We have shown that cutaneous cooling-sensitive receptors can work as thermostats of skin temperature against cooling. However, molecule of the thermostat is not known. Here, we studied whether cooling-sensitive TRPM8 channels act as thermostats. TRPM8 in HEK293 cells generated output (y) when temperature (T) was below threshold of 28.4°C. Output (y) is given by two equations: At T >28.4°C, y = 0; At T <28.4°C, y = -k(T – 28.4°C). These equations show that TRPM8 is directional comparator to elicits output (y) depending on negative value of thermal difference (ΔT = T – 28.4°C). If negative ΔT-dependent output of TRPM8 in the skin induces responses to warm the skin for minimizing ΔT recursively, TRPM8 acts as thermostats against cooling. With TRPM8-deficient mice, we explored whether TRPM8 induces responses to warm the skin against cooling. In behavioral regulation, when room temperature was 10°C, TRPM8 induced behavior to move to heated floor (35°C) for warming the sole skin. In autonomic regulation, TRPM8 induced activities of thermogenic brown adipose tissue (BAT) against cooling. When menthol was applied to the whole trunk skin at neutral room temperature (27°C), TRPM8 induced a rise in core temperature, which warmed the trunk skin slightly. In contrast, when room was cooled from 27 to 10°C, TRPM8 induced a small rise in core temperature, but skin temperature was severely reduced in both TRPM8-deficient and wild-type mice by a large heat leak to the surroundings. This shows that TRPM8-driven endothermic system is less effective for maintenance of skin temperature against cooling. In conclusion, we found that TRPM8 is molecule of thermostat of skin temperature against cooling.
Citation: Tajino K, Hosokawa H, Maegawa S, Matsumura K, Dhaka A, Kobayashi S (2011) Cooling-Sensitive TRPM8 Is Thermostat of Skin Temperature against Cooling. PLoS ONE 6(3): e17504. https://doi.org/10.1371/journal.pone.0017504
Editor: Steven Barnes, Dalhousie University, Canada
Received: October 10, 2010; Accepted: February 6, 2011; Published: March 2, 2011
Copyright: © 2011 Tajino et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was supported by the Ministry of Education, Science, Sports and Culture and Technology Grant-in-Aid for Scientific Research. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
In mammals, thermostat is a key device to maintain body temperature against changes in ambient temperatures. Many investigators have studied thermostats , , , , , . Since Adrian , it has been assumed that thermo receptors are transducers (or sensors) that change temperature into the firing-rate code of impulse trains, travelling to the brain. Along this line, a target neuron receiving impulses from thermal receptors has been assumed to be “thermostat” that compares skin temperature with a set-point temperature at the level of the firing-rate code, and generates impulses as drive signal inducing thermoregulatory responses , , , .
If thermo receptors are transducers of temperature, their outputs should be related to temperature strictly. However, output of thermo receptors shows adaptation , , , , , even when temperature is constant. In addition, receptors show threshold response to temperature changes , . Moreover, TRPM8, a member of thermo TRP channel family , responds to menthol and icilin as well as temperature , . These results deny the assumption that receptors are transducers. Therefore, it is impossible for cerebral target neurons to detect skin temperature from afferent impulses sent from cooling-sensitive receptors. In fact, the “thermostat” neuron hypothesized in the brain , , ,  has not been found. By lack of the “thermostat”, regulation of skin temperature is not explained.
In contrast, we have shown that cutaneous cooling-sensitive receptor itself can act as thermostat, comparing skin temperature with its threshold temperature , . Single-channel recording shows that channel activities appear when temperature is lower than threshold temperature . These results indicate that phase transition is a biological direct method for comparison, different from artificial indirect one using a code. If cooling-induced activities of receptors elicit responses to warm the skin recursively, a negative feedback loop is formed for regulation of skin temperature against cooling . However, molecule of the thermostat has not been clarified.
Recently, cooling- and menthol-sensitive TRPM8 ,  has been identified. TRPM8 is expressed in C and Aδ sensory fibers ,  of cutaneous sensory nerves , . Experiments of TRPM8-deficient mice show that TRPM8 is required for cold sensation , , . Menthol application to the whole trunk skin  and intravenous menthol injection  induce behavioral responses to warm the skin. In contrast, TRPM8-induced autonomic thermoregulatory responses are not fully analyzed , , . Here, with TRPM8-deficient mice, we studied whether TRPM8 in the skin induces behavioral and autonomic responses to warm skin against room cooling.
TRPM8 is comparator, but not transducer
We examined thermal responses of TRPM8 channels expressed in HEK293 cells by calcium imaging . When temperature (T) was decreased slowly from 38 to 10°C (Fig. 1B), activities (y) of TRPM8 appeared at threshold temperature (mean, 28.4°C), and increased with a fall in temperature, consistent with prior studies , , . To explore a role of TRPM8, we schematically showed relationship between output (y) and temperature (T) in Fig. 1C. Due to the threshold response, output (y) is expressed by two equations:
(A, B) Ca2+ level (ratio) in five HEK293 cells expressing TRPM8. When temperature (T) was decreased slowly from 38 to 10°C (B), activities (output, y) of TRPM8 appeared at threshold temperature (28.4±0.5°C, mean ± SEM; n = 5) and increased with a fall in temperature. (C) Relationship between output (y) and temperature (T). Threshold response in (A) is shown approximately by two lines (green), which are expressed by two linear equations. When T is above 28.4°C, output (y) is 0. When T is below 28.4°C, output (y) = -k(T – 28.4°C). For explanation of the automatic control theory, thermal difference, ΔT ( = T – 28.4°C), is defined. When T is higher than 28.4°C, ΔT is positive. When T is lower than 28.4°C, ΔT is negative. Thus, y increases with expansion of negative ΔT. (D) Representation of TRPM8 by a cooling-sensitive switch. When ΔT is positive, this switch is turned off. When ΔT is negative, this switch is turned on and y increases with expansion of negative ΔT as shown in C.
Threshold temperature (28.4°C) is constant specific to TRPM8, and T is variable applied to TRPM8. In Equation 2, -k (<0) is a slope constant. Two equations show that TRPM8 has silent (Equation 1) and active (Equation 2) phases, and that phase transition occurs at 28.4°C . In terms of control theory, TRPM8 functions as directional comparator judging whether T is lower than 28.4°C, and generates output (y) proportionately with a negative thermal difference (ΔT = T – 28.4°C). For instance, when T is 22.4°C, TRPM8 enters active phase (Equation 2), and generates output (y) according to −6°C.
To aid comprehension, we symbolically show TRPM8 by a cooling-sensitive switch (Fig. 1D). At ΔT >0°C, this switch is turned off. At ΔT <0°C, this switch is turned on and output (y) increases with a fall in T from 28.4°C (Fig. 1C). In sensory neurons, output of sensory receptors generates receptor potential , eliciting impulse trains on sensory nerves . If negative ΔT-dependent impulse activities induce thermoregulatory responses to warm the skin for minimizing ΔT recursively, TRPM8 switch acts as thermostats of skin temperature having 28.4°C as set-point temperature against cooling . Then, intensity of the thermoregulatory activities (e.g., cold sensation and BAT activities) increases proportionately with expansion of ΔT, which corresponds to the proportional control in technology .
TRPM8 is also activated by menthol, when menthol concentration is higher than threshold level of 20 µM . This shows that TRPM8 acts as directional comparator of menthol concentration, generating output (y) depending on the positive difference from 20 µM to menthol concentration. In addition, TRPM8 is activated by icilin, when its concentration is higher than 0.1 µM . These properties indicate that TRPM8 are polymodal comparator of several kinds of stimuli. In later experiments, menthol is applied to the skin to explore TRPM8-driven thermogenic activities at neutral temperature . It should be notified, however, that even when menthol-induced activities of TRPM8 elicits responses to warm the skin, negative feedback loops are not formed, because responses to warm the skin do not reduce menthol concentration in the skin.
In contrast, if TRPM8 is transducer of temperature, output (y) of TRPM8 should be expressed by one continuous function of T , In fact, in the transducer hypothesis , threshold responses of sensory receptors were not described at all. However, threshold response (Fig. 1) is essential feature of TRPM8 , , , and output (y) is not expressed by one function of T. Moreover, output of TRPM8 is changed by menthol, icilin and other chemicals, even when T is constant , , . When menthol and T changes are applied in turn, output of TRPM8 shows complicated trace, different from T . Thus, target neurons can hardly detect skin temperature from impulses sent from TRPM8. These results reject the hypothesis that the “thermostat” of skin temperature is present in the brain , , .
TRPM8-driven behavior for warming the sole skin against room cooling
We examined whether output of TRPM8 induces behavior for warming the sole skin for regulation of skin temperature against cooling (Fig. 2). A free-moving mouse was placed in a cage with two floor temperatures for thermal preference test. When room temperature was neutral (27°C), stay time on 35°C floor was similar between wild-type and TRPM8-deficient mice, showing that TRPM8 is not involved in this behavior at 27°C. When room temperature was 10°C, stay time on 35°C floor was increased in both mice. However, stay time on 35°C floor in wild-type mice was longer than that in TRPM8-deficient mice. This indicates that TRPM8 comparators induce heat-seeking behavior for warming the sole skin against room cooling. This heat-seeking behavior corresponds to TRPM8-induced cold sensation , , , showing that TRPM8-induced cold sensation triggers the behavior for warming the sole skin. Cooling-induced TRPM8-independent behavior seems to be responses induced by non-TRPM8 receptors . These results show that TRPM8 comparators work as thermostats of skin temperature, inducing behaviors for warming the sole skin against cooling.
When room temperature was neutral (27°C), stay time on 35°C floor was not different between wild-type and TRPM8-deficient mice. At 10°C, stay time on 35°C floor was increased in both mice. However, stay time on 35°C floor in wild-type mice was longer than that in TRPM8-deficient mice (n = 8 mice each).
TRPM8-driven autonomic responses for warming the skin against cooling
TRPM8–induced activities of thermogenic BAT.
Pathways from cooling-sensitive receptors to thermogenic brown adipose tissues (BAT) are well characterized , . We examined whether TRPM8 channels induce BAT activities against room cooling (Fig. 3). To study cooling-induced BAT activation, mice were put at 10 or 27°C for 1h. When room temperature was 27°C, fluorescence of UCP1 was low in both TRPM8-deficient and wild-type mice (Fig. 3A, C). When room temperature was 10°C, UCP1 signals were increased in both mice (Fig. 3B, D), but the signal strength in wild-type mice was higher than that of TRPM8-deficient mice (Fig. 3B, D). To confirm this observation, we examined cooling-induced activities in phosphorylated NFkB (pNFkB) in nuclei, as a marker of BAT cell activities , . At 27°C (Fig. 3E, G), fluorescence of pNFkB was detected in neither TRPM8-deficient nor wild-type mice. At 10°C, the number of pNFkB-positive nuclei was increased in both mice (Fig. 3F, H), but the ratio of the number of pNFkB-positive nuclei to all nuclei in wild-type mice was higher than that in TRPM8-deficient mice (Fig. 3I). These results show that TRPM8 induces activities of thermogenic BAT used for warming the skin in response to cooling.
(A–D) Fluorescence signal of UCP1 in BAT. At 27°C, UCP1 signal was low in both mice (A, C). When room temperature was 10°C, UCP1 signal was increased in both mice (B, D). However, UCP1 signal in wild-type mice (B) was largely enhanced, compared to that in TRPM8-deficient mice (D). Scale bar = 50 µm. (E–H) Fluorescence signals of pNFkB in BAT nuclei. Cell nuclei were represented by red. At 27°C, fluorescent signals of pNFkB were not observed in both mice (E, G). At 10°C, the number of pNFkB positive nuclei (yellow) was increased in both mice (F, H). (I) Ratio of pNFkB-positive nuclei to all nuclei in BAT, counted from data as exemplified by E–H. Ratio was obtained in a field containing about 100 nuclei (n = 10 fields from 2 mice). The ratio of pNFkB-positive nuclei in wild-type mice was higher than that of TRPM8-deficint mice at 10°C.
Menthol- and cooling-induced TRPM8-driven thermogenic responses.
We examined whether TRPM8 in the skin induces thermogenic responses for warming the skin. When room temperature was 27°C, core temperature was 36.8°C and skin temperature was 34.2°C in both mice (Fig. 4). This shows that TRPM8 is not involved in maintaining normal body temperatures at 27°C, consistent with the earlier study . When menthol was applied to the whole trunk skin of mice at 27°C (Fig. 4A,B, arrows), TRPM8-dependent rise occurred in core (1.3°C) and skin temperatures (0.4°C).
(A, B) Menthol-induced changes in core and skin temperatures, drawn in different temperature scales. When menthol was applied to the whole trunk skin (arrows) at 27°C (B), TRPM8-dependent rise in core temperature (1.3°C) and in skin temperature (0.4°C) occurred (n = 10 mice each). (C, D) Room cooling-induced changes in core and skin temperatures. Core temperatures were drawn in different temperature scales. When room temperature was decreased from 27 to 10°C (D), TRPM8-dependent small rise (1.0°C) occurred in core temperature (C, D), but skin temperatures were severely decreased from 34.2 to 24.1°C in both TRPM8-deficient and wild-type mice (n = 8 mice each).
In contrast, when room was cooled from 27 to 10°C (Fig. 4C, D), core temperature of TRPM8-deficient mice was decreased (Fig. 4C), but that of wild-type mice was increased slightly. The TRPM8-dependent difference (1.0°C) reflects TRPM8-induced thermogenesis in the core. By the same room cooling, however, skin temperature was decreased severely from 34.2°C to 24.1°C in both mice (Fig. 4D), as if regulation is not functioning. Room cooling-induced decrease in skin temperature in wild-type mice is similar to the earlier study of rabbits . These results indicate that TRPM8-induced thermogenesis in the core is not powerful enough to warm the skin against cooling.
TRPM8 is not transducer of temperature
It has generally been assumed that a sensory receptor is transducer that changes physical quantity into the firing-rate code of nerve impulses, and that sensation appears by decoding the code . Along this line, a target neuron receiving impulses sent from thermo receptors has been assumed to be the “thermostat” that compares skin temperature with a set-point temperature at the code level , , , , .
However, the present study of TRPM8 shows that the above assumptions are not valid as a whole. TRPM8 is a polymodal receptor, responding to temperature, menthol, icilin and other chemicals , , , . This is strong evidence to reject the view that TRPM8 is transducer of temperature, because TRPM8 does not respond to skin temperature solely. From the very beginning, the view that a mouse measures skin temperature with receptor is inadequate, for measurement is done exclusively by a person who knows the meaning of temperature (e.g., 28.4°C) and the principle of measurement. Thus, the hypothesis that a cerebral target neuron is the “thermostat” of skin temperature , , ,  is not valid.
Temperature (e.g., 22.4°C) or menthol concentration (e.g., 100 µM) is physical quantity, and completely different from subjective feeling that the skin is cold. Therefore, the view that temperature or menthol concentration is transformed into cold sensation by coding-decoding system is not reasonable.
TRPM8 is thermostat of skin temperature
In contrast, the present study shows that TRPM8 is polymodal comparator of temperature, menthol concentration and icilin concentration. The present experiments show that output of TRPM8 induces responses to warm the skin, which indicates that TRPM8 acts as thermostat of the skin temperature against cooling (Fig. 5).
Cooling-sensitive TRPM8 is directional comparator of skin temperatures, inducing output (y) when ΔT ( = T – 28.4°C) is negative (Fig. 1). If negative ΔT-dependent output (y) induces thermoregulatory responses to warm the skin recursively, negative feedback loops having 28.4°C as set-point temperature are formed and TRPM8 functions as thermostat for minimizing ΔT against cooling. In behavioral regulation, when room is cooled, TRPM8 induces behavior to move to heated floor to warm the sole skin, which effectively maintains temperature of the sole skin against cooling. In autonomic regulation, when room is cooled, TRPM8 induces a small rise in core temperature, but skin temperature is severely decreased, as if regulation of skin temperature is not functioning.
TRPM8-induced afferent impulses are drive signals, which do not convey a code for skin temperature to target neurons. Then, how is low skin temperature related to cold sensation? TRPM8-induced impulses should excite a cerebral target neuron involved in cold sensation, which triggers behavior to warm sole skin. Thus, we assume that information to induce cold sensation is innately stored in a target neuron. If not stored, cold sensation would not be elicited even when a target neuron is excited by arriving impulses. Electric stimulations of local areas of the somatosensory cortex in conscious persons induce feeling that various spots of the whole-body skin are touched . This famous experiment supports the present assumption that information to induce cold sensation is stored in a target neuron. Cell theory states that a cell is the basic unit for structure and function of all plants and animals , which gives the basis for the modern cell biology . This cell theory also supports the present assumption that information to induce cold sensation is stored in a target neuron, because cold sensation is a critical function to survive in low ambient temperatures. These explanations are also applicable to menthol- ,  and icilin-induced cold sensation .
In autonomic regulation, when room is cooled deeply, the skin temperature is severely decreased in both mice (Figs. 4), as if regulation of the skin temperature is not functioning. This is an unexpected finding that TRPM8-induced autonomic responses are less powerful to maintain the skin temperature against cooling. To maintain skin temperature against cooling (Fig. 4), TRPM8-induced thermogenesis should warm the core drastically. However, an excessive rise in core temperature is harmful for mice. Thus, TRPM8-induced autonomic regulation of skin temperature has limited power in nature.
Many investigators have been interested in homeostasis of core temperature in mammals , , , . When room temperature is decreased from 27 to 10°C (Fig. 4D), skin temperature is decreased from 34.2°C to 24.1°C but core temperature is maintained near 36.5°C in both mice. The difference between core temperature and room temperatures is as high as 26°C. Thus, there should be thermostat working for homeostasis of core temperature. Intraperitoneal injection of 5′-AMP induces torpor-like response, in which core temperature is reduced from normal level to ambient temperature . This suggests that autonomic thermoregulatory system of core temperature is a device inhibited by 5′-AMP. However, the thermostat of core temperature remains unresolved.
Materials and Methods
TRPM8 (−/−) and TRPM8 (+/+) mice were obtained by breeding of TRPM8 (+/−) and TRPM8 (+/−) mice. Genotypes of mice were checked by allele specific PCR from tail genomic DNA . TRPM8-deficient and wild-type mice were housed under standard conditions (27°C; 12 h light/dark cycle; lights on at 6:00 a.m.) with food and water ad libitum. Male mice (2–6 months old) were used for experiments. All protocols were approved by Animal Research Committee of Kyoto University (Approval ID: Graduate School of Informatics 19-4).
Ratiometric calcium imaging
Doxycycline-inducible TRPM8-expressing HEK293 cells were established by Flp-In T-Rex system (Clontech, La jolla, CA), as described previously . Briefly, TRPM8-expressing cells on a collagen-I-coated coverslip were loaded with 2 µM Fura-2 AM. After washing with Krebs' solution, these cells on a coverslip was placed on a recording chamber mounted on the stage of fluorescence microscope (BS50WI, Olympus). With a digital image analysis system (AQUACOSMOS; Hamamatsu Photonics, Hamamatsu), intracellular Ca2+ ion concentration was measured by Fura-2 fluorescence ratio (F340/F380, excitation 340/380 nm and emission 510 nm), and displayed as TRPM8 activity.
A plastic cage (16 cm ×27 cm) was placed in the incubator. Floor of a cage was divided into two zones. One half (16 cm ×13.5 cm) was kept at 35°C with a heating pad placed under the cage and the other half was unheated. A mouse was transferred to the center of a test cage. Behavior was recorded by a digital video camera (30 frames/s) for 30 min. Time on 35°C floor (%) was measured with Image J for last 20 min.
We used UCP1 and pNFkB as markers of BAT activation. UCP1 is a protein for heat production in BAT . Localization of pNFkB is related to BAT activation , . To study cooling-induced BAT activation, mice were put at 10 or 27°C for 1 h. After anesthesia with pentobarbital, BAT was harvested. BAT tissues were transferred into OCT compounds (Sakura, Tokyo, JAPAN), frozen, and sectioned (20 µm-thick) with a cryostat. Sections were fixed in 10% (v/v) formalin in 0.1 M phosphate-buffered saline (PBS) for 10 min. After washing with 0.1 M PBS, these sections were blocked for 30 min with 10% (v/v) normal donkey serum in 0.1 M PBS containing 0.2% Triton X-100. BAT sections were incubated with anti-UCP1 antibody (1∶1000, CHEMICON, Themecula, CA) or rabbit anti-pNFkB p65 (Ser 276) antibody (1∶100, Cell Signaling Technology). After washing, sections were incubated with AlexaFluor 488-conjugated anti-rabbit IgG (H+L) (1∶1000, Molecular Probes, Eugene, OR) for 2 h at room temperature. Cell nuclei in BAT were visualized with Hoechst 33342 (1∶50000, invitrogen, Eugene, OR). Fluorescent images of BAT sections were captured by fluorescence microscope (Nikon ECLIPSE E600).
Temperature measurement and stimulation
Mice were implanted with E-mitter probe (minimitter, Bent, OR) in peritoneal cavity under pentobarbital anesthesia (70 mg/kg). 7 to 14 days after implantation, abdominal temperature was measured as core temperature. Mean temperature of the whole back skin was detected with thermography (Thermotracer TH3100MR, NEC San-ei Instrum, Kyoto, Japan) as skin temperature. By using anesthetized mice (n = 5), skin temperature of a thermography (15–33°C for room cooling experiment and 30–35°C for menthol application experiment) was calibrated with that of a thermocouple fixed on the back lumber with a tape.
Free-moving mice were put in an incubator (CRB-41, HITACHI; 62 cm ×50 cm ×132 cm) with a built-in regulator, and temperature in the incubator was used as room temperature. For thermal stimulation, room temperature was decreased from 27°C (neutral temperature) to 10°C. Room temperature was sampled every 10 min.
For menthol application, mice were anesthetized with 5% isoflurane for 30 sec. Menthol (l-menthol 10% w/v (640 mM), Wako, Japan) in ethanol was applied once to their whole trunk skin with paper (Kimwipes 6×5 cm) soaked with 600 µl solution of menthol.
Conceived and designed the experiments: KT HH SM KM SK. Performed the experiments: KT HH. Analyzed the data: KT. Contributed reagents/materials/analysis tools: AD. Wrote the paper: KT SK.
- 1. Hardy JD (1961) Physiology of Temperature Regulation. Physiological Reviews 41: 521–&.
- 2. Benzinger TH (1969) Heat regulation: homeostasis of central temperature in man. Physiol Rev 49: 671–759.
- 3. Mitchell D, Snellen JW, Atkins AR (1970) Thermoregulation during fever: change of set-point or change of gain. Pflugers Arch 321: 293–302.
- 4. Bligh J (1973) Temperature Regulation in Mammals and other Vertebrates: North-Holland.
- 5. Satinoff E (1978) Neural organization and evolution of thermal regulation in mammals. Science 201: 16–22.
- 6. Hensel H (1981) Thermoreception and temperature regulation. New York: Academic Press.
- 7. Adrian ED (1928) The basis of sensation. London: Christophers.
- 8. Hensel H (1973) Neural processes in thermoregulation. Physiol Rev 53: 948–1017.
- 9. Zotterman Y (1936) Specific action potentials in the lingual nerve of cat. Skand Arch Physiol 75: 105–119.
- 10. McKemy DD, Neuhausser WM, Julius D (2002) Identification of a cold receptor reveals a general role for TRP channels in thermosensation. Nature 416: 52–58.
- 11. Okazawa M, Takao K, Hori A, Shiraki T, Matsumura K, et al. (2002) Ionic basis of cold receptors acting as thermostats. J Neurosci 22: 3994–4001.
- 12. Abe J, Hosokawa H, Sawada Y, Matsumura K, Kobayashi S (2006) Ca2+-dependent PKC activation mediates menthol-induced desensitization of transient receptor potential M8. Neurosci Lett 397: 140–144.
- 13. Dhaka A, Viswanath V, Patapoutian A (2006) Trp ion channels and temperature sensation. Annu Rev Neurosci 29: 135–161.
- 14. Peier AM, Moqrich A, Hergarden AC, Reeve AJ, Andersson DA, et al. (2002) A TRP channel that senses cold stimuli and menthol. Cell 108: 705–715.
- 15. Nakayama T, Hardy JD, Eisenman JS (1961) Single Unit Activity of Anterior Hypothalamus during Local Heating. Science 134: 560–&.
- 16. Kobayashi S (1989) Temperature-sensitive neurons in the hypothalamus: a new hypothesis that they act as thermostats, not as transducers. Prog Neurobiol 32: 103–135.
- 17. Bautista DM, Siemens J, Glazer JM, Tsuruda PR, Basbaum AI, et al. (2007) The menthol receptor TRPM8 is the principal detector of environmental cold. Nature 448: 204–208.
- 18. Takashima Y, Daniels RL, Knowlton W, Teng J, Liman ER, et al. (2007) Diversity in the neural circuitry of cold sensing revealed by genetic axonal labeling of transient receptor potential melastatin 8 neurons. J Neurosci 27: 14147–14157.
- 19. Dhaka A, Earley TJ, Watson J, Patapoutian A (2008) Visualizing cold spots: TRPM8-expressing sensory neurons and their projections. J Neurosci 28: 566–575.
- 20. Abe J, Hosokawa H, Okazawa M, Kandachi M, Sawada Y, et al. (2005) TRPM8 protein localization in trigeminal ganglion and taste papillae. Brain Res Mol Brain Res 136: 91–98.
- 21. Dhaka A, Murray AN, Mathur J, Earley TJ, Petrus MJ, et al. (2007) TRPM8 Is Required for Cold Sensation in Mice. Neuron 54: 371–378.
- 22. Colburn RW, Lubin ML, Stone DJ Jr, Wang Y, Lawrence D, et al. (2007) Attenuated Cold Sensitivity in TRPM8 Null Mice. Neuron 54: 379–386.
- 23. Tajino K, Matsumura K, Kosada K, Shibakusa T, Inoue K, et al. (2007) Application of menthol to the skin of whole trunk in mice induces autonomic and behavioral heat-gain responses. Am J Physiol Regul Integr Comp Physiol 293: R2128–2135.
- 24. Almeida MC, Steiner AA, Branco LG, Romanovsky AA (2006) Cold-seeking behavior as a thermoregulatory strategy in systemic inflammation. Eur J Neurosci 23: 3359–3367.
- 25. Karashima Y, Damann N, Prenen J, Talavera K, Segal A, et al. (2007) Bimodal action of menthol on the transient receptor potential channel TRPA1. J Neurosci 27: 9874–9884.
- 26. Xiao B, Dubin AE, Bursulaya B, Viswanath V, Jegla TJ, et al. (2008) Identification of transmembrane domain 5 as a critical molecular determinant of menthol sensitivity in mammalian TRPA1 channels. J Neurosci 28: 9640–9651.
- 27. Sherkheli MA, Vogt-Eisele AK, Bura D, Marques LRB, Gisselmann G, et al. (2010) Characterization of Selective TRPM8 Ligands and their Structure Activity Response (SAR) Relationship. Journal of Pharmacy and Pharmaceutical Sciences 13: 242–253.
- 28. Kwan KY, Allchorne AJ, Vollrath MA, Christensen AP, Zhang DS, et al. (2006) TRPA1 contributes to cold, mechanical, and chemical nociception but is not essential for hair-cell transduction. Neuron 50: 277–289.
- 29. Nakamura K, Morrison SF (2007) Central efferent pathways mediating skin cooling-evoked sympathetic thermogenesis in brown adipose tissue. Am J Physiol Regul Integr Comp Physiol 292: R127–136.
- 30. Nakamura K, Morrison SF (2008) A thermosensory pathway that controls body temperature. Nat Neurosci 11: 62–71.
- 31. Rim JS, Xue B, Gawronska-Kozak B, Kozak LP (2004) Sequestration of thermogenic transcription factors in the cytoplasm during development of brown adipose tissue. J Biol Chem 279: 25916–25926.
- 32. Gonzalez RR, Kluger MJ, Hardy JD (1971) Partitional calorimetry of the New Zealand white rabbit at temperatures 5-35 degrees C. J Appl Physiol 31: 728–734.
- 33. Penfield W, Rasmussen T (1950) The cerebral cortex of man. A clinical study of localization of function. New York: Macmillan.
- 34. Mazzarello P (1999) A unifying concept: the history of cell theory. Nature Cell Biology 1: E13–E15.
- 35. Alberts B, Johnson A, Lewis J, Raff M, Roberts K, et al. (2008) Molecular biology of the cell. New York: Garland Science.
- 36. Green BG (1992) The Sensory Effects of L-Menthol on Human Skin. Somatosensory and Motor Research 9: 235–244.
- 37. Green BG, Schoen KL (2007) Thermal and nociceptive sensations from menthol and their suppression by dynamic contact. Behav Brain Res 176: 284–291.
- 38. Chuang HH, Neuhausser WM, Julius D (2004) The super-cooling agent icilin reveals a mechanism of coincidence detection by a temperature-sensitive TRP channel. Neuron 43: 859–869.
- 39. Zhang J, Kaasik K, Blackburn MR, Lee CC (2006) Constant darkness is a circadian metabolic signal in mammals. Nature 439: 340–343.
- 40. Sawada Y, Hosokawa H, Hori A, Matsumura K, Kobayashi S (2007) Cold sensitivity of recombinant TRPA1 channels. Brain Res 1160: 39–46.
- 41. Cannon B, Nedergaard J (2004) Brown adipose tissue: function and physiological significance. Physiol Rev 84: 277–359.