Evidence map›Paper›PMID 39555302›Full record

ArticleCognitive neurodynamics2024

Spike-spindle coupling during sleep and its mechanism explanation in childhood focal epilepsy.

Min Pan, Qiang Li, Jiangling Song, Duo Li, Rui Zhang

Abstract read
In one paragraph

Article in Cognitive neurodynamics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Min PanMedical Big Data Research Center, Northwest University, Xi'an, China.
Qiang LiMedical Big Data Research Center, Northwest University, Xi'an, China.
Jiangling SongMedical Big Data Research Center, Northwest University, Xi'an, China.
Duo LiMedical Big Data Research Center, Northwest University, Xi'an, China.
Rui ZhangMedical Big Data Research Center, Northwest University, Xi'an, China.ORCID 0000-0001-9547-2585

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Childhood focal epilepsy (CFE) is a serious neurological disorder characterized by epileptic seizures arising from a focal or multi-focal zone of the brain in clinics. During non-rapid eye movement (NREM) sleep stage, epileptiform discharges become frequent, and sleep spindles are generated through local interaction between thalamic neurons for CFE patients. Recent research has shown that epileptiform spikes significantly induce spindle oscillations within 1 s (say, spike-spindle coupling) during NREM sleep in focal epilepsy, which might damage cognitive function of epilepsy patients. However, the temporal interaction mechanism between spikes and spindles is lack of understanding. In this paper, we first develop a new thalamocortical model of CFE (CFE-TCM) by integrating M-type potassium current, persistent sodium current and NMDAR current into Costa model, where the three types of currents are important for modulating the excitability of thalamocortical system. Then we demonstrate in simulations that: (1) the temporal spike-spindle coupling oscillatory patterns do exist in real CFE-EEGs recorded in clinics; (2) the constructed model CFE-TCM has a capacity of generating spike-spindle coupling discharges, and the corresponding statistical results are consistent with those obtained from real EEGs; (3) the spike-spindle coupling discharges are mediated by the strength of long-range thalamus-cortex connections where the excitable projection from thalamocortical neuron in thalamus to pyramidal neuron in cortex takes a great role. The obtained results reveal that pathological spike-spindle coupling may be a potential marker of thalamocortical circuit dysfunction, which will provide a possible treatment strategy for disease progression and cognition impairment in focal epilepsy.

Indexed as

Long-range thalamus-cortex connectionM-type potassium currentNMDAR currentPersistent sodium currentSpike-spindle couplingThalamocortical neural mass model

Identifiers

PMID39555302
PMCPMC11564472

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.