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Intervention Effects of Ganoderma Lucidum Spores on Epileptiform Discharge Hippocampal Neurons and Expression of Neurotrophin-4 and N-Cadherin

机译:灵芝孢子对癫痫样放电海马神经元的干预作用及Neurotrophin-4和N-钙黏着蛋白的表达

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摘要

Epilepsy can cause cerebral transient dysfunctions. Ganoderma lucidum spores (GLS), a traditional Chinese medicinal herb, has shown some antiepileptic effects in our previous studies. This was the first study of the effects of GLS on cultured primary hippocampal neurons, treated with Mg2+ free medium. This in vitro model of epileptiform discharge hippocampal neurons allowed us to investigate the anti-epileptic effects and mechanism of GLS activity. Primary hippocampal neurons from <1 day old rats were cultured and their morphologies observed under fluorescence microscope. Neurons were confirmed by immunofluorescent staining of neuron specific enolase (NSE). Sterile method for GLS generation was investigated and serial dilutions of GLS were used to test the maximum non-toxic concentration of GLS on hippocampal neurons. The optimized concentration of GLS of 0.122 mg/ml was identified and used for subsequent analysis. Using the in vitro model, hippocampal neurons were divided into 4 groups for subsequent treatment i) control, ii) model (incubated with Mg2+ free medium for 3 hours), iii) GLS group I (incubated with Mg2+ free medium containing GLS for 3 hours and replaced with normal medium and incubated for 6 hours) and iv) GLS group II (neurons incubated with Mg2+ free medium for 3 hours then replaced with a normal medium containing GLS for 6 hours). Neurotrophin-4 and N-Cadherin protein expression were detected using Western blot. The results showed that the number of normal hippocampal neurons increased and the morphologies of hippocampal neurons were well preserved after GLS treatment. Furthermore, the expression of neurotrophin-4 was significantly increased while the expression of N-Cadherin was decreased in the GLS treated group compared with the model group. This data indicates that GLS may protect hippocampal neurons by promoting neurotrophin-4 expression and inhibiting N-Cadherin expression.
机译:癫痫病可导致大脑短暂性功能障碍。灵芝孢子(GLS)是一种传统的中草药,在我们以前的研究中显示出一些抗癫痫作用。这是GLS对无Mg 2 + 培养基处理的原代海马神经元影响的首次研究。这种癫痫样放电海马神经元的体外模型使我们能够研究GLS活性的抗癫痫作用和机制。培养<1日龄大鼠的原代海马神经元,并在荧光显微镜下观察其形态。通过神经元特异性烯醇化酶(NSE)的免疫荧光染色确认了神经元。研究了产生GLS的无菌方法,并使用连续稀释的GLS来测试海马神经元上GLS的最大无毒浓度。确定了GLS的最佳浓度为0.122 mg / ml,并用于后续分析。使用体外模型,将海马神经元分为四组,用于后续治疗:i)对照; ii)模型(与Mg 2 + 游离培养基孵育3小时); iii)GLS组I(孵育用含有GLS的不含Mg 2 + 的游离培养基培养3小时,然后替换为普通培养基并孵育6小时)和iv)GLS组II(不含Mg 2 + 的神经元孵育)培养基3个小时,然后换成含有GLS的普通培养基6个小时)。使用蛋白质印迹检测Neurotrophin-4和N-钙黏着蛋白的表达。结果表明,GLS处理后正常海马神经元数目增加,海马神经元形态得到很好的保留。此外,与模型组相比,GLS治疗组中神经营养蛋白-4的表达显着增加,而N-钙黏着蛋白的表达则降低。该数据表明,GLS可能通过促进Neurotrophin-4表达和抑制N-Cadherin表达来保护海马神经元。

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