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Sleep cycle

Oscillation between the slow-wave and REM phases of sleep

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Through Sleep, Wakefulness and Hormone

Characteristics

Electroencephalography shows the timing of sleep cycles by virtue of the marked distinction in brainwaves manifested during REM and non-REM sleep. Delta wave activity, correlating with slow-wave (deep) sleep, in particular shows regular oscillations throughout a good night's sleep. Secretions of various hormones, including renin, growth hormone, and prolactin, correlate positively with delta-wave activity, while secretion of thyroid-stimulating hormone correlates inversely. Heart rate variability, well known to increase during REM, predictably also correlates inversely with delta-wave oscillations over the ~90-minute cycle.

In order to determine in which stage of sleep the asleep subject is, electroencephalography is combined with other devices used for this differentiation. EMG (electromyography) is a crucial method to distinguish between sleep phases: for example, a decrease of muscle tone is in general a characteristic of the transition from wake to sleep, and during REM sleep, there is a state of muscle atonia (paralysis), resulting in an absence of signals in the EMG.

EOG (electrooculography), the measure of the eyes’ movement, is the third method used in the sleep architecture measurement; for example, REM sleep, as the name indicates, is characterized by a rapid eye movement pattern, visible thanks to the EOG.

Moreover, methods based on cardiorespiratory parameters are also effective in the analysis of sleep architecture—if they are associated with the other aforementioned measurements (such as electroencephalography, electrooculography and the electromyography).

Homeostatic functions, especially thermoregulation, occur normally during non-REM sleep, but not during REM sleep. Thus, during REM sleep, body temperature tends to drift away from its mean level, and during non-REM sleep, to return to normal. Alternation between the stages therefore maintains body temperature within an acceptable range.

In humans, the transition between non-REM and REM is abrupt; in other animals, it is less so.

Researchers have proposed different models to elucidate the undoubtedly complex rhythm of electrochemical processes that result in the regular alternation of REM and NREM sleep. Monoamines are active during NREMS, but not REMS, whereas acetylcholine is more active during REMS. The reciprocal interaction model proposed in the 1970s suggested a cyclic give-and-take between these two systems. More recent theories such as the "flip-flop" model, proposed in the 2000s, include the regulatory role of an inhibitory neurotransmitter gamma-aminobutyric acid (GABA).

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