Humans and animals often exhibit brief awakenings from sleep (arousals), which are traditionally viewed as random disruptions of sleep caused by external stimuli or pathologic perturbations. However, our recent findings show that arousals exhibit complex temporal organization and scale-invariant behavior, characterized by a power-law probability distribution for their durations, while sleep stage durations exhibit exponential behavior. Such complex scale-invariant organization of the arousals makes it unlikely that they are merely a linear response to random external stimuli. The co-existence of both scale-invariant and exponential processes generated by a single regulatory mechanism has not been observed in physiological systems until now. Such co-existence resembles the dynamical features of non-equilibrium systems exhibiting self-organized criticality (SOC). Thus, we hypothesize that arousals are an integral part of sleep regulation and may be necessary to maintain and regulate healthy sleep by releasing accumulated excitations in the regulatory neuronal networks, following a SOC-type temporal organization. To address this hypothesis we propose to combine data from sleep physiology and bio-molecular/genetic experiments with modern concepts from statistical physics and the theory of complex networks. Utilizing the framework of SOC, our specific aim is: (i) to elucidate the mechanisms leading to scale-invariant organization of arousals during sleep;(ii) to uncover how pathologic conditions affect the SOC organization of arousals and sleep-stage transitions;(iii) to derive novel and more sensitive diagnostic markers of sleep disorders. We will analyze a large database from (i) healthy human subjects, and (ii) subjects with insomnia, narcolepsy, sleep apnea and other disorders;and (iii) from healthy wild type mice and rats. We will also utilize data from experimental animal models of various sleep disorders, where specific sleep-related neuronal groups and brain areas are targeted, to discern which key elements of the neurobiological interactions may be responsible for the emergence of SOC complexity in sleep dynamics at the system level. Establishing SOC-type complexity in sleep dynamics will challenge the current dominant homeostasis-based paradigm of sleep regulation, as it indicates the need of continuous fluctuations (arousals) over a broad range of time scales. How neuronal signaling interactions lead to SOC-type complexity at the system level is not known, and we will develop approaches based on the modern theory of scale-invariant networks to probe the role of the neuronal network topology in generating SOC in sleep dynamics.

Public Health Relevance

Brief awakenings from sleep (arousals) are traditionally viewed as disruptions of sleep, and their temporal dynamics as well as the underlying mechanisms are not well understood. We have recently discovered that the temporal organization of arousal episodes and sleep-stage durations in healthy sleep exhibit a self-organized criticality (SOC) behavior, which has not been previously reported in integrated physiological systems, and is not accounted for by the current homeostasis-based framework of sleep dynamics. This proposal focuses on identifying the basic control mechanisms leading to SOC behavior by utilizing available data from bio-molecular and genetic animal experiments as well as modern concepts from statistical physics applied to data from animal models and human polysomnographic recordings, that will allow us to link biochemical signaling pathways at the cellular level, through functional neuronal networks of sleep- and wake-promoting neurons, with sleep dynamics at the system level, and to derive novel clinical diagnostic and prognostic markers of sleep disorders.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
1R01HL098437-01A1
Application #
8108458
Study Section
Special Emphasis Panel (ZRG1-IFCN-E (02))
Program Officer
Laposky, Aaron D
Project Start
2011-04-05
Project End
2016-03-31
Budget Start
2011-04-05
Budget End
2012-03-31
Support Year
1
Fiscal Year
2011
Total Cost
$495,052
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code
02115
Dvir, Hila; Elbaz, Idan; Havlin, Shlomo et al. (2018) Neuronal noise as an origin of sleep arousals and its role in sudden infant death syndrome. Sci Adv 4:eaar6277
Xiong, Wanting; Faes, Luca; Ivanov, Plamen Ch (2017) Entropy measures, entropy estimators, and their performance in quantifying complex dynamics: Effects of artifacts, nonstationarity, and long-range correlations. Phys Rev E 95:062114
Gómez-Extremera, Manuel; Carpena, Pedro; Ivanov, Plamen Ch et al. (2016) Magnitude and sign of long-range correlated time series: Decomposition and surrogate signal generation. Phys Rev E 93:042201
Lin, Aijing; Liu, Kang K L; Bartsch, Ronny P et al. (2016) Delay-correlation landscape reveals characteristic time delays of brain rhythms and heart interactions. Philos Trans A Math Phys Eng Sci 374:
Li, Shan; Lin, Ruokuang; Bian, Chunhua et al. (2016) Model of the Dynamic Construction Process of Texts and Scaling Laws of Words Organization in Language Systems. PLoS One 11:e0168971
Liu, Kang K L; Bartsch, Ronny P; Ma, Qianli D Y et al. (2015) Major component analysis of dynamic networks of physiologic organ interactions. J Phys Conf Ser 640:
Liu, Kang K L; Bartsch, Ronny P; Lin, Aijing et al. (2015) Plasticity of brain wave network interactions and evolution across physiologic states. Front Neural Circuits 9:62
Bartsch, Ronny P; Liu, Kang K L; Bashan, Amir et al. (2015) Network Physiology: How Organ Systems Dynamically Interact. PLoS One 10:e0142143
Bartsch, Ronny P; Liu, Kang Kl; Ma, Qianli Dy et al. (2014) Three Independent Forms of Cardio-Respiratory Coupling: Transitions across Sleep Stages. Comput Cardiol (2010) 41:781-784
Lo, Chung-Chuan; Bartsch, Ronny P; Ivanov, Plamen Ch (2013) Asymmetry and Basic Pathways in Sleep-Stage Transitions. Europhys Lett 102:10008

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