Du Mengmeng, Li Jiajia, Ying Wu, Yu Yuguo
State Key Laboratory for Strength and Vibration of Mechanical Structures, Xi'an Jiaotong University, Xi'an, 710049 China.
School of Aerospace Engineering, Xi'an Jiaotong University, Xi'an, 710049 China.
Cogn Neurodyn. 2022 Apr;16(2):411-423. doi: 10.1007/s11571-021-09706-w. Epub 2021 Sep 18.
Febrile seizure (FS) is a full-body convulsion caused by a high body temperature that affect young kids, however, how these most common of human seizures are generated by fever has not been known. One common observation is that cortical neurons become overexcited with abnormal running of sodium and potassium ions cross membrane in raised body temperature condition, Considering that astrocyte Kir4.1 channel play a critical role in maintaining extracellular homeostasis of ionic concentrations and electrochemical potentials of neurons by fast depletion of extracellular potassium ions, we examined here the potential role of temperature-dependent Kir4.1 channel in astrocytes in causing FS. We first built up a temperature-dependent computational model of the Kir4.1 channel in astrocytes and validated with experiments. We have then built up a neuron-astrocyte network and examine the role of the Kir4.1 channel in modulating neuronal firing dynamics as temperature increase. The numerical experiment demonstrated that the Kir4.1 channel function optimally in the body temperature around 37 °C in cleaning 'excessive' extracellular potassium ions during neuronal firing process, however, higher temperature deteriorates its cleaning function, while lower temperature slows down its cleaning efficiency. With the increase of temperature, neurons go through different stages of spiking dynamics from spontaneous slow oscillations, to tonic spiking, fast bursting oscillations, and eventually epileptic bursting. Thus, our study may provide a potential new mechanism that febrile seizures may be happened due to temperature-dependent functional disorders of Kir4.1 channel in astrocytes.
The online version contains supplementary material available at 10.1007/s11571-021-09706-w.
热性惊厥(FS)是由体温升高引起的幼儿全身性惊厥,然而,发热如何引发这些最常见的人类惊厥尚不清楚。一个常见的观察结果是,在体温升高的情况下,皮质神经元会因钠钾离子跨膜异常运行而变得过度兴奋。鉴于星形胶质细胞Kir4.1通道在通过快速消耗细胞外钾离子来维持神经元离子浓度和电化学电位的细胞外稳态中起关键作用,我们在此研究了星形胶质细胞中温度依赖性Kir4.1通道在引发FS中的潜在作用。我们首先建立了星形胶质细胞中Kir4.1通道的温度依赖性计算模型,并通过实验进行了验证。然后我们建立了一个神经元 - 星形胶质细胞网络,并研究了随着温度升高Kir4.1通道在调节神经元放电动力学中的作用。数值实验表明,Kir4.1通道在体温约37°C时功能最佳,可在神经元放电过程中清除“过量”的细胞外钾离子,然而,较高温度会使其清除功能恶化,而较低温度会减慢其清除效率。随着温度升高,神经元经历从自发缓慢振荡到强直性放电、快速爆发振荡,最终到癫痫样爆发的不同放电动力学阶段。因此,我们的研究可能提供了一种潜在的新机制,即热性惊厥可能是由于星形胶质细胞中Kir4.1通道的温度依赖性功能障碍所致。
在线版本包含可在10.1007/s11571-021-09706-w获取的补充材料。