| Autor: |
Borbély, Alexander, Tobler, Irene |
| Předmět: |
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| Zdroj: |
Clinical & Translational Neuroscience; Mar2024, Vol. 8 Issue 1, p5, 9p |
| Abstrakt: |
The two-process model of sleep regulation has served as a conceptual framework in the last four decades for understanding sleep physiology. In the 1970s, long-term recordings of sleep in rats were obtained thanks to EEG telemetry. NonREM sleep and REM sleep were found to differ in their time course and response to light-dark protocols. There were indications for their coupling to the circadian system, in particular the light-dark and the dark-light transitions. With the advent of quantitative EEG analysis, slow-wave activity in nonREM sleep was recognized as a sleep-wake-dependent variable. The term "sleep homeostasis" was coined to specify the regulated balance between sleep and waking. The regulatory homeostatic process was designated as "Process S". In the two-process model, its interaction with the circadian pacemaker "Process C" can account for sleep duration under various experimental protocols. Local, use-dependent slow-wave activity changes were demonstrated in both humans and rats by the selective, unilateral activation of a cortical region prior to sleep. Finding that rest in invertebrates has sleep-like regulatory properties opened a new realm of animal studies. Comparative sleep studies in a broad variety of animal species confirmed the validity of the basic concepts of the two-process model. Recent studies have addressed sleep-related changes of brain temperature as an indicator of brain metabolism; the application of the model to Drosophila; the divergence of cortical and subcortical states; and sleep in an increasing number of species and taxa. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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