细胞损伤,GFAP,IBA-1和GAT1表达。预防这些改变,特别是通过较高的NMP剂量。这些数据突出显示NMP作为保护海马的有希望的候选者,如ICV Pilo模型所示。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号