Sleep, vigilance, and thermosensitivity
The regulation of sleep and wakefulness is well modeled with two underlying processes: a circadian and a homeostatic one. So far, the parameters and mechanisms of additional sleep-permissive and wake-promoting conditions have been largely overlooked. The present overview focuses on one of these conditions: the effect of skin temperature on the onset and maintenance of sleep, and alertness. Skin temperature is quite well suited to provide the brain with information on sleep-permissive and wake-promoting conditions because it changes with most if not all of them. Skin temperature changes with environmental heat and cold, but also with posture, environmental light, danger, nutritional status, pain, and stress. Its effect on the brain may thus moderate the efficacy by which the clock and homeostat manage to initiate or maintain sleep or wakefulness. The review provides a brief overview of the neuroanatomical pathways and physiological mechanisms by which skin temperature can affect the regulation of sleep and vigilance. In addition, current pitfalls and possibilities of practical applications for sleep enhancement are discussed, including the recent finding of impaired thermal comfort perception in insomniacs.
KeywordsSleep Vigilance Circadian rhythm Homeostatic regulation Thermoregulation Thermosensitivity Insomnia
In order to provide an intuitive idea on the focus of the present review on sleep and thermoregulation, one may try to imagine two situations likely familiar to most researchers and clinicians reading this review. The first situation is as follows. Consider a moment of considerable fatigue after a long working day while there is still that one manuscript that needs to be read and commented on today. What would be the best strategy to promote alertness and finish the job: reading it sitting at one’s desk, or rather lying down on the sofa to give in somewhat to the fatigue, and read it semi-supine? The second situation is also familiar to many of us. Imagine flying back home from a demanding conference, eager to catch a nap. How does trying to sleep in a sitting position compare to trying to sleep in a supine position? For most of us, answers to these questions come without even the slightest bit of doubt. If one has to stay awake, chances to do so successfully are better with sitting, and even more so with standing, as compared to lying down [13, 14, 18, 49]. If one desires to sleep on the other hand, most of us succeed much better when lying down [2, 62]. Although most sleep researchers agree with these answers, are they supported by current models on the regulation of sleep and alertness?
Sleep regulation: are a clock and an hourglass sufficient?
As discussed in detail in other papers in the present special issue and reviewed many times before, the core model of sleep–wake regulation consists of a circadian component and a homeostatic component [7, 19, 22]. The circadian (circa = about, dies = day) component refers to the clock of the brain. The central clock of our brain is located in the hypothalamic suprachiasmatic nucleus (SCN) and drives many physiological and behavioral rhythms including the promotion of sleep during one part of the circadian cycle and wakefulness during the other part , in humans respectively night and day. However, circadian processes are not limited to the central circadian pacemaker formed by the SCN. Indeed, molecular clock mechanisms are found in every single cell (reviewed in ). This is not surprising given the fact that the evolution of life on our rotating planet has always occurred in an environment with near-24-h cycles of light and darkness, and corresponding higher and lower environmental temperatures. Given this origin, it is also not surprising that both light and temperature can affect clock mechanisms at the cellular and systems level, as will be touched upon later [21, 84].
The homeostatic component refers to the hourglass of the brain. The longer we are awake, the stronger the pressure for sleep. While we are asleep, this pressure dissipates, and as soon as we wake up, the process starts all over again, just like turning an hourglass at every transition between sleep and wakefulness [1, 53, 88]. The neurobiological mechanisms underlying the hourglass are not characterized as well as the mechanisms of the clock are. As reviewed elsewhere in the present special issue and several times before, important roles have been assigned to adenosine , to an increase in synaptic density during wakefulness , and to cytokines .
Back to our question: how does the consensus model of sleep regulation account for the quite familiar experience that it is easier to stay awake in an upright position and easier to fall asleep in a supine position? Does this simple change of posture phase-shift our clock? Does it tilt the hourglass? Does it affect these processes at all? The answer seems to be a definitive no. The clock and hourglass model has brought us very far in understanding the regulation of sleep and wakefulness. Both components are necessary to understand the maintenance and transitions of states. They model it so well under comfortable, safe, and variance-limiting laboratory conditions that we tend to forget that the model may not necessarily be sufficient for a complete understanding of the maintenance and transitions of states, as we will argue below.
Sleep-permissive and wake-promoting conditions
In real life, sleep onset and maintenance also depend on whether some seemingly trivial yet crucial conditions are met, like having attained an appropriate posture. Being in a supine position is being in a sleep-permissive condition, whereas being upright is being in a wake-promoting condition [2, 13, 14, 18, 49, 62]. Posture is just one of several examples of permissive and promoting conditions. Are we as likely to maintain the state of sleep or wakefulness in a brightly lit versus dark environment ? And whatever state the clock and hourglass tells our sleep-regulating systems to implement, how easy are we going to fall asleep, or continue to sleep, in case of acute cold [65, 75], heat [37, 63], danger [16, 35], pain [26, 52], or stress [3, 92]? Just like the clock mechanisms are strongly rooted in evolution, so are the sensitivities to sleep-permissive and wake-promoting conditions: the odds for survival would be severely compromised if these were not effective. We plea that insights into the parameters and mechanisms of sleep-permissive and wake-promoting conditions are no less important for our understanding of sleep regulation and sleep disorders than insights into the mechanisms underlying the clock and hourglass are.
The present overview focuses on one of these conditions: the effect of skin temperature on the onset and maintenance of sleep, and alertness. Skin temperature is quite well suited to provide the brain with information on sleep-permissive and wake-promoting conditions because it changes with most if not all of them. Because the skin is rather poikilotherm, its temperature changes with environmental heat and cold. It changes also with posture [61, 78], environmental light [12, 80], anxiety , nutritional status , pain [36, 42, 54], and stress . Its effect on the brain may thus moderate the efficacy by which the clock and homeostat manage to initiate or maintain sleep or wakefulness.
Skin temperature is modulated by environmental and endogenous processes. The human skin is under the influence of environmental temperature. In addition, skin temperature depends on endogenous central and autonomic nervous system processes that actively regulate blood flow through the skin (reviewed in ). Variation in perfusion of the skin with the ~37°C blood thus results in an endogenous modulation of skin temperature. Information on skin temperature, measured with cold and warm receptors and conveyed through thermosensitive afferent pathways, reaches the brain in order to allow for thermoregulation . However, information on skin temperature does not only reach brain areas with a primary involvement in thermoregulation but also brain areas involved in other functions (reviewed in ).
Skin temperature and sleep–wake regulation
Indeed, several neuronal systems that are directly or indirectly involved in sleep–wake regulation are sensitive to temperature (reviewed in [84, 85, 86]). This is not surprising from an evolutionary perspective given that environmental temperature has a long history of affecting sleep–wake behavior. In the evolutionary older ectotherms, the behavioral relationship between temperature and vigilance level is relatively straightforward. Ectotherms require warming up by exposure to the radiation of the sun in order to become active. On the other hand, endotherms aim to maintain their core body temperature within a small range, which makes the relationship between temperature and vigilance more complex. The most studied organisms, humans and small furred mammals (such as rats, ground squirrels, and hamsters), mainly sleep during that part of the day when their core body temperature is low, and are most awake during the part of the day when their core body temperature is high, which resembles the behavior of ectotherms. But unlike ectotherms, their skin temperature is elevated during the sleep period due to an increase in skin blood flow in combination with behavior that limits heat loss through insulation by creating a warm microclimate, like covering and curling up. This results in an inverse relationship between core and skin temperature in everyday life, while in ectotherms, skin and core body temperature covary over time in phase. The question thus becomes more complicated: to what extent are the biological systems that are involved in sleep–wake rhythm regulation differentially affected by the normal variations in core temperature versus skin temperature?
As extensively reviewed elsewhere , several brain areas involved in sleep regulation are differentially sensitive to the local brain temperature which covaries with core temperature, versus skin temperature which shows an inverse relation to core temperature during the 24-h cycle. A key area that plays a key role in both sleep and temperature regulation is the preoptic area of the anterior hypothalamus. Animal studies indicate that both mild local warming of the area using a micro-thermode as well as mild skin warming using a wrap induce its neuronal fire patterns to resemble those of sleep and inhibit those associated with wakefulness [4, 57, 58]. The same was shown in the posterior hypothalamic area. Mild skin warming has also been associated with sleep-like activity in the cerebral cortex and midbrain reticular formation. Local brain warming has furthermore been shown to induce sleep-like firing patterns in the diagonal band but also wake-like firing patterns in the midbrain reticular formation and midline thalamic nuclei. A detailed description of the neuroanatomical pathways involved in the effect of skin temperature on vigilance regulation is beyond the scope of the present paper, and has been reviewed previously . Taken together, the effect of a mild increase in brain temperature may differentially drive different brain areas towards either a more sleep-like or a more wake-like firing pattern. The complex relationship between brain temperature and neuronal firing patterns makes an unequivocal sleep-promoting effect of mild increases in brain temperature unlikely. In contrast, the effect of a mild increase in skin temperature in general seemed to drive different brain areas towards more sleep-like firing patterns. If these findings can be translated to a real-life situation, a mild increase in skin temperature might promote sleep.
Next to these general functional anatomy considerations, how would core and skin temperature affect the specific functional anatomy that underlies the hourglass and clock of sleep regulation? Little is known on specific effects of temperature on the incompletely understood regulation of adenosine that is thought to be involved in the homeostatic aspect of sleep regulation. With respect to the much better understood clock-related systems, evidence has accumulated over the last decade to indicate that peripheral oscillators, including those in the brain (e.g., cerebral cortex), can be entrained by ambient temperature cycles [8, 9, 28]. On the other hand, such cycles do not appear to affect the intact SCN, the central clock of the brain. The SCN itself becomes sensitive to ambient temperature cycles only if communication between its neurons is restricted, as is the case in early development  or can be accomplished with application of tetrodotoxin . This is an interesting observation with respect to aging, where communication between SCN neurons is likely to be compromised because of low expression of vasoactive intestinal polypeptide, an essential factor in electrical synchronization of SCN neurons . In humans, the decrease in VIP occurs in a gender-specific way, i.e., in males mostly . Thus, it may be that temperature cycles have the capacity to enhance sleep–wake rhythms more prominently at high age, where rhythms are most vulnerable and associated with well-being .
Support for an effect of skin temperature on vigilance in humans
What is, in humans, the observational support for an association between skin temperature and vigilance, operationalized as the ability to initiate or maintain sleep or alert wakefulness? First, constant routine and forced desynchrony studies provide unequivocal observational support that people sleep best while they head towards the trough of their 24-h core body temperature and perform best around its peak . Constant routine protocols fix posture, activity, light, behavioral state, and food intake over a prolonged period of time. These normally give confounding effects because they coincide with transitions between wake and sleep or their preferred circadian phase of occurrence. In forced desynchrony protocols, sleep–wake cycles of more (e.g., 28 h) or less (e.g., 20 h) than 24 h are implemented. The endogenous biological clock cannot keep pace with these periods, so that, if continued long enough, effects of its near-24-h rhythms can be deconvolved from the effects of the imposed non-24-h rhythm. Unfortunately, because skin temperature was usually not measured during these studies, the relative contribution of the inversely related core and skin temperature changes to the variance in vigilance could not be evaluated. A number of studies that specifically investigated spontaneous or indirectly experimentally induced fluctuations in skin temperature, however, strongly support an association with vigilance. Healthy people fall asleep more easily if their skin temperature or bed temperature is higher [47, 48, 93]. The same association was shown for people with a vasospastic syndrome, who have a lower temperature of their hands and tend to have difficulties falling asleep , and for narcoleptic patients, where skin temperature is correlated to their daytime sleep propensity . With respect to the ability to maintain alert wakefulness, healthy people perform better during the troughs of their normal daytime skin temperature fluctuations . Preliminary findings in both healthy elderly people and demented elderly people also indicate more complaints on daytime sleepiness in those who have elevated daytime skin temperature .
Whereas in these studies proximal skin temperature has often been found to predict vigilance measures better than distal skin temperature, controlled laboratory studies suggest the reverse. Based on these controlled studies, it has been proposed that it may especially be the gradient between the temperatures measured at a distal and a proximal site that correlates most strongly with measures of vigilance [46, 47, 48, 49]. In these studies, subjects are in a semi-supine position that promotes skin blood flow and results in higher baseline skin temperatures. An important question to address in future research is to what extent mild fluctuations around a lower versus higher baseline skin temperature modify their association with fluctuations in vigilance levels.
All these correlational studies can be interpreted as merely indicating that skin temperature reflects an underlying process of vigilance regulation. What is the experimental support for a causal contribution of skin temperature to vigilance regulation? Controlled skin temperature manipulation studies using a water-perfused thermosuit indeed provide support for the notion that skin temperature modulates vigilance regulation, and more than core temperature does. It has been demonstrated in younger and older healthy adults, as well as in patients suffering from either insomnia or narcolepsy, that very mild skin cooling enhances sustained task performance and the ability to maintain wakefulness [34, 70], while mild skin warming facilitates sleep onset [67, 71] and promotes slow wave sleep and sleep maintenance [33, 69]. Skin temperature manipulations may thus even complement available research tools to experimentally affect slow cortical oscillations during sleep [55, 81]. Concertedly, these findings now provide strong support for a causal contribution of skin temperature to vigilance regulation, as was suggested from animal studies (reviewed in ).
Towards practical applications of sleep enhancement
Surprisingly, within a very small temperature range, it appears theoretically possible to impose a slightly warmer skin temperature, yet promoting rather than inhibiting heat loss and thus lowering skin temperature. In humans, the environmental temperature that the skin is exposed to strongly determines the volume of blood flowing through the skin vasculature, and thus the efficiency of exchanging heat from the body to the environment. The skin is a relatively good insulator, keeping the heat within the body up to an environmental temperature of about 33°C. However, it dramatically loses its heat-insulating properties and allows for a much more effective heat transfer to the environment once it is exposed to, and takes on, an environmental temperature of ~35°C [Fig. 2, 6, 29]. Thus, while the temperature gradient between the core and the environment decreases if the environment is warmed, the possibility to lose heat does not necessarily decrease and may even increase. The large increase in skin blood flow with this small increase in skin temperature effectively reduces the heat insulation properties the skin normally provides, and facilitates heat flow from the core to the environment. Thus, while the gradient between a core body temperature of 37°C and an environment of ~35°C is less than a gradient of 37°C versus 33°C, it may still be easier to reach lower core body temperatures because the insulating property of the skin is much reduced. Efforts to improve sleep by external heating should obtain feedback from the skin to create a closed loop manipulation, ensuring that it keeps the skin temperature within a range that still allows for the core body temperature to drop—settings which may even differ between individuals. Ultimately, this closed loop manipulation may lead to home-applicable versions of the methodology that showed efficacy in lab studies on young and elderly people without sleep complaints or suffering from insomnia or narcolepsy [33, 67, 69, 71].
Another, indirect, possibility to increase skin temperature during the sleep period without impeding the nocturnal drop in core body temperature is to make use of normal thermoregulatory mechanisms. This alternative to direct warming of the skin during the desired sleep period is to heat the body prior to sleep, for example, by exercising or taking a hot bath or sauna. Body heating activates heat dissipation for a duration that outlasts the heat stress, and consequently may keep skin blood flow higher for a few hours. Indeed, this indirect endogenous skin warming procedure has shown to improve subsequent sleep in several studies (reviewed in ). It is important to note that this sleep enhancement seems to occur mostly when the heat stress is annihilated, i.e., core temperature is no longer elevated, while skin temperature is still somewhat increased due to the overshoot in heat dissipation [10, 11, 20, 23, 24, 25, 40, 41, 44, 45, 76]. Thus, because of the restricted interval of increased sleep propensity, this procedure may be applied to enhance sleep onset and improve sleep in the first hours of the night. But it is unlikely to show an effect on complaints of early morning awakening, which may only be alleviated using direct skin temperature manipulation, as demonstrated in our lab studies .
An important question is whether skin temperature control to promote sleep would be necessary at all? If one examines time lapse videos of sleeping humans, it seems evident that people, during brief arousals from sleep, apply behavioral thermoregulation by kicking away the blankets or duvet to expose limbs to the cooler environment alternating with covering oneself to create a warm microclimate. But what if this behavior is somehow compromised? Or what if there is a deficit in the conscious or unconscious evaluation of the most appropriate temperature. It has never been evaluated systematically whether nocturnal thermoregulatory behavior differs between insomniacs and people without sleep complaints. We have an indication, however, that at least some phenotypes of insomnia may not recognize the most comfortable thermal microclimate that is conductive to sleep . Interestingly, these observations were recently supported by our finding  that the severity of their sleep complaints correlated with structural abnormalities in the part of the orbitofrontal cortex that is essential for the evaluation of comfort [27, 73].
Skin warming may thus be helpful for some insomnia phenotypes. However, we have unpublished data suggesting that in some insomniacs, metabolic heat production and heat-dissipating mechanisms are both elevated. In this case, further enhancement of heat dissipation may not be possible or useful. Any endeavor to evaluate the application of skin temperature control to promote sleep in insomniacs may thus profit from rigorous phenotype profiling and selection. Since the reliable long-term assessment of skin temperature in field studies has recently become as feasible as actigraphic assessments of sleep–wake rhythms has been for many years [82, 87, 90, 91], it would be of value to assess skin temperature profiles in large cohorts of people with and without sleep complaints. In addition, web-based surveys for multivariate assessment of insomnia phenotypes (www.sleepregistry.org, see ) could include extensive questioning on subjective thermosensitivity and behavioral thermoregulation. Concertedly, we estimate that it will be feasible within years to support the sleep of at least a subgroup of insomniacs using mild skin temperature manipulations.
This research is supported by Project NeuroSIPE 10738, of the Dutch Technology Foundation STW, which is part of the Netherlands Organization for Scientific Research (NWO) and partly funded by the Ministry of Economic Affairs, Agriculture and Innovation.
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