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Microelectrode arrays for monitoring neural activity in neural stem cells with modulation by glutamate in vitro

机译:微电极阵列,用于监测神经干细胞中神经活性的神经活性,体外谷氨酸调节

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摘要

In this study, a 60-channel microelectrode array (MEA) was fabricated and used to monitor the neural spikes and local field potentials (LFPs) of neurons differentiated from rat neural stem cells in vitro. The neurons were grown on the MEA surface to detect neural signals. Glutamate (Glu) was used to modulate neural activity during experiments. To enhance detection performance, platinum nanoparticles were modified onto the microelectrode site surface. Glutamate stimulated neural spikes and LFPs were recorded using the MEA. The average spike amplitude was approximately 70 μV in the normal state. The spike amplitude increased by 29% from 70 μV to 90 μV with Glu modulation. The firing rate increased by 69% from 4.01 Hz to 6.8 Hz with Glu modulation. The LFP power increased from 326 μW in the normal state to 617 μW with Glu modulation in the 0–10 Hz frequency band. Data analysis shows that neural activity stimulated by Glu modulation was recorded experimentally at high temporal-spatial resolution. These results may provide a new neuron detection method, as well as further understanding of neural stem cell spike firing and associated mechanisms.
机译:在该研究中,制造了60通道微电极阵列(MEA)并用于监测从大鼠神经干细胞的神经元的神经尖峰和局部场电位(LFP)在体外分化。神经元在MEA表面上生长以检测神经信号。谷氨酸(Glu)用于调节实验期间的神经活动。为了提高检测性能,将铂纳米颗粒改性到微电极位点。使用MEA记录谷氨酸刺激的神经尖峰和LFP。在正常状态下平均峰值幅度约为70μV。尖峰幅度随Glu调制增加了29%从70μV至90μV增加了29%。烧制率从4.01 Hz增加到6.01升至6.8 Hz,Glu调制增加了69%。 LFP功率在0-10Hz频带中的Glu调制增加到617μW的326μW。数据分析表明,在高时的空间分辨率下通过Glu调制刺激刺激的神经活动。这些结果可以提供新的神经元检测方法,以及对神经干细胞尖峰烧制和相关机制的进一步理解。

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