Homeotherms have specific mechanisms to maintain a constant core body temperature despite changes in thermal environment, food supply, and metabolic demand. Brown adipose tissue, the principal thermogenic organ, quickly and efficiently increases heat production by dissipating the mitochondrial proton motive force. It has been suggested that activation of brown fat, via either environmental (i.e. cold exposure) or pharmacologic means, could be used to increase metabolic rate and thus reduce body weight. Here we assess the effects of intermittent cold exposure (4°C for one to eight hours three times a week) on C57BL/6J mice fed a high fat diet. Cold exposure increased metabolic rate approximately two-fold during the challenge and activated brown fat. In response, food intake increased to compensate fully for the increased energy expenditure; thus, the mice showed no reduction in body weight or adiposity. Despite the unchanged adiposity, the cold-treated mice showed transient improvements in glucose homeostasis. Administration of the cannabinoid receptor-1 inverse agonist AM251 caused weight loss and improvements in glucose homeostasis, but showed no further improvements when combined with cold exposure. These data suggest that intermittent cold exposure causes transient, meaningful improvements in glucose homeostasis, but without synergy when combined with AM251. Since energy expenditure is significantly increased during cold exposure, a drug that dissociates food intake from metabolic demand during cold exposure may achieve weight loss and further metabolic improvements.
Citation: Ravussin Y, Xiao C, Gavrilova O, Reitman ML (2014) Effect of Intermittent Cold Exposure on Brown Fat Activation, Obesity, and Energy Homeostasis in Mice. PLoS ONE 9(1): e85876. https://doi.org/10.1371/journal.pone.0085876
Editor: Marcia B. Aguila, State University of Rio de Janeiro, Biomedical Center, Institute of Biology, Brazil
Received: September 10, 2013; Accepted: December 3, 2013; Published: January 17, 2014
This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Funding: This research was supported by the Intramural Research Program (ZIA DK075062, ZIA DK075064, ZIA DK070002) of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH. YR was supported by a grant from the Swiss National Fund for Scientific Research (SNF). 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.
Cold exposure in mammals elicits behavioral and physiological responses that minimize heat dissipation (e.g. vasoconstriction, huddling) and increase heat generation (e.g. shivering, activation of brown adipose tissue [BAT]) . The demonstration that adult humans have functional and inducible brown adipocytes – caused a resurgence of interest in BAT regulation and the effects of cold exposure on metabolism and metabolic regulation. In addition, inducible forms of BAT (termed beige or brite adipose tissue) arising within white adipose tissue and with distinct developmental lineages were recently identified . These discoveries have led to the notion that simply increasing BAT quantity and/or function may reduce body weight by dissipating excess calories –. Transgenic , BAT transplantation , and β3-adrenergic agonist  murine studies support this claim, yet these experiments all cause supra-physiologically elevated levels of uncoupling protein 1 (Ucp1) and/or BAT mass. β3-adrenergic agonist stimulation in dogs, mice and rats can cause significant reductions in adiposity . Yet all of the above approaches are non-physiological manipulations that bypass counter-regulatory adaptations that are likely activated during normal cold-induced UCP1 up-regulation . Continuous cold exposure experiments in rodents have yielded conflicting results, with some studies showing decreased weight gain in rats exposed to cold ,  and others showing no alteration in body weight .
Inspired by the beneficial effects of exercise, an intrinsically intermittent process, we explore the effects of intermittent cold exposure. Intermittent cold exposure experiments have been conducted in rodents but many of these experiments assessed the changes in cold tolerance, heat loss parameters , , and feeding behavior, not specifically whether cold ameliorates the negative health consequences of the obese state. Whether increases in the endogenous activation of BAT via environmental stimuli (e.g. cold exposure) can cause metabolic improvements in a diet-induced obese (DIO) murine model is not known.
Modulating ambient temperature in order to affect metabolism is an attractive idea that has recently gained traction. It has been suggested that cooler temperatures in human living spaces could reduce body weight and ameliorate comorbidities of obesity  by increasing the amount and/or activity of BAT. The goal of the present study was to assess the metabolic effects of intermittent cold exposure in DIO C57BL/6J mice.
Materials and Methods
Animals and diet
Fourteen-week-old DIO C57BL/6J male mice that had been fed a high-fat diet starting at 6 weeks of age (D12492, 60% kcal fat, 5.24 metabolizeable kcal/g; Research Diets, New Brunswick, NJ) were purchased from Jackson Laboratory (Bar Harbor, ME). At NIH, animals were individually housed at 22–24°C with a 12∶12-h dark-light cycle (lights on at 0600h) in a clean, conventional facility in plastic pens with wood-chip bedding and ad-libitum access to D12492 diet and water. The protocol was approved by the NIDDK Institutional Animal Care and Use Committee.
ICE#1 and ICE#2.
Following a 4-week acclimatization period, the mice were ranked by weight and distributed into three groups (8 mice/group) of equal mean body weight. On days of cold exposure (Monday, Wednesday, Friday), body weight and food intake were measured and cages were transferred to a 4°C room for the indicated number of hours (intermittent cold exposure: ICE). Control mice were similarly moved to a new room at 22°C for 1 hour (ICE#1) or 4 hours (ICE#2). Body composition (fat mass and fat-free mass) was measured by time domain Echo MRI 3-in-1 (Echo Medical Systems, Houston, TX) every 2 weeks in early morning.
Following a 4-week acclimatization period, the mice were ranked by weight and distributed into four groups (6 mice/group) of equal mean body weight. Two groups were exposed to 4°C for 4 hours three times per week while 2 control groups were treated similarly at 22°C (control: CON). Mice were treated daily with either vehicle or AM251 (3 mg/kg in 5% DMSO/5% Tween 80 in saline; Cayman Chemical, Ann Arbor, MI) by oral gavage. Body weight and food intake were measured daily prior to gavage.
At the end of the studies, mice were administered ketamine (100 mg/kg) and xylazine (10 mg/kg) by ip injection, blood was obtained by retro-orbital bleed, and tissues were removed, weighed, and frozen at −80°C until assayed.
Total energy expenditure
Average total energy expenditure (TEE) was calculated using the energy balance technique (caloric intake minus change in body energy stores) . In brief, the body composition caloric equivalents (fat mass, 9.4 kcal/g; fat-free mass, 1.0 kcal/g) are used to correct for body composition changes. The increase in body kcal content is subtracted from the total metabolizeable energy intake, yielding the TEE, which is divided by the experiment duration (ICE#1 – 77 days; ICE#2 – 74 days; ICE#3 – 28 days) to give the average daily TEE.
CL316243, a selective β3-adrenoceptor agonist was used to maximally stimulate facultative thermogenesis during indirect calorimetry . These experiments were performed at thermoneutrality (30°C) to eliminate endogenous BAT activation. Mice were placed in a 12-chamber Environment Controlled CLAMS (Columbus Instruments, Columbus, OH) early in the morning (0645h), acclimatized for ∼4 hours, treated with CL316243 (100 µg/kg in saline, ip), and energy expenditure was measured for 5 more hours. Mice had ad libitum access to food and water during the entire testing period.
Intra-peritoneal glucose tolerance test (ipGTT)
Mice were fasted overnight, glucose (1 g/kg body weight, ip) injected at 0900h, and tail blood glucose measured (Glucometer Contour, Bayer, Mishawaka, IN) at 0, 15, 30, 60, and 120 minutes post-injection. The ipGTT was conducted one day following cold exposure in ICE#1 and ICE#3 and two days after cold exposure in ICE#2 to probe the duration of cold exposure's effects. In ICE#2, insulin concentrations were also determined at 0, 15, and 120 minutes by RIA (Millipore, St. Charles, MO).
Insulin tolerance test (ITT)
Non-fasted mice were injected with 0.75 U/kg body weight insulin (Humulin, Eli Lilly, Indianapolis, IN) at 0900h. Tail blood glucose concentrations were measured at 0, 15, 30, 45, 60, and 120 minutes post-injection.
In ICE#1, in vivo glucose uptake was measured by ip injection of [1-14C]2-deoxyglucose (10 µCi, Perkin Elmer, Boston MA) one hour prior to termination of mice. Mice were injected at initiation of cold exposure in the 1 h group and 3 hours after the start of the cold exposure in the 4 h group. Sixty minutes post injection, two muscles (quadriceps and gastrocnemius), two fat pads (inguinal and epididymal), interscapular BAT, and the spleen were removed, weighed, homogenized, and the [14C]2-deoxyglucose 6-phosphate was extracted using Poly-Prep Prefilled Chromatography Columns (Bio-Rad Laboratories, Cat: 731-6211, Hercules, CA) and quantitated using Beckman Liquid Scintillation Counter .
Serum hormone and metabolite profiles
Blood from retro-orbital bleeding was put in BD Microtainer Serum Separator Tubes (Becton, Dickinson and Company, Franklin Lakes, NJ), allowed to clot for 10 minutes at room temperature, spun at 10,000 rpm for 6 minutes, and serum was frozen until assayed. Free fatty acids (Roche Diagnostics Gmbh, Mannheim, Germany), triglycerides (Pointe Scientific Inc., Canton, MI), cholesterol (Thermo Scientific, Middletown, VA), β-hydroxybutyrate (BioVision, Milpitas, CA), and D-lactate (BioVision, Milpitas, CA) were measured by colorimetric assays. Serum glucose was measured by Glucometer Contour. Insulin (Millipore, St. Charles, MO), adiponectin (Millipore, St. Charles, MO), insulin-like growth factor 1 (ALPCO, Salem, NH), T3 (DiaSorin Inc, Stillwater, MN), and T4 (DiaSorin Inc, Stillwater, MN) were measured by RIA. Leptin (R&D Systems, Minneapolis, MN) and fibroblast growth factor 21 (Millipore, St. Charles, MO) were measured by ELISA. All assays were conducted as per manufacturer's protocol.
Gene expression analyses
RNA was extracted (Qiagen RNeasy Plus Mini Kit, Germantown, MD), converted to cDNA (Roche Transcriptor High Fidelity cDNA Synthesis Kit, Indianapolis, IN), and quantitated by real-time polymerase chain reaction (qRT-PCR, Applied Biosystems 7900HT, Foster City, CA). Both SYBR green-based and taqman primer probe systems were used.
Data are expressed as group mean ±SE. Statistical analyses were performed using JMP (version 9; SAS, North Carolina). For ICE#1 and ICE#2, one-way ANOVAs were conducted using mouse group as independent variables (CON, 1 h, 4 h for ICE#1 and CON, 4 h, 8 h for ICE#2). For ICE#3, two-way ANOVAs used cold exposure (ICE or CON) and drug treatment (AM or VEH) as grouping variables. For significant ANOVA results, a Tukey HSD post-hoc test was conducted to compare among groups. Statistical significance was prospectively defined as P<0.05.
Cold exposure increases energy expenditure and food intake, without altering body weight
Two independent experiments, exposing mice to 4°C for 0, 1, or 4 hours (ICE#1) or 0, 4, or 8 hours (ICE#2) three times a week for ∼10 weeks, are presented together but were performed sequentially. This design tests a range of cold exposure durations and allows sufficient time so that metabolic and physiologic changes in the mice are likely in a new steady state. Food intake was increased in the cold exposed groups in a dose-dependent manner (Figure 1A). However, body weight was not affected by intermittent cold exposure (Figure 1B). Similarly, no consistent differences were observed in fat mass, fat-free mass, inguinal WAT, epididymal WAT, interscapular BAT, or liver weights (Tables 1, 2). TEE over the ∼10 weeks was calculated from the caloric intake corrected for changes in body composition . Cold exposure of 1 and 4 hours increased TEE by 4.5% and 7.2%, respectively (ICE#1; Table 1) and 4 and 8 hours increased it by 7.6% and 12.2% (ICE#2; Table 2). Assuming that all of the metabolic rate increase occurs during cold exposure, these data indicate an approximate doubling of metabolic rate during the cold challenge. Taken together, these data demonstrate that modest doses of intermittent cold exposure do not alter body weight or adiposity since increases in food intake fully compensate for the cold-induced increases in energy expenditure.
A: Caloric intake and B: body weight during ICE#1 (top) and ICE#2 (bottom) experiments were measured three times per week on days of cold exposure. Timing of the intra-peritoneal glucose tolerance tests (GTT) and CL316243 treatment (CL) are indicated. Data are mean ±SE, N = 8/group. The 8 h group had higher food intake as assessed by repeated measures ANOVA (p<0.05).
BAT activation by cold exposure
As a probe for cold-induced changes in adipose physiology, CL316243, a selective β3-adrenergic receptor agonist, was used to estimate the capacity for heat generation . In the control mice, CL316243 increased TEE by ∼2.5-fold from the thermoneutral baseline (Figure 2). Cold-exposed mice had a greater increase in metabolic rate following injection of CL316243 than controls: 6.5% (not significant) and 19% (p<0.05) greater in the 1 and 4 hour groups, respectively (ICE#1) and 26% (p<0.05) and 29% (p<0.05) greater in the 4 and 8 hour groups, respectively (ICE#2, Figure 2).
In ICE#1 (top) and ICE#2 (bottom), mice were placed in the individual chambers at 30°C at −250 minutes, injected CL316243 (100 µg/kg) at time 0 as described in Experimental Procedures. Energy expenditure was measured every 13 minutes. The initial metabolic rate peak seen in all groups is a stress response caused by handling. Inset shows the delta energy expenditure, calculated as the mean post-CL316243 (minutes 26 to 312) minus the mean pre-CL316243 (minutes −78 to 0) energy expenditure in kcal/h. Data are mean ±SE, N = 8/group. Levels not connected by same letter are significantly different (P<0.05).
To examine the transcriptional response to intermittent cold, markers of BAT activation were studied. Ucp1 mRNA was slightly (∼25%), but not significantly, increased in the 1 h, 4 h, and 8 h groups in ICE#1 and #2 (Tables 1, 2). No significant difference in Ucp1 protein levels was detected (data not shown). Pgc1α, a transcriptional co-activator involved in mitochondrial biogenesis and in the induction of thermogenic genes , was significantly increased in both the 4 h groups (∼4-fold vs. control) and the 8 h group (∼7-fold vs. control) (Tables 1, 2). No histologic differences were observed comparing iBAT from mice in the different treatment groups. These changes are consistent with a moderate increase in BAT activation with cold exposure.
We next investigated if the cold exposure induced beige/brite adipose tissue. As expected, at baseline BAT markers were very low in WAT (BAT: WAT ratios for Ucp1 of ∼4000 and Pgc1α of ∼10). Cold exposure had no consistent effect in the 1 h or 4 h groups, with a possible induction (not statistically significant) in the 8 h group (Tables 1, 2). Likewise, two other beige/brite markers (Cd137 and Tmem26) showed no differences in gene expression (data not shown).
Tissue glucose uptake was measured using 2-deoxyglucose, which probes glucose transport predominantly in the 45 minutes after 2-deoxyglucose injection, weighted to the first minutes after injection due to exponential decay kinetics  (data not shown). In the 1 h cold treatment group with 2-deoxyglucose dosed at the start of the cold exposure, a 2-fold increase in gastrocnemius uptake was observed with no significant increase in BAT or other tissues (Table 3). These results suggest that muscle was a principal glucose-driven thermogenic tissue during this time interval, likely due to shivering. In the 4 h treatment group with 2-deoxyglucose dosed 3 hours after the start of cold exposure, 2-deoxyglucose uptake in BAT increased 39% (non-significant) and decreased in most other tissues (significantly so in quadriceps, iWAT, and spleen; Table 3). These results suggest that BAT thermogenesis was turned on in the 4 h group, with reduced glucose uptake in other tissues, consistent with a ‘steal’ phenomenon in which one tissue's uptake reduces the availability of glucose for uptake by other tissues.
Taken together, these data demonstrate that intermittent cold exposure increases thermogenic capacity, with modest increases in mRNA markers of BAT activation, and no consistent activation of beige/brite adipose tissue.
Cold effect on energy homeostasis
In ICE#1, an ipGTT was conducted the day following cold exposure to examine the effects of cold exposure on glucose tolerance. The 4 h group had decreased glucose concentrations at most time points and a significantly lower area under the curve (AUC) compared to the 1 h group (Figure 3 top). In ICE#2, the ipGTT was performed two days after cold exposure to probe for longer lasting effects. With this paradigm, no significant effect was observed (Figure 3 bottom), suggesting that there is a modest, transient beneficial effect of cold exposure on ipGTT.
In ICE#1 (top) and ICE#2 (bottom), intra-peritoneal glucose tolerance tests (1 g/kg) were performed in the overnight-fasted mice. In ICE#1, the ipGTT was conducted the day after cold exposure, while in ICE#2 it was conducted on the second day following cold exposure. The inset shows the mean area AUC in mg/dl•min ±SE, N = 8/group. Levels not connected by same letter are significantly different (P<0.05).
In serum samples obtained at euthanasia after cold exposure, circulating free fatty acids were increased (Table 1, 2), the result of lipolysis and fatty acid release from WAT. Insulin levels were slightly reduced by cold exposure, likely due to increased glucose utilization. No significant differences were observed in serum glucose, triglyceride, cholesterol, or adiponectin concentrations (Table 1, 2). Regression analysis of leptin level vs. fat mass revealed the expected  positive correlation (data not shown). In addition, leptin concentrations were reduced by acute cold exposure indicating that cold, like fasting , reduces circulating leptin concentrations.
No synergistic effects of cold exposure and AM251 on body weight, body composition, or food intake
Since cold exposure increases food intake, we tried combining cold exposure with an obesity drug that reduces food intake. In ICE#3, we tested, individually and in combination, 4-hour cold exposure and AM251, a cannabinoid receptor 1 (CB1) inverse agonist that both reduces food intake and increases metabolic rate . The AM251 dose (3 mg/kg/day) was chosen as efficacious, but well below maximum efficacy , thereby allowing room in the assay to detect additional weight loss. AM251 caused rapid and sustained weight loss that was similar in the cold exposed (ICE AM, −16±2%, p<0.05) and control (CON AM, −17±2%, p<0.05) groups (Figure 4A and Table 4). Total fat mass and inguinal and epididymal fat pad weights were reduced by ∼30% (P<0.05) in AM251 treated animals (Table 4). Decreased fat mass accounted for nearly all the weight loss in the drug treated animals.
Mice were administered vehicle or AM251 (3 mg/kg/day) by oral gavage. A: Caloric intake and B: body weight were measured three times per week on days of cold exposure. C: Mice at 30°C were administered CL316243 (100 µg/kg) at time 0 as described in Experimental Procedures (the prior AM251 was given at −24 hours). Inset shows the delta TEE, calculated as in Figure 2. 2-way ANOVA showed significant temperature (p<0.01) and drug (p<0.05) effects with no significant interaction (p = 0.62). D: Intra-peritoneal glucose tolerance tests (1 g/kg) were performed in overnight-fasted mice of the indicated treatment group two days after cold exposure. AUC numbers are in mg/dl•minute. E. Insulin tolerance test. Insulin (0.75 U/kg) was injected and blood glucose measured at the indicated times. GTT = intraperitoneal glucose tolerance test. CL = CL316243 experiment. ITT = insulin tolerance test. AM251 was administered 24 h prior to the GTT and ITT. In D & E, a poor-responding outlier in the CON AM group was removed from the analysis. If included in the ipGTT AUC, this group's AUC is 29304 ±3382 mg/dl min and the CON AM significantly different from the ICE AM group. All data are mean ±SE. N = 6/group. Levels not connected by same letter are significantly different (P<0.05).
As expected, cumulative food intake was significantly decreased by AM251 in CON mice. AM251 also decreased food intake in cold exposed mice, but did not inhibit the compensatory increase in food intake caused by the elevated TEE of cold exposure (Figure 4B). 2-way ANOVA analysis of TEE revealed that cold exposure significantly increased TEE but AM251 did not (Table 4). Thus, there is no evidence for augmented (or reduced) benefits from combining cold exposure and AM251 on body weight, fat mass, or food intake.
AM251 decreases CL316243-induced energy expenditure but does not affect BAT specific markers
AM251 is reported to cause weight loss partially through up-regulation of Ucp1 in BAT . However, in AM251-treated mice, CL316243-induced energy expenditure was reduced compared to controls (Figure 4C). The decreased response to CL316243 is likely due to less lipolysis from the reduced fat mass of the AM251-treated animals. Gene expression of both Pgc1α and Ucp1 in BAT showed no significant differences among the groups. Analysis by ANOVA revealed a significant effect of prior cold exposure to increase (p<0.05) and of AM251 treatment to decrease (p<0.05) CL316243-stimulated energy expenditure, but no interaction (p = 0.63) (Figure 4C).
Combined effect of AM251 and cold on glucose and insulin tolerance
AM251 improves impaired glucose homeostasis , but how a combination of intermittent cold and AM251 administration affects such parameters is not known. ipGTT and ITT were performed two days after cold exposure, as in ICE#2 to probe for a durable effect. Glucose tolerance was significantly improved in the ICE AM and CON AM groups at the 30- and 60-minute time points compared to the ICE VEH group (Figure 4D). 2-way ANOVA using drug (±AM251) and cold exposure (±ICE) as independent variables and the AUC as the dependent variable, revealed a significant drug effect (p = 0.035) but no cold effect or interaction. Non-fasting serum glucose concentrations were significantly lower in the ICE AM compared to other groups at the beginning of the ITT (Figure 4E). Although CON AM serum glucose concentrations started significantly higher than ICE AM, they reached nearly identical concentrations 30 minutes following insulin injection (96.4±5.0 vs. 93.5±5.4 mg/dl respectively). Taken together, these data demonstrate that AM251 significantly decreases body weight and fat mass with beneficial effects on ipGTT and ITT but no clear synergistic effects when combined with cold exposure.
Effect of AM251 and cold exposure on hormones and metabolites
In ICE#3, the mice were not exposed to cold at the terminal sampling, unlike ICE#1 and ICE#2, allowing differentiation between acute and more persistent effects of cold exposure. Circulating free fatty acid and triglyceride concentrations were significantly lower in ICE vs. CON mice irrespective of drug treatment (Table 4). β-hydroxybutyrate and D-lactate concentrations were lower in both ICE AM and ICE VEH when compared to CON AM but not CON VEH. Insulin was slightly but not significantly elevated in the two ICE groups compared to CON mice. No significant differences were observed in serum glucose, cholesterol, adiponectin, leptin, T3, FGF-21, or IGF-1 when compared with CON mice.
We have investigated the metabolic and physiologic consequences of moderate doses of intermittent cold exposure in DIO mice. Cold exposure increases food intake, energy expenditure, thermogenic capacity, and expression of BAT activation genes. Despite activation of BAT, there were no changes in body weight or composition, yet there were transient improvements in glucose homeostasis.
In our experiments, the acute cold-induced increase in energy expenditure is large (∼2 fold), but the overall increase in daily TEE is modest (4–12%). The appearance of brown adipocytes in typically white adipose depots occurs with prolonged exposure to cold temperatures , . The current study produced only mild changes in interscapular BAT and no browning of the inguinal fat pad, results that are consistent with the modest level of additional cold challenge. Three questions are highlighted by our observations.
How does intermittent BAT activation compare to exercise?
Initiating low levels of exercise in sedentary rats slightly reduced body weight and food intake. With higher exercise levels, weight remained stable while food intake rose, nearly doubling . Like the sedentary state, mice housed at thermoneutrality are heavier than those housed at room temperature –, supporting the parallel between muscle exercise and BAT activation. In our experiments, the control mice were housed at 22°C, below the thermoneutral zone, so the additional cold exposure is analogous to increasing exercise in mice that are already getting some exercise. It is plausible that intermittent cold exposure in mice otherwise housed at thermoneutrality would produce a body weight reduction.
In DIO mice, exercise protected against weight gain despite increased food intake, reduced adipose tissue inflammation, and improved insulin sensitivity . Human epidemiologic evidence suggests that exercise training in obese patients improves glucose control and reduces inflammation, independent of weight loss . It is unknown if cold-induced BAT activation would do the same, either by a non-specific increase in metabolic demand, or via specific BAT hormones, analogous to irisin from muscle  or leptin and adiponectin from adipose tissue. However, the observation of transiently improved glucose tolerance is an encouraging sign. The improvement in insulin sensitivity with exercise in the absence of weight loss occurs in muscle ; whether the improvement with cold exposure occurs directly in BAT is not known.
Cold exposure will always increase metabolism, whether via BAT activation or shivering . BAT is efficient in generating heat via dissipating the proton motive force. Shivering involves the work of muscle contraction, so some of the energy is used for force production and this physical work/kinetic energy reduces the fraction of energy spent on heat production .
Is BAT activation per se expected to reduce body weight?
Prior experiments suggest that increases in BAT quantity and/or activation can cause weight loss. Examples include BAT activation by transgenic manipulation , BAT transplantation , and β3-adrenergic agonist treatment –. The effect of BAT activation depends on whether the activation increases energy expenditure beyond the endogenous level, either by large increases in thermogenesis, or by affecting regulatory mechanisms. Long term increased energy expenditure is expected to be balanced by increased food intake to avoid eventual starvation. Indeed, in one study using CL316243, an initial reduction in food intake was followed by an increase over baseline . Studies using chronic β3-adrenergic agonist treatment typically find little (or transient) weight loss and an increase in food intake , –. The protection of body weight is not limited to β3-adrenergic agonist stimulation or modest doses of cold—mice chronically exposed to −3°C maintain their body weight despite a 4-fold increase in metabolic rate . In summary, achieving weight loss depends on how food intake compensates for the increase in energy expenditure, so BAT activation per se is not sufficient for weight loss.
Are there strategies for using modest cold exposure that would ameliorate obesity and its metabolic consequences?
Successful therapeutic use of cold exposure requires blunting the accompanying increase in food intake. To address this issue, we investigated combining cold exposure with a weight loss drug, AM251, a cannabinoid receptor inverse agonist that reduces food intake. However, while both cold and AM251 maintained their individual effects, the combination did not yield augmented benefit. Another possible approach would be to supplement leptin levels. Cold stress induces central nervous system leptin receptor gene expression  and decreases WAT leptin . Leptin replacement to the levels present in the absence of cold exposure would address this idea.
Is the mouse a relevant model for human energy homeostasis? Due to their large surface area-to-volume ratio, small mammals are exquisitely sensitive to environmental temperature and capable of drastically increasing BAT thermogenesis and food intake in response to decreases in ambient temperature. While it has been known since Lavoisier (ca 1790) that food intake and metabolic rate are increased by cold in humans , only relatively recently was it established that BAT is contributing to the cold-induced increase in thermogenesis in adult humans. Thus, while the magnitude of the effect is dramatically different, the biological insights from the mouse should provide fruitful investigative paths vis-à-vis BAT activation and function in humans. For example one of two recent human cold exposure trials did observe a reduction in fat mass , .
In summary, modest intermittent cold exposure does not reduce body weight or fat mass in mice but appears to transiently improve glucose homeostasis. The stimulation of BAT by cold has similarities to the stimulation of muscle by physical activity. Reducing the compensatory increase in food intake seen with cold exposure would be an effective way to achieve weight loss and improve metabolic status. Devising optimal use of cold exposure requires understanding how to combine it with exercise, food restriction, and pharmacologic therapy.
We thank Tatyana Chanturiya, Margalit Goldgof, William Jou, Dalya Lateef, and Cecelia Nigro for excellent technical assistance and advice.
Conceived and designed the experiments: YR OG MLR. Performed the experiments: YR CX OG. Analyzed the data: YR CX OG MLR. Wrote the paper: YR MLR.
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