Nonrapid eye movement sleep is characterized by high-amplitude and low-frequency electroencephalography signals. These signals are thought to be produced by the synchronized activity of cortical neurons, demonstrating the alternating bursting (up) and resting (down) states. Here, such an activity is referred to as up-down oscillation (UDO). Previously, we discussed the importance of the Ca-dependent hyperpolarization pathway in the generation of UDO by simulating neuronal activity based on the Hodgkin-Huxley-type model. We herein focus on intracellular Na dynamics. The Na-centered model indicates that the activation of voltage-gated Na channels leads to intracellular Na accumulation, which in turn activates Na-dependent K (KNa) channels or Na/K ATPases, resulting in the down state. Activation kinetics of voltage-gated Na channels are important in shaping the UDO firing. Therefore, our model demonstrates that voltage-gated Na and KNa channels or Na/K ATPases are candidate pathways for UDO induction.
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http://dx.doi.org/10.1016/j.isci.2025.111904 | DOI Listing |
iScience
February 2025
Department of Systems Pharmacology, Graduate School of Medicine, The University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
Nonrapid eye movement sleep is characterized by high-amplitude and low-frequency electroencephalography signals. These signals are thought to be produced by the synchronized activity of cortical neurons, demonstrating the alternating bursting (up) and resting (down) states. Here, such an activity is referred to as up-down oscillation (UDO).
View Article and Find Full Text PDFNeuron
March 2025
Neuroscience Institute, Langone Medical Center, New York University, New York, NY, USA; Department of Physiology and Neuroscience, Langone Medical Center, New York University, New York, NY, USA; Department of Neurology, Langone Medical Center, New York University, New York, NY, USA. Electronic address:
Systems consolidation relies on coordination between hippocampal sharp-wave ripples (SWRs) and neocortical UP/DOWN states during sleep. However, whether this coupling exists across the neocortex and the mechanisms enabling it remains unknown. By combining electrophysiology in mouse hippocampus (HPC) and retrosplenial cortex (RSC) with wide-field imaging of the dorsal neocortex, we found spatially and temporally precise bi-directional hippocampo-neocortical interaction.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
January 2025
Division of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA 02115.
Sleep spindles are cortical electrical oscillations considered critical for memory consolidation and sleep stability. The timing and pattern of sleep spindles are likely to be important in driving synaptic plasticity during sleep as well as preventing disruption of sleep by sensory and internal stimuli. However, the relative importance of factors such as sleep depth, cortical up/down-state, and temporal clustering in governing sleep spindle dynamics remains poorly understood.
View Article and Find Full Text PDFbioRxiv
October 2024
Neuroscience Institute, Langone Medical Center, New York University, New York, NY, USA.
Cogn Neurodyn
August 2024
Department of Biotechnology, Bhupat and Mehta Jyoti School of Biosciences, Indian Institute of Technology Madras, Chennai, Tamil Nadu India.
Unlabelled: Working memory (WM) is considered as the scratchpad for reading, writing, and processing information necessary to perform cognitive tasks. The Basal Ganglia (BG) and Prefrontal Cortex are two important parts of the brain that are involved in WM functions, and both structures receive projections from dopaminergic nuclei. In this modelling study, we specifically focus on modelling the WM functions of the BG, the WM deficits in Parkinson's disease (PD) conditions, and the impact of dopamine deficiency on different kinds of WM functions.
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