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Granulocyte colony stimulating factor neuroprotective effects on spinal motoneurons after ventral root avulsion

机译:腹侧根部撕脱术后粒细胞集落刺激因子对脊髓运动神经元的神经保护作用

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G-CSF is a glycoprotein commonly used to treat neutropenia. Recent studies have shown that the G-CSF receptor (G-CSF-R) is expressed by neurons in the central nervous system (CNS), and neuroprotective effects of G-CSF have been observed. In this study, the influence of G-CSF treatment on the glial reactivity and synaptic plasticity of spinal motoneurons in rats subjected to ventral root avulsion (VRA) was investigated. Lewis rats (7 weeks old) were subjected to unilateral VRA and divided into two groups: G-CSF and placebo treated. The drug treated animals were injected subcutaneously with 200 μg/kg/day of G-CSF for 5 days post lesion. The placebo group received saline buffer. After 2 weeks, both groups were sacrificed and their lumbar intumescences processed for transmission electron microscopy (TEM), motoneuron counting, and immunohistochemistry with antibodies against GFAP, Iba-1, and synaptophysin. Furthermore, in vitro analysis was carried out, using newborn cortical derived astrocytes. The results indicated increased neuronal survival in the G-CSF treated group coupled with synaptic preservation. TEM analyses revealed an improved preservation of the synaptic covering in treated animals. Additionally, the drug treated group showed an increase in astroglial reactivity both in vivo and in vitro. The astrocytes also presented an increased cell proliferation rate when compared with the controls after 3 days of culturing. In conclusion, the present results suggest that G-CSF has an influence on the stability of presynaptic terminals in the spinal cord as well as on the astroglial reaction, indicating a possible neuroprotective action.
机译:G-CSF是一种通常用于治疗中性粒细胞减少症的糖蛋白。最近的研究表明,G-CSF受体(G-CSF-R)由中枢神经系统(CNS)中的神经元表达,并且已观察到G-CSF的神经保护作用。在这项研究中,研究了G-CSF处理对腹根部撕脱(VRA)大鼠的神经胶质反应性和脊髓运动神经元突触可塑性的影响。对Lewis大鼠(7周龄)进行单侧VRA治疗,分为两组:G-CSF和安慰剂治疗组。在病变后5天,皮下注射药物处理的动物200μg/ kg /天的G-CSF。安慰剂组接受生理盐水缓冲液。 2周后,将两组处死,并对其腰椎肿胀进行处理,以进行透射电子显微镜(TEM),运动神经元计数和抗GFAP,Iba-1和突触素的抗体的免疫组织化学。此外,使用新生的皮质衍生星形胶质细胞进行了体外分析。结果表明,G-CSF治疗组的神经元存活率提高,同时突触保留。 TEM分析显示,在治疗的动物中,突触覆盖物的保存得以改善。另外,药物治疗组在体内和体外均显示星形胶质反应性增加。与培养3天后的对照相比,星形胶质细胞还表现出增加的细胞增殖速率。总之,目前的结果表明,G-CSF对脊髓中突触前末端的稳定性以及星形胶质细胞反应有影响,表明可能存在神经保护作用。

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