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ABSTRACT: This a model from the article: This model was taken from the CellML repository and automatically converted to SBML. 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. 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..
Sleep deprivation in a quantitative physiologically based model of the ascendingarousal system.
Phillips AJ, Robinson PA. J Theor Biol 2008 Dec 21;255(4):413-23 18805427 ,
Abstract:
A physiologically based quantitative model of the human ascending arousal systemis used to study sleep deprivation after being calibrated on a small set ofexperimentally based criteria. The model includes the sleep-wake switch ofmutual inhibition between nuclei which use monoaminergic neuromodulators, andthe ventrolateral preoptic area. The system is driven by the circadian rhythmand sleep homeostasis. We use a small number of experimentally derived criteriato calibrate the model for sleep deprivation, then investigate model predictionsfor other experiments, demonstrating the scope of application. Calibration givesan improved parameter set, in which the form of the homeostatic drive is betterconstrained, and its weighting relative to the circadian drive is increased.Within the newly constrained parameter ranges, the model predicts repayment ofsleep debt consistent with experiment in both quantity and distribution,asymptoting to a maximum repayment for very long deprivations. Recovery is foundto depend on circadian phase, and the model predicts that it is most efficientto recover during normal sleeping phases of the circadian cycle, in terms of theamount of recovery sleep required. The form of the homeostatic drive suggeststhat periods of wake during recovery from sleep deprivation are phases ofrelative recovery, in the sense that the homeostatic drive continues to convergetoward baseline levels. This undermines the concept of sleep debt, and is inagreement with experimentally restricted recovery protocols. Finally, we compareour model to the two-process model, and demonstrate the power of physiologicallybased modeling by correctly predicting sleep latency times following deprivationfrom experimental data.
The original model was: Phillips AJ, Robinson PA. (2008) - version=1.0
The original CellML model was created by:
Catherine Lloyd
c.lloyd@auckland.ac.nz
The University of Auckland
To the extent possible under law, all copyright and related or neighbouring rights to this encoded model have been dedicated to the public domain worldwide. Please refer to CC0 Public Domain Dedication for more information.
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.
ORGANISM(S): Homo sapiens
SUBMITTER: Camille Laibe
PROVIDER: MODEL1006230115 | biostudies-other |
SECONDARY ACCESSION(S): 18805427
REPOSITORIES: biostudies-other

Journal of theoretical biology 20080829 4
A physiologically based quantitative model of the human ascending arousal system is used to study sleep deprivation after being calibrated on a small set of experimentally based criteria. The model includes the sleep-wake switch of mutual inhibition between nuclei which use monoaminergic neuromodulators, and the ventrolateral preoptic area. The system is driven by the circadian rhythm and sleep homeostasis. We use a small number of experimentally derived criteria to calibrate the model for sleep ...[more]