A Design Principle for slow-wave sleep firing pattern with Na+dynamics

Author:

Sato Tomohide R.,Ode Koji L.,Kinoshita Fukuaki L.,Ueda Hiroki R.

Abstract

SUMMARYNon-rapid eye movement (NREM) sleep is characterized by electroencephalography (EEG) signals with high amplitude and low frequency. This signal is thought to originate from the synchronized activity of cortical neurons, showing the alternating bursting state (up state) and resting state (down state). This activity is termed as slow-wave sleep (SWS) firing pattern. We previously proposed the importance of Ca2+-dependent hyperpolarization pathway in generating this firing pattern by introducing the averaged-neuron (AN) model, which describes neuronal activity based on the Hodgkin-Huxley type model. In the AN model, Ca2+-dependent K+channels are involved in the transition from the up to the down state. Here we focus on the intracellular Na+dynamics which are not explicitly described in the AN model. A revised AN model, termed as Na+-centered AN (NAN) model, proposes that the activation of voltage-gated Na+channels leads to intracellular Na+accumulation, which in turn triggers the activation of Na+-dependent K+(KNa) channels or Na+/K+ATPases, resulting in the down state. Changes in the activation kinetics of voltage-gated Na+channels are important in shaping SWS firing pattern as well as explaining the inter-spike interval changes between SWS and AWAKE firing pattern. Mathematically, transition from the up state to the down state occurs in accordance with the change in the number of the fixed point in the dynamical system with the changes in the intracellular Na+concentration. The importance of Na+-dependent pathway is elucidated even with the coexistence of Ca2+-dependent pathway. Subsequent analysis with network model suggests that the result of averaged neuron model with Na+pathway can be extended to the population of neurons. Therefore, our model proposes that voltage-gated Na+channels and Na+-dependent K+channels or Na+/K+ATPases are also the candidate pathways for the generation of SWS firing pattern.

Publisher

Cold Spring Harbor Laboratory

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3