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J Neurophysiol 97: 3828-3840, 2007. First published April 4, 2007; doi:10.1152/jn.01184.2006
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Mathematical Model of Network Dynamics Governing Mouse Sleep–Wake Behavior

Cecilia G. Diniz Behn1, Emery N. Brown3, Thomas E. Scammell2 and Nancy J. Kopell1

1Department of Mathematics and Center for BioDynamics, Boston University; 2Department of Neurology, Beth Israel Deaconess Medical Center; and 3 Department of Anesthesia and Critical Care, Massachusetts General Hospital, Boston, Massachusetts

Submitted 7 November 2006; accepted in final form 2 April 2007

Recent work in experimental neurophysiology has identified distinct neuronal populations in the rodent brain stem and hypothalamus that selectively promote wake and sleep. Mutual inhibition between these cell groups has suggested the conceptual model of a sleep–wake switch that controls transitions between wake and sleep while minimizing time spent in intermediate states. By combining wake- and sleep-active populations with populations governing transitions between different stages of sleep, a "sleep–wake network" of neuronal populations may be defined. To better understand the dynamics inherent in this network, we created a model sleep–wake network composed of coupled relaxation oscillation equations. Mathematical analysis of the deterministic model provides insight into the dynamics underlying state transitions and predicts mechanisms for each transition type. With the addition of noise, the simulated sleep–wake behavior generated by the model reproduces many qualitative and quantitative features of mouse sleep–wake behavior. In particular, the existence of simulated brief awakenings is a unique feature of the model. In addition to capturing the experimentally observed qualitative difference between brief and sustained wake bouts, the model suggests distinct network mechanisms for the two types of wakefulness. Because circadian and other factors alter the fine architecture of sleep–wake behavior, this model provides a novel framework to explore dynamical principles that may underlie normal and pathologic sleep–wake physiology.


Address for reprint requests and other correspondence: C. Diniz Behn, Department of Neurology, Beth Israel Deaconess Medical Center, 77 Avenue Louis Pasteur, Boston, MA 02115 (E-mail: cbehn{at}bidmc.harvard.edu)




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