首页> 美国卫生研究院文献>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
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A Proline Derivative-Enriched Fraction from Sideroxylon obtusifolium Protects the Hippocampus from Intracerebroventricular Pilocarpine-Induced Injury Associated with Status Epilepticus in Mice

机译:Sideroxylon obtusifolium富含脯氨酸的衍生物可保护海马免遭脑癫痫性脑脊髓炎所致的癫痫持续状态所致的伤害

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摘要

The -methyl-(2S,4R)-trans-4-hydroxy- -proline-enriched fraction (NMP) from 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 , ) and NMP-treated groups (Pilo 300 µg/1 µL icv, followed by 100 or 200 mg/kg ). 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-甲基-(2S,4R)-反式-4-羟基-脯氨酸的富集馏分(NMP)在脑室内(icv)毛果芸香碱(Pilo)模型中作为神经保护剂进行了评估。为此,将雄性小鼠分为假手术(SO,媒介物),皮洛(300 µg / 1 µL icv,其次是媒介物)和NMP处理组(皮洛300 µg / 1 µL icv,然后是100或200毫克/公斤)。皮洛注射液治疗后一天开始治疗,持续15天。 NMP的作用通过表征Y迷宫和物体识别测试中认知功能的保持来评估。通过尼氏染色评估海马细胞的生存力。研究了其他损伤标志物—胶质纤维酸性蛋白(GFAP)和离子钙结合适配器分子1(Iba-1)的表达,分别使用免疫荧光和蛋白质印迹分析。我们还进行了分子对接实验,揭示了NMP与γ-氨基丁酸(GABA)转运蛋白1(GAT1)结合。还表征了海马中GAT1的表达。毛细血管炎引起海马认知障碍,细胞损伤,GFAP,Iba-1和GAT1表达增加。尤其是通过较高的NMP剂量可以防止这些改变。这些数据突出显示,NMP是保护海马的有前途的候选药物,如icv Pilo模型所示。

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