首页> 外文期刊>International Journal of Molecular Sciences >Effect of Pretreatment with the NADPH Oxidase Inhibitor Apocynin on the Therapeutic Efficacy of Human Placenta-Derived Mesenchymal Stem Cells in Intracerebral Hemorrhage
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Effect of Pretreatment with the NADPH Oxidase Inhibitor Apocynin on the Therapeutic Efficacy of Human Placenta-Derived Mesenchymal Stem Cells in Intracerebral Hemorrhage

机译:NADPH氧化酶抑制剂Apocynin预处理对人胎盘来源的间充质干细胞治疗脑出血的疗效

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Several studies have demonstrated the beneficial effect of mesenchymal stem cells (MSCs) on intracerebral hemorrhage (ICH). Enhancement of the therapeutic efficacy of MSCs in ICH is necessary, considering the diseases high association with mortality and morbidity. Various preconditioning methods to enhance the beneficial properties of MSCs have been introduced. We suggested apocynin, a well-known nicotinamide adenine dinucleotide phosphate (NADPH) oxidase inhibitor, as a novel preconditioning regimen to enhance the therapeutic efficacy of MSCs in ICH. Rat ICH models were made using bacterial collagenase. 24 h after ICH induction, the rats were randomly divided into apocynin-preconditioned MSC-treated (Apo-MSC), na?ve MSC-treated and control groups. Hematoma volume, brain edema, and degenerating neuron count were compared at 48 h after the ICH induction. The expression of tight junction proteins (occludin, zona occludens [ZO]-1) were also compared. Hematoma size, hemispheric enlargement and degenerating neuron count were significantly lower in the Apo-MSC group than in the na?ve MSC group ( p = 0.004, 0.013 and 0.043, respectively), while the expression of occludin was higher ( p = 0.024). Apocynin treatment enhances the therapeutic efficacy of MSCs in ICH in the acute stage, through the improvement of the beneficial properties of MSCs, such as neuroprotection and the reinforcement of endovascular integrity of cerebral vasculature.
机译:几项研究证明了间充质干细胞(MSCs)对脑出血(ICH)的有益作用。考虑到与死亡率和发病率高度相关的疾病,有必要增强MSC在ICH中的治疗效果。已经介绍了各种增强MSC有益特性的预处理方法。我们提出了载脂蛋白,一种著名的烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶抑制剂,作为一种新型的预处理方案,可以增强MSC在ICH中的治疗效果。使用细菌胶原酶制备大鼠ICH模型。 ICH诱导后24 h,将大鼠随机分为载有Apocynin预处理的MSC处理组(Apo-MSC),纯MSC处理组和对照组。在ICH诱导后48 h比较血肿量,脑水肿和退化神经元计数。还比较了紧密连接蛋白(occludin,zona occludens [ZO] -1)的表达。 Apo-MSC组的血肿大小,半球增大和退化的神经元数量明显低于单纯MSC组(分别为p = 0.004、0.013和0.043),而occludin的表达较高(p = 0.024)。 。 Apocynin治疗通过改善MSC的有益特性(例如神经保护和增强脑血管的血管内完整性)来提高MSC在ICH急性期的治疗效果。

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