Though we have all determined
[1] that someone is asleep, or that we have been asleep, the gold-standard scientific verification of sleep requires the recording of signals, using
electrodes, arising from three different regions: (1) brainwave activity, (2) eye movement activity, and (3) muscle activ- ity. Collectively, these signals are grouped together under the blanket term “polysomnography” (PSG), meaning a readout (graph) of sleep (somnus) that is made up of multiple signals (poly). It was using this collection of measures that arguably the most important discovery in all of sleep research was made
in 1952 at the University of Chicago by Eugene Aserinsky (then a graduate student) and Professor Nathaniel Kleitman, famed for the Mam- moth Cave experiment discussed in chapter 2. Aserinsky had been carefully documenting the eye movement patterns of human infants during the day and night. He noticed that there were periods of sleep when the eyes would rapidly dart from side to side underneath their lids. Furthermore, these sleep phases were always accompanied by remarkably active brainwaves, almost identical to those observed from a brain that is wide awake. Sandwiching these earnest phases of active sleep were longer swaths of time when the eyes would calm and rest still. During these quiescent time periods, the brainwaves would also become calm, slowly ticking up and down
[2]. As if that weren’t strange enough, Aserinsky also observed that these two phases of slumber (sleep with eye movements, sleep with no eye movements) would repeat in a somewhat regular pattern throughout the night, over, and over, and over again. With classic professorial skepticism, his mentor, Kleitman, wanted to see the results replicated before he would entertain their validity. With his propensity for including his nearest and dearest in his experimenta- tion, he chose his infant daughter, Ester, for this investigation. The findings held up. At that moment Kleitman and Aserinsky realized the profound discovery they had made: humans don’t just sleep, but cycle through two completely different types of sleep. They named these sleep stages based on their defining ocular features: non–rapid eye movement, or NREM, sleep, and rapid eye movement, or REM, sleep. Together with the assistance of another graduate student of Kleitman’s at the time, William Dement, Kleit- man and Aserinsky further demonstrated that REM sleep, in which brain activity was almost identical to that when we are awake, was intimately con- nected to the experience we call dreaming, and is often described as dream sleep. NREM sleep received further dissection in the years thereafter, being subdivided into four separate stages, unimaginatively named NREM stages 1 to 4 (we sleep researchers are a creative bunch), increasing in their depth. Stages 3 and 4 are therefore the deepest stages of NREM sleep you expe- rience, with “depth” being defined as the increasing difficulty required to wake an individual out of NREM stages 3 and 4, compared with NREM stages 1 or 2.
In the years since Ester’s slumber revelation, we have learned that the two stages of sleep—NREM and REM—play out in a recurring, push-pull battle for brain domination across the night. The cerebral war between the two is won and lost every ninety minutes, fn2 ruled first by NREM sleep, followed by the comeback of REM sleep. No sooner has the battle finished than it starts anew, replaying every ninety minutes. Tracing this remarkable roller- coaster ebb and flow across the night reveals the quite beautiful cycling architecture of sleep, depicted in figure 8. On the vertical axis are the different brain states, with Wake at the top, then REM sleep, and then the descending stages of NREM sleep, stages 1 to 4. On the horizontal axis is time of night, starting on the left at about eleven p.m. through until seven a.m. on the right. The technical name for this graphic is a hypnogram (a sleep graph).