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首页> 外文期刊>Brain research >Sodium Ferulate combined with bone marrow stromal cell treatment ameliorating rat brain ischemic injury after stroke.
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Sodium Ferulate combined with bone marrow stromal cell treatment ameliorating rat brain ischemic injury after stroke.

机译:阿魏酸钠联合骨髓基质细胞治疗可改善中风后大鼠脑缺血性损伤。

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Reports suggested that bone marrow stromal cells (BMSCs) could protect brain against ischemic injury. However, the limited number of BMSCs in the brain hampered their application. To explore a way that might improve the migration and differentiation of BMSCs in the brain after stroke, we investigated the additive therapeutic effect of combination Sodium Ferulate (SF) and BMSCs treatment of stroke. In general, BMSCs were primarily cultured from rat bone marrow and were identified by flow cytometry. Permanent middle cerebral artery occlusion (MCAo) was induced and the ischemic brain was observed by 2,3,5-triphenyltetrazolium chloride (TTC) staining. The neurological functional outcome was respectively evaluated at 0 hour, 24 hours, 48 hours, and 72 hours post-operation, and the stromal cell-derived factor-1 alpha (SDF-1α) /chemokine(CXC motif)receptor-4(CXCR4) mRNA and protein expressions at the marginal zone of the ischemic brain were respectively measured by real-time RT-PCR and Western Blot at 3days after stroke; furthermore, Nestin and BrdU double immunostaining was performed for identification of BMSC differentiation. Combination treatment of Stroke significantly improved the neurological functional recovery as early as 48 hours and up-regulated the SDF-1α /CXCR4 axis, enhanced BMSC migration into the ischemic brain and differentiation into Nestin-positive cells. We demonstrate that SF combined with BMSC administration can ameliorate rat brain ischemic injury and has beneficial effect on the rat neurological functional recovery after ischemic stroke.
机译:报告表明,骨髓基质细胞(BMSC)可以保护大脑免受缺血性损伤。但是,大脑中有限数量的BMSC阻碍了它们的应用。为了探索可能改善脑卒中后脑干细胞迁移和分化的方法,我们研究了联合阿魏酸钠(SF)和脑干细胞治疗脑卒中的累加治疗效果。通常,BMSCs主要从大鼠骨髓中培养,并通过流式细胞仪进行鉴定。诱导永久性大脑中动脉闭塞(MCAo),并通过2,3,5-三苯四唑氯化物(TTC)染色观察缺血性脑。分别在术后0小时,24小时,48小时和72小时评估神经功能预后,并评估基质细胞衍生因子1α(SDF-1α)/趋化因子(CXC基序)受体4(CXCR4)中风后第3天,通过实时RT-PCR和Western Blot分别测定缺血性脑边缘区域的mRNA和蛋白质表达。此外,进行了Nestin和BrdU双重免疫染色以鉴定BMSC的分化。中风的联合治疗可在48小时内显着改善神经功能恢复,并上调SDF-1α/ CXCR4轴,增强BMSC向缺血性脑的迁移并向Nestin阳性细胞分化。我们证明SF结合BMSC给药可以减轻大鼠脑缺血性损伤,并且对缺血性中风后大鼠神经功能的恢复具有有益的作用。

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