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Yang, D.-P.

Publications and source records attributed to Yang, D.-P..

2 recordsLinked to original sources

Mechanistic Modeling of Sleep-Wake Transitions via Circadian-Modulated Threshold Dynamics

Human sleep-wake cycles emerge from complex interactions between homeostatic sleep pressure and circadian rhythms. In this study, we extend the Phillips-Robinson model by introducing circadian-dependent dynamic thresholds for sleep and wake transitions, yielding a more physiologically grounded framework for sleep regulation. Using bifurcation analysis, we show that the transition from sustained wakefulness to rhythmic sleep-wake cycles is governed by a saddle-node on invariant circle (SNIC) bifurcation, and that these oscillations become entrained to external 24 h light-dark cues. We analytically derive circadian-modulated sleep and wake thresholds, revealing how the interaction between circadian and homeostatic drives governs sleep-wake transitions. Our model captures key physiological phenomena, including: (1) the onset and entrainment of sleep-wake rhythms, (2) immediate sleep onset and partial rebound following sleep deprivation, and (3) sleep fragmentation under shift work-like conditions. These results offer new mechanistic insights into how circadian misalignment alters sleep timing and quality. Together, our findings establish an updated theoretical framework for modeling sleep-wake regulation in both natural and disrupted environments, with implications for shift work management, sleep disorder interventions, and personalized chronotherapy. Author summarySleep and wakefulness are regulated by a complex interaction between circadian rhythms and homeostatic sleep pressure. While existing computational models have provided valuable insights, most rely on fixed or heuristic thresholds for sleep and wake transitions that lack direct physiological basis, limiting their ability to account for the full range of sleep behaviors-especially under disrupted conditions. In this study, we substantially update the computational framework in which sleep-wake transitions are governed by dynamically circadian-dependent thresholds. It captures how internal biological time shapes sleep patterns and explains key phenomena such as sleep rebound following deprivation and sleep fragmentation during shift work. It provides new insights into how circadian misalignment leads to sleep disorders and lays the groundwork for more effective, personalized interventions.

neuroscience↗

Pathological Pattern Formation in Absence Epilepsy: A Theoretical Framework to Unify Global and Focal Aspects

A physiology-based corticothalamic model is investigated with focal spatial heterogeneity, to unify global and focal aspects of absence epilepsy. Numerical and analytical calculations are employed to investigate the emergent spatiotemporal dynamics induced by focal activity as well as their underlying dynamical mechanisms. The spatiotemporal dynamics can be categorized into three scenarios: suppression, localization, and generalization of the focal activity, as summarized from a phase diagram vs. focal width and characteristic axon range. The corresponding temporal frequencies and spatial extents of wave activity during seizure generalization and localization agree well with experimental observations of global and focal aspects of absence epilepsy, respectively. The emergent seizure localization provide a biophysical explanation of the temporally higher frequency but spatially more localized cortical waves observed in genetic rat models that display characteristics of human absence epilepsy. Predictions are also presented for further experimental test.\n\nAuthor SummaryAbsence epilepsy is characterized by a sudden paroxysmal loss of consciousness accompanied by oscillatory activity propagating over many brain areas. Although primary generalized absence seizures are supported by the global corticothalamic system, converging experimental evidence supports a focal theory of absence epilepsy. Here we propose a dynamical mechanism to unify the global and focal aspects of absence epilepsy, with focal absence seizures associated with seizure localization, and the global ones associated with seizure generalization. Our corticothalamic model is used to investigate how seizure rhythms and spatial extents are related in these two different aspects of absence epilepsy. The results account for the difference of the experimentally observed seizure rhythms and spatial extents between humans and genetic rat models, which has previously been used to argue against the validity of such rats as animal models of absence epilepsy in humans.

neuroscience↗