Mus musculus
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA314957 | ENA |
REPOSITORIES: ENA
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Project description:This a model from the article:
A quantitative model of sleep-wake dynamics based on the physiology of the
brainstem ascending arousal system.
Phillips AJ, Robinson PA. J Biol Rhythms
2007 Apr;22(2):167-79 17440218
,
Abstract:
A quantitative, physiology-based model of the ascending arousal system is
developed, using continuum neuronal population modeling, which involves
averaging properties such as firing rates across neurons in each population. The
model includes the ventrolateral preoptic area (VLPO), where circadian and
homeostatic drives enter the system, the monoaminergic and cholinergic nuclei of
the ascending arousal system, and their interconnections. The human sleep-wake
cycle is governed by the activities of these nuclei, which modulate the
behavioral state of the brain via diffuse neuromodulatory projections. The model
parameters are not free since they correspond to physiological observables.
Approximate parameter bounds are obtained by requiring consistency with
physiological and behavioral measures, and the model replicates the human
sleep-wake cycle, with physiologically reasonable voltages and firing rates.
Mutual inhibition between the wake-promoting monoaminergic group and
sleep-promoting VLPO causes ;;flip-flop'' behavior, with most time spent in 2
stable steady states corresponding to wake and sleep, with transitions between
them on a timescale of a few minutes. The model predicts hysteresis in the
sleep-wake cycle, with a region of bistability of the wake and sleep states.
Reducing the monoaminergic-VLPO mutual inhibition results in a smaller
hysteresis loop. This makes the model more prone to wake-sleep transitions in
both directions and makes the states less distinguishable, as in narcolepsy. The
model behavior is robust across the constrained parameter ranges, but with
sufficient flexibility to describe a wide range of observed phenomena.
This model was taken from the CellML repository
and automatically converted to SBML.
The original model was:
Phillips AJ, Robinson PA. (2007) - version=1.0
The original CellML model was created by:
Catherine Lloyd
c.lloyd@auckland.ac.nz
The University of Auckland
This model originates from BioModels Database: A Database of Annotated Published Models (http://www.ebi.ac.uk/biomodels/). It is copyright (c) 2005-2011 The BioModels.net Team.
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In summary, you are entitled to use this encoded model in absolutely any manner you deem suitable, verbatim, or with modification, alone or embedded it in a larger context, redistribute it, commercially or not, in a restricted way or not..
To cite BioModels Database, please use: Li C, Donizelli M, Rodriguez N, Dharuri H, Endler L, Chelliah V, Li L, He E, Henry A, Stefan MI, Snoep JL, Hucka M, Le Novère N, Laibe C (2010) BioModels Database: An enhanced, curated and annotated resource for published quantitative kinetic models. BMC Syst Biol., 4:92.
2020-03-02 | BIOMD0000000917 | BioModels
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Project description:Identification of the mouse embryonic germ cell Dazl-/- transcriptome
2015-08-13 | GSE70358 | GEO