The role of glial glutamate transporter in the baseline synaptic response and short-term synaptic plasticity of CA1 area of the hippocampus in male Wistar rat

Negin Saeedi, S. Heysieattalab, M. Janahmadi, N. Hosseinmardi
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Abstract

Background. Glial cells release different gliotransmitters and response to neurotransmitters released from neurons. These cells especially astrocytes, having different transporters, play an important role in synaptic space homeostasis and synaptic plasticity. In this study, the role of hippocampal glial glutamate transporter (EAAT2) in baseline synaptic response and short term synaptic plasticity were investigated. Methods. In this experimental study, ceftriaxone, EAAT2 activator (0.5mmol/0.5μl), was microinjected intrahippcampally for activation of hippocampal glial glutamate transporter in male wistar rats. Baseline synaptic response and short term synaptic plasticity were evaluated by field potential recording. fEPSP was recorded from CA1 following Schaffer collaterals stimulation. After Input/Output curve construction, short term synaptic plasticity was induced by paired pulse stimulations. Results. Activation of EAAT2 by ceftriaxone microinjection in CA1 did not have any effect on baseline synaptic response (P> 0.05, Two Way ANOVA). There was no significant difference in Paired Pulse Index at 20, 80, and 200 ms inter-pulse interval between ceftriaxone treated and control group (P> 0.05, Two Way ANOVA). Conclusion. The results suggest that hippocampal glial glutamate transporter activation does not have effect on baseline synaptic response and short term synaptic plasticity in CA1 area of the hippocampus. Practical implications. Considering the role of glial cells in regulating the excitability of the nervous system as well as synaptic plasticity, correcting these features of the nervous system by manipulating glial cells can help the treatment or prevention of neurological diseases. In this study, the role of glial cells in the homeostasis of the glutamate in the synaptic space of the hippocampus was evaluated, through the stimulation of its uptake, on the basic synaptic activity and short-term synaptic plasticity.
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神经胶质谷氨酸转运体在雄性Wistar大鼠海马CA1区基线突触反应和短期突触可塑性中的作用
背景。神经胶质细胞释放不同的胶质递质,并对神经元释放的神经递质作出反应。这些细胞,尤其是星形胶质细胞,具有不同的转运体,在突触空间稳态和突触可塑性中起着重要作用。本研究探讨了海马胶质谷氨酸转运蛋白(EAAT2)在基线突触反应和短期突触可塑性中的作用。方法。本实验采用海马内注射EAAT2激活剂头孢曲松(0.5mmol/0.5μl),激活雄性wistar大鼠海马胶质谷氨酸转运体。通过场电位记录评价基线突触反应和短期突触可塑性。在沙弗络刺激后,从CA1记录fEPSP。构建输入/输出曲线后,采用配对脉冲刺激诱导短期突触可塑性。结果。头孢曲松微注射激活CA1区EAAT2对基线突触反应无影响(P> 0.05,双因素方差分析)。头孢曲松治疗组与对照组在脉间间隔20、80、200 ms时的配对脉搏指数差异无统计学意义(P> 0.05,双因素方差分析)。结论。结果提示,激活海马胶质谷氨酸转运体对海马CA1区基线突触反应和短期突触可塑性无影响。实际意义。考虑到神经胶质细胞在调节神经系统兴奋性和突触可塑性方面的作用,通过操纵神经胶质细胞来纠正神经系统的这些特征有助于治疗或预防神经系统疾病。本研究通过刺激谷氨酸摄取,评估了神经胶质细胞在海马突触空间谷氨酸稳态中的作用,对突触基本活性和短期突触可塑性的影响。
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