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A Physiologically Based Model of Orexinergic Stabilization of Sleep and Wake

The orexinergic neurons of the lateral hypothalamus (Orx) are essential for regulating sleep-wake dynamics, and their loss causes narcolepsy, a disorder characterized by severe instability of sleep and wake states. However, the mechanisms through which Orx stabilize sleep and wake are not well under...

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Autores principales: Fulcher, Ben D., Phillips, Andrew J. K., Postnova, Svetlana, Robinson, Peter A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961294/
https://www.ncbi.nlm.nih.gov/pubmed/24651580
http://dx.doi.org/10.1371/journal.pone.0091982
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author Fulcher, Ben D.
Phillips, Andrew J. K.
Postnova, Svetlana
Robinson, Peter A.
author_facet Fulcher, Ben D.
Phillips, Andrew J. K.
Postnova, Svetlana
Robinson, Peter A.
author_sort Fulcher, Ben D.
collection PubMed
description The orexinergic neurons of the lateral hypothalamus (Orx) are essential for regulating sleep-wake dynamics, and their loss causes narcolepsy, a disorder characterized by severe instability of sleep and wake states. However, the mechanisms through which Orx stabilize sleep and wake are not well understood. In this work, an explanation of the stabilizing effects of Orx is presented using a quantitative model of important physiological connections between Orx and the sleep-wake switch. In addition to Orx and the sleep-wake switch, which is composed of mutually inhibitory wake-active monoaminergic neurons in brainstem and hypothalamus (MA) and the sleep-active ventrolateral preoptic neurons of the hypothalamus (VLPO), the model also includes the circadian and homeostatic sleep drives. It is shown that Orx stabilizes prolonged waking episodes via its excitatory input to MA and by relaying a circadian input to MA, thus sustaining MA firing activity during the circadian day. During sleep, both Orx and MA are inhibited by the VLPO, and the subsequent reduction in Orx input to the MA indirectly stabilizes sustained sleep episodes. Simulating a loss of Orx, the model produces dynamics resembling narcolepsy, including frequent transitions between states, reduced waking arousal levels, and a normal daily amount of total sleep. The model predicts a change in sleep timing with differences in orexin levels, with higher orexin levels delaying the normal sleep episode, suggesting that individual differences in Orx signaling may contribute to chronotype. Dynamics resembling sleep inertia also emerge from the model as a gradual sleep-to-wake transition on a timescale that varies with that of Orx dynamics. The quantitative, physiologically based model developed in this work thus provides a new explanation of how Orx stabilizes prolonged episodes of sleep and wake, and makes a range of experimentally testable predictions, including a role for Orx in chronotype and sleep inertia.
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spelling pubmed-39612942014-03-27 A Physiologically Based Model of Orexinergic Stabilization of Sleep and Wake Fulcher, Ben D. Phillips, Andrew J. K. Postnova, Svetlana Robinson, Peter A. PLoS One Research Article The orexinergic neurons of the lateral hypothalamus (Orx) are essential for regulating sleep-wake dynamics, and their loss causes narcolepsy, a disorder characterized by severe instability of sleep and wake states. However, the mechanisms through which Orx stabilize sleep and wake are not well understood. In this work, an explanation of the stabilizing effects of Orx is presented using a quantitative model of important physiological connections between Orx and the sleep-wake switch. In addition to Orx and the sleep-wake switch, which is composed of mutually inhibitory wake-active monoaminergic neurons in brainstem and hypothalamus (MA) and the sleep-active ventrolateral preoptic neurons of the hypothalamus (VLPO), the model also includes the circadian and homeostatic sleep drives. It is shown that Orx stabilizes prolonged waking episodes via its excitatory input to MA and by relaying a circadian input to MA, thus sustaining MA firing activity during the circadian day. During sleep, both Orx and MA are inhibited by the VLPO, and the subsequent reduction in Orx input to the MA indirectly stabilizes sustained sleep episodes. Simulating a loss of Orx, the model produces dynamics resembling narcolepsy, including frequent transitions between states, reduced waking arousal levels, and a normal daily amount of total sleep. The model predicts a change in sleep timing with differences in orexin levels, with higher orexin levels delaying the normal sleep episode, suggesting that individual differences in Orx signaling may contribute to chronotype. Dynamics resembling sleep inertia also emerge from the model as a gradual sleep-to-wake transition on a timescale that varies with that of Orx dynamics. The quantitative, physiologically based model developed in this work thus provides a new explanation of how Orx stabilizes prolonged episodes of sleep and wake, and makes a range of experimentally testable predictions, including a role for Orx in chronotype and sleep inertia. Public Library of Science 2014-03-20 /pmc/articles/PMC3961294/ /pubmed/24651580 http://dx.doi.org/10.1371/journal.pone.0091982 Text en © 2014 Fulcher et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fulcher, Ben D.
Phillips, Andrew J. K.
Postnova, Svetlana
Robinson, Peter A.
A Physiologically Based Model of Orexinergic Stabilization of Sleep and Wake
title A Physiologically Based Model of Orexinergic Stabilization of Sleep and Wake
title_full A Physiologically Based Model of Orexinergic Stabilization of Sleep and Wake
title_fullStr A Physiologically Based Model of Orexinergic Stabilization of Sleep and Wake
title_full_unstemmed A Physiologically Based Model of Orexinergic Stabilization of Sleep and Wake
title_short A Physiologically Based Model of Orexinergic Stabilization of Sleep and Wake
title_sort physiologically based model of orexinergic stabilization of sleep and wake
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961294/
https://www.ncbi.nlm.nih.gov/pubmed/24651580
http://dx.doi.org/10.1371/journal.pone.0091982
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