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Nitrobenzylthioinosine mimics adenosine to attenuate the epileptiform discharge of hippocampal neurons from epileptic rats

机译:硝基苄基硫代肌氨酸模拟腺苷以减轻癫痫大鼠海马神经元的癫痫样放电

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摘要

Nitrobenzylthioinosine (NBTI), a specific inhibitor of type 1 equilibrative nucleoside transporter, could regulate the extracellular adenosine concentration and have protective roles in seizures. However, the protection mechanism of NBTI in seizures remains poorly understood. Here, the expression pattern and subcellular distribution of adenosine A1 receptor were detected by Western blot analysis and double-labeling immunofluorescence staining in Lithium Chloride-Pilocarpine induced epileptic rat model. At 24 h after pilocarpine induced rat seizures, hippocampal slices were prepared and the evoked excitatory postsynaptic currents (eEPSCs) amplitude of pyramidal neurons in hippocampus CA1 region was recorded using whole-cell patch clamp. In vivo, compared to control group, Western blotting analysis showed that the expression of adenosine A1 receptor protein was increased at 24 h and 72 h after seizure, didn't change at 0 min and 1 w, and decreased at 2 w. Double-label immunofluorescence revealed that adenosine A1 receptor was mainly expressed in the membrane and cytoplasm of neurons. In Vitro, adenosine decreased the eEPSCs amplitude of pyramidal neurons in hippocampus CA1 region, NBTI also had the same effect. Meantime, NBTI could further inhibit eEPSCs amplitude on the basis of lower concentration adenosine (50μM), and adenosine A1 receptor inhibitor DPCPX partially reversed this effect. Taken together, we confirmed that the expression of adenosine A1 receptor protein was increased in the early seizures and decreased in the late seizures. At the same time, NBTI mimics adenosine to attenuate the epileptiform discharge through adenosine A1 receptor, which might provide a novel therapeutic approach toward the control of epilepsy.
机译:硝基苄基硫代肌苷(NBTI)是1型平衡核苷转运蛋白的特异性抑制剂,可调节细胞外腺苷浓度并在癫痫发​​作中起保护作用。但是,NBTI在癫痫发作中的保护机制仍知之甚少。在这里,通过蛋白质印迹分析和双标记免疫荧光染色在氯化锂-毛果芸香碱诱发的癫痫大鼠模型中检测腺苷A1受体的表达模式和亚细胞分布。毛果芸香碱诱发大鼠癫痫发作后24小时,准备海马切片,并使用全细胞膜片钳记录海马CA1区锥体神经元的诱发兴奋性突触后突触电流(eEPSCs)幅度。在体内,与对照组相比,蛋白质印迹分析表明,癫痫发作后24 h和72 h,腺苷A1受体蛋白的表达增加,而在0 min和1 w时,腺苷A1受体蛋白的表达没有变化,而在2 w时,腺苷A1受体蛋白的表达下降。双标记免疫荧光显示腺苷A1受体主要在神经元的膜和细胞质中表达。体外,腺苷降低海马CA1区锥体神经元的eEPSCs振幅,NBTI也具有相同的作用。同时,NBTI可以在较低浓度的腺苷(50μM)的基础上进一步抑制eEPSCs的振幅,而腺苷A1受体抑制剂DPCPX则部分逆转了这种作用。两者合计,我们确认腺苷A1受体蛋白的表达在癫痫发作早期有所增加,而在癫痫发作晚期则减少。同时,NBTI模仿腺苷以减轻通过腺苷A1受体的癫痫样放电,这可能为控制癫痫病提供一种新颖的治疗方法。

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