Evidence map›Paper›PMID 26941611›Full record

ArticleFrontiers in neural circuits2016

Dynamic Analysis of the Conditional Oscillator Underlying Slow Waves in Thalamocortical Neurons.

François David, Vincenzo Crunelli, Nathalie Leresche, Régis C Lambert

Abstract read
In one paragraph

Article in Frontiers in neural circuits, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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

4 authors.

François DavidNeuroscience Division, School of Biosciences, Cardiff UniversityCardiff, UK; Lyon Neuroscience Research Center, Centre National de la Recherche Scientifique UMR 5292Lyon, France; Lyon Neuroscience Research Center, Institut National de la Santé et de la Recherche Médicale U1028Lyon, France; Faculté de Médecine, Université Claude BernardLyon, France; Sorbonne Universités, UPMC Université Paris 06, UM 119, Neuroscience Paris SeineParis, France; Centre National de la Recherche Scientifique, UMR 8246, Neuroscience Paris SeineParis, France; Institut National de la Santé et de la Recherche Médicale, U1130, Neuroscience Paris SeineParis, France.
Vincenzo CrunelliNeuroscience Division, School of Biosciences, Cardiff UniversityCardiff, UK; Department of Physiology and Biochemistry, University of MaltaMsida, Malta.
Nathalie LerescheSorbonne Universités, UPMC Université Paris 06, UM 119, Neuroscience Paris SeineParis, France; Centre National de la Recherche Scientifique, UMR 8246, Neuroscience Paris SeineParis, France; Institut National de la Santé et de la Recherche Médicale, U1130, Neuroscience Paris SeineParis, France.
Régis C LambertSorbonne Universités, UPMC Université Paris 06, UM 119, Neuroscience Paris SeineParis, France; Centre National de la Recherche Scientifique, UMR 8246, Neuroscience Paris SeineParis, France; Institut National de la Santé et de la Recherche Médicale, U1130, Neuroscience Paris SeineParis, France.

Funding

Wellcome Trust 91882
6 · The paper itself

Abstract

During non-REM sleep the EEG shows characteristics waves that are generated by the dynamic interactions between cortical and thalamic oscillators. In thalamic neurons, low-threshold T-type Ca(2+) channels play a pivotal role in almost every type of neuronal oscillations, including slow (< 1 Hz) waves, sleep spindles and delta waves. The transient opening of T channels gives rise to the low threshold spikes (LTSs), and associated high frequency bursts of action potentials, that are characteristically present during sleep spindles and delta waves, whereas the persistent opening of a small fraction of T channels, (i.e., ITwindow) is responsible for the membrane potential bistability underlying sleep slow oscillations. Surprisingly thalamocortical (TC) neurons express a very high density of T channels that largely exceed the amount required to generate LTSs and therefore, to support certain, if not all, sleep oscillations. Here, to clarify the relationship between T current density and sleep oscillations, we systematically investigated the impact of the T conductance level on the intrinsic rhythmic activities generated in TC neurons, combining in vitro experiments and TC neuron simulation. Using bifurcation analysis, we provide insights into the dynamical processes taking place at the transition between slow and delta oscillations. Our results show that although stable delta oscillations can be evoked with minimal T conductance, the full range of slow oscillation patterns, including groups of delta oscillations separated by Up states ("grouped-delta slow waves") requires a high density of T channels. Moreover, high levels of T conductance ensure the robustness of different types of slow oscillations.

Indexed as

Models, NeurologicalNonlinear Dynamics2-Amino-5-phosphonovalerate6-Cyano-7-nitroquinoxaline-2,3-dioneAnimalsBenzamidesCalciumCalcium Channel BlockersCatsCerebral CortexElectric StimulationExcitatory Amino Acid AntagonistsGABA AntagonistsGeniculate BodiesIn Vitro TechniquesMembrane Potentials2-Amino-5-phosphonovalerate3,5-dichloro-N-(1-(2,2-dimethyltetrahydropyran-4-ylmethyl)-4-fluoropiperidin-4-ylmethyl)benzamide6-Cyano-7-nitroquinoxaline-2,3-dioneBenzamidesCalciumCalcium Channel BlockersCGP 54626Excitatory Amino Acid AntagonistsGABA AntagonistsgabazineOrganophosphorus CompoundsPiperidinesPyridazinesbifurcationcomputational modelingdelta wavessleep slow wavethalamusT-type calcium channels

Identifiers

PMID26941611
PMCPMC4766279

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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.