Lose weight Without Exercising or Making Any Dietary Change?

Tackling obesity without exercise or dietary changes? Everyone’s heard of fat tissue (also called adipose tissue), but what about brown adipose tissue (BAT) and “beige” adipose tissue – ever heard of them? Although sounding pretty unappetising,  these adipocytes1 share the unique ability of being able to convert chemical energy into heat and, thereby, play a critical role in promoting something called non-shivering thermogenesis – a little-known process that is central to the human species’ ability to spread across the globe and, as an interesting sideline, can potentially help in weight-loss without even having to lift a single barbell or place a tentative trainer on that running machine gathering dust in your garage. Or is it just too good to be true?

BAT & beige adipocytes

Until relatively recently, the physiological role of BAT and beige adipocyte depots were thought to be limited to small mammals and only relevant to humans when they were neonates (newborn infants). Puppy fat or baby fat was thought to all-but disappear with the passing years into adulthood. However, the discovery that there’s more BAT in adult humans than previously thought, has led to studies which show enthusiasm for BAT’s potential role in treating obesity and other disorders caused by sustained positive energy balance (more calories in than out). Adult humans having more BAT than previously thought was revealed 2 3 during routine scans  (FDG-PET scans4 to detect metastatic cancers. 5  Autopsies were also able to reveal these fat concentrations. 6

Brown & white fat

BAT (often abbreviated to “brown fat”) is found in virtually all mammals, but notably in newborn humans and mammals that hibernate 7 . Of course, the usual white adipose tissue (“white fat”) that we think of when we talk about fat is found in far higher quantities. 8 . The following provides an overview of the differences between the brown and white fat tissue:

The main differences between brown and white fat can be summarised as:

  • white contains a single lipid droplet while brown contains numerous smaller droplets
  • brown contains a much much higher number of (iron-containing) mitochondria – hence the brown (rusty) colour of the tissue 9
  • brown contains more blood capillaries than white – hence a better oxygen supply, more nutrient-provision and the ability to distribute the produced heat throughout the body

Two types of BAT

BAT itself can also broken down into two types which have similar functions but are located in different cell populations within the body: 10

  • brown adipocytes found in comparatively larger separate deposits within the body, and
  • “beige” or “brite” (“brown in white”) adipocytes found interspersed within white adipose tissue and which develop out of white adipocytes under the stimulation of the sympathetic nervous system (SNS) 11
Brown adipose tissue in a woman shown in a PET/CT scan exam.

BAT in infants & adults

BAT in infants eventually “turns into” white fat in adulthood. In infancy, however, it tends to be located in the following “depots” within the body:

  • interscapular 12
  • supraclavicular 13
  • suprarenal 14
  • pericardial 15
  • paraaortic 16
  • around the pancreas, kidney and trachea 17

BAT in adults tend to be located in the following depots:

  • supraclavicular
  • suprarenal
  • paravertebral 18
  • mediastinal 19
  • paraaortic 20

It’s still not absolutely clear whether these adult BAT depots are the “classical” brown or the beige/brite fat. 21 . However, BAT is metabolically active in adult humans 22  and decreases in quantity as we age 23 . Another characteristic of BAT is that it becomes more visible (that is, becomes more metabolically active) with cold exposure – as can be seen by analysing it with PET scans.

BAT & thermoregulation

The primary function of BAT is thermoregulation. That is, ensuring the body remains sufficiently warm in cold environments. It achieves this autonomic heating of the body in two ways: firstly, through shivering thermogenesis (causing muscles to shiver) and, secondly, through non-shivering thermogenesis (as the name suggests – heating the body without shivering) – an adaptive thermogenesis response. The first option, shivering thermogenesis, will certainly warm up the body, but at the expense of using up relatively more precious energy.

However, the unique ability of BAT to convert energy stores (brown fat) into heat (without needing to use energy-sapping shivering) is achieved through a process within BAT mitochondria (the energy-producing cellular power plants). Instead of the usual process, where ATP (the energy molecule) is produced during oxidative phosphorylation, a protein called thermogenin or UCP1 (Uncoupling Protein 1) promotes a proton leak in the inner membrane of the mitochondria, dissociating the oxidative phosphorylation of substrate from the generation of ATP. In essence, this results in an increase in non-shivering thermogenesis, where the metabolic rate increases, and chemical energy is shunted into heat energy that can then spread around the body via the bloodstream.

This means the endothermic organisms (you and me) stand a better chance of survival against unfavourable environmental conditions with the least possible consumption of energy stores 24 . This can be seen in a little more clearly in the following diagram:

Just to be clear, all cells of endotherms are able to give off heat to some degree, particularly when body temperature is below a regulatory threshold; but BAT is highly specialised for this non-shivering thermogenesis. This is largely because of two of the features mentioned above: firstly, each BAT cell has a higher number of mitochondria compared to typical cells and, secondly, these mitochondria have a higher-than-normal concentration of thermogenin (UCP1) in the inner membrane.

Why do newborns have so much BAT?

In newborn infants, BAT comprises around 5% of body mass (located on the upper half of the spine and toward the shoulders). At this age, infants are at a much higher risk of hypothermia than adults. This is largely because of the following:

Infants have:

  • underdeveloped nervous systems that don’t respond quickly and/or appropriately to cold via vasoconstriction (the contraction of blood vessels in and just below the skin)
  • inability to move away from cold materials or air currents or towards warmer materials/environments
  • low amount of musculature and an inability to shiver (shivering thermogenesis)
  • lack of thermal insulation such as subcutaneous fat and fine body hair
  • higher ratio of body surface area (proportional to heat loss) to body volume (proportional to heat production)
  • higher proportional surface area of the head
  • the obvious inability to use adult ways of keeping warm – putting clothes on, exercising, drying their skin, etc

Thus, heat production in BAT provides infants with an alternative means of heat regulation.

Evolutionary advantage of BAT

Mammals (and birds, to some extent) have the unique ability to maintain their core temperature independently of the external environmental temperature. This homeothermic 25 ability has allowed great evolutionary success compared to poikilotherms2627

The main components of this response to temperature are:

  • thermal insulation
  • non-shivering thermogenesis, and
  • shivering thermogenesis 28

From an evolutionary point of view, excess energy expenditure aimed at maintaining core temperature represents a trade-off between survival and the maintenance of energy stores, since energy availability will usually represent a major limiting factor to growth and reproduction. Thus, moving from an insulative response (energy neutral), to a non-shivering and eventually shivering thermogenesis will require a progressively greater dissipation of energy stores, as can be seen in the following chart.

Model of adaptive thermogenesis. As the environmental temperature decreases from thermoneutrality, the adaptive thermogenesis response moves from insulative to non-shivering and eventually shivering thermogenesis. This progression is mirrored by an increase in the energy expenditure required to maintain the core temperature. Green, energy expenditure due to basal metabolic rate; red, expenditure due to adaptive thermogenesis.

Over recent evolutionary development, humans gained the ability to “control” their environment by using clothes and controlling the temperature in their buildings. As a result, cold exposure is a relatively rare condition and, unless acclimatised, individuals would tend to respond by shivering thermogenesis – where heat is a side product of uncontrolled shivering – also known as muscle fasciculation 29

Losing weight & improving health with BAT

Recent discoveries regarding BAT may, it’s claimed, lead to new methods of weight loss, since brown fat (when exposed to cold temperatures) takes calories from normal fat and burns it. As well as this, adaptive (non-shivering) thermogenesis also appears to promote glucose disposal. To test this weight-loss ability of BAT, it would involve exposing subjects to cold temperatures and monitoring whether they do, in fact, lose weight without having to exercise or change dietary patterns. The following is a selection of some BAT studies that throw some light on this subject.

A 1961 study 30 when individuals had prolonged exposure to cold, showed that they became resilient and stopped displaying shivering thermogenesis, indicating that other mechanisms were being recruited.

In 2009, four separate studies 31 32 33 34 indicated clearly that BAT was present in a significant number of adults and that there was a correlation between its presence and activity related to indices of healthy metabolism.

In 2010, a study 35 showed that there was an inverse correlation between BAT activity and between obesity, diabetes and ageing – that is, the more active BAT was, the less obesity, diabetes and ageing was seen.

Naturally, up to this point, the relationship was one of correlation and no causal mechanism had been established. However, researchers were very interested in finding out more about the capacity and activity of human BAT as a therapeutic means of treating the various metabolic consequences of obesity. The majority of the consequent studies focused on this BAT adaptive thermogenesis response by exposing volunteers to cold.

A 2011 study 36 exposed individuals to short but intense cold (e.g. immersing a limb in ice-cold water). Whilst they showed that this does indeed increase energy expenditure, it’s a method that fails completely to correspond with day-to-day experience and is impossible to sustain over time.

Additional research demonstrated that such extreme cold exposure was not necessary to stimulate sustained physiologic adaptive thermogenesis. It could be stimulated by even mild cold exposure as that controlled within normal (and bearable) climate-controlled buildings. This was shown in a 2010 crossover study 37 which looked at the effects of the adaptive thermogenesis response to minimal changes in environmental temperature. Healthy volunteers underwent two 12-hour periods in a whole room calorimeter (Metabolic Chamber) at 19 and 24 °c to monitor energy expenditure (EE). Results indicated that such minimal modulation of environmental temperature was sufficient to increase EE by around 6%. Might not seem much but, if projected over a 24 hour period, it would represent a drop of 100 kcal in an individual of between 70-80 kg.

Hormonal axes and organ-system response to mild cold exposure.

In addition to burning extra calories, exposure to mild cold (with the resulting increase in non-shivering thermogenesis) was shown to be sufficient to drive an adrenergic response 38 , which promotes lipolysis39 (with fatty acids being the preferred substrate in BAT depots) and increased postprandial glucose disposal. Additionally, the intervention generated an increase in cortisol 40  and a state of relative insulin resistance during fasting, which indicate an activation of the stress response. These, and other responses are shown in the adjacent table.

The researchers point out that, although the magnitude of this change may appear insignificant – only one fifth of the negative energy balance recommended to achieve sustained weight loss – it is relevant to note that, over a 1-year period (all things being equal), these differences would be equivalent to a 20-day fast and to a daily 30-min walk at a moderate pace.

A subsequent 2013 study 41 confirmed BAT contributes to energy expenditure (EE) in response to mild cold exposure – namely, 12-hour metabolic chamber exposure to either 19 or 24 ° C.

Two other 2013 studies showed, in the first case 42 , that a short-term, moderate (10 days acclimatisation with exposure at 17 ° C daily for 2 hours) cold exposure was sufficient to increase the quantity of BAT, and, in the second case 43 , that a longer period of time (6 weeks acclimatisation with exposure at 17 ° C daily for 2 hours) resulted in “significant fat mass reduction“- as shown in the following photos and chart:

BAT activation was shown to improve glucose homeostasis 44 and insulin sensitivity 45 in humans. Additional studies 46 47 looked at BAT and the hormone FGF-21 (fibroblast growth factor 21 production). FGF-21 is a critical metabolic regulator that governs glucose and lipid (fat) metabolism and plays an important role in the treatment of metabolic diseases, such as T2D (type 2 diabetes) and obesity. In T1D (type 1 diabetes), FGF-21 also reduces blood glucose levels and prevents diabetic complications.  It was demonstrated that BAT activation through cold exposure can up-regulate circulating FGF-21 in humans by 37%. FGF21 improves insulin sensitivity and glucose metabolism which may partially explain its longevity promoting benefits.

This offers hope for those with impaired insulin function who might benefit from BAT activation. And it’s not just those with clinically impaired insulin function, such as type 2 diabetics, who could benefit from this. Over time, even mildly elevated blood glucose levels in otherwise healthy non-diabetic humans are associated with other physiological damage. This has been shown to result in higher levels of the damaging AGE’s (advanced glycation end products – found in animal products, processed and fried/barbecued/roasted fatty foods), as well as damage to the brain, eyes, tendons, endothelial cells and the cardiovascular system 48 49 50 .

In a longer 2014 study 51 over four consecutive months, environmental temperature was modulated overnight – 24 ° C (run-in period), (cold acclimatisation), 24 ° C (wash-out period), and 30 ° C (heat acclimatisation). After a month of exposure to mild cold (19 ° C ), BAT volume and activity almost doubled, but after a month of exposure to warm temperature (30 ° C), BAT activity was negligible. The researchers commented that: “Remarkably, the increase in BAT activity following the cold acclimatisation was accompanied by a significant increase in postprandial glucose disposal, but only during mild cold exposure.

One study 52 looked at levels of irisin (a relatively newly discovered hormone) as a result of both intense exercise and cold exposure. Irisin is nicknamed the “exercise hormone” since  it’s released during moderate aerobic endurance activity and is known to be an anti-obesity and anti-diabetes hormone that regulates fat tissue and blood sugar, improving insulin sensitivity, bone quality/quantity 53 54 , and building lean muscle mass. In essence, irisin is thought to help reduce obesity by converting white fat to brown fat 55 . Being that irisin is released by muscles during physical exercise 56 , if cold-exposure also releases irisin, then perhaps the metabolic benefits of such exposure would be similar to those when irisin is released through exercise. And, indeed, this study demonstrated that this appears to be the case.

And irisin has other interesting effects. A study 57 on the reasons why healthy centenarians are healthy noted that they tend to have increased serum irisin levels, whilst irisin levels were significantly lower in younger patients with myocardial infarction 58 . So, although somewhat an aside to the main thrust of this blog, such findings are likely to prompt further research into the role of irisin in vascular disorders and life span extension.

Another hormone, adiponectin 59 , has associations with both BAT activation and centenarians. It’s been shown 60 that when BAT is activated through cold exposure, adiponectin levels increase within just two hours, resulting in a 70% increase in circulating adiponectin in adult men. Interestingly, both male and female centenarians (as well as their offspring) have been found 61  both to have genetics which boost adiponectin and to have generally higher circulating levels of adiponectin. This suggests a further link between BAT activation and longevity – this time because of the increased production of adiponectin. Furthermore, these high concentrations of plasma adiponectin in centenarians were associated 62 with other favourable metabolic factors as well as with lower levels of C-reactive protein 63  and E-selectin64 . It was mentioned earlier that BAT activation results in the production of FGF-21 – a hormone that improves insulin sensitivity and glucose metabolism. The latter benefits may explain why this hormone has been shown 46  to play a role in promoting longevity in humans.

In relation to fat and irisin, it was shown 65 that applying irisin to human preadipocytes (cells that can be transformed into different fat cells through the process of adipogenesis) , ordinary white adipocytes could be changed into beige adipocytes. This helps confirm the role of irisin as a myokine66 that can expand beige adipocyte mass, increasing the non-shivering thermogenesis capacity and, thereby, promoting a shift from inefficient and non-sustainable shivering thermogenesis to more efficient and sustainable non-shivering thermogenesis. In the following diagram, FGF-21 (fibroblast growth factor 21) promotes BAT’s activity of cold-induced non-shivering thermogenesis in humans.

Model of interplay between shivering and non-shivering thermogenesis. Exposure to cold promotes shivering in non-acclimated individuals, with the release of irisin. This response is unsustainable and costly from an energy-conservation perspective. Irisin promotes the expansion and differentiation of beige adipocytes, which increase resilience to cold enhancing non-shivering thermogenesis and delays the onset of shivering.

All the above studies indicate both that human BAT is extremely plastic, and that activation via cold exposure is necessary to generate a significant metabolic response.

Final thoughts

So, merely reducing the environmental temperature in your home could help to lose some body weight (represented by an additional energy expenditure of around 100 kcal) without actually undergoing exercise or changing one’s dietary habits. However, the amount of body fat you could lose through undergoing even colder and, consequently, more uncomfortable temperatures is something that I can’t imagine many people wanting to opt for as a weight-loss method.

Of course, integrating a bit of low temperature “therapy” might reduce one’s heating bills. And, of course, there is another weight-loss method associated with temperature modulation – namely, sweating your socks off in a sauna, albeit really just water that you’ll lose, and you’ll put the weight back on pretty soon afterwards when you rehydrate.

However, there is another simple non-exercise/non-dieting weight-loss method which is similar in effect to turning down the thermostat – namely, something called a standing desk. A standing desk is simply a matter of raising the height of one’s table (and hence the computer , book or paperwork thereon) and standing instead of sitting. Interestingly, this method has been shown 67 to increase calories burnt (in this case in young schoolchildren):

Another study 68 found that standing burned an extra 0.15 calories per minute, on average, compared with sitting. Men burned an extra 0.2 calories per minute while standing, which was twice as much as women, who burned an extra 0.1 calories. This was because men they typically have more muscle mass than women. This would mean that a person weighing around 63 kg (140 pounds/10 stones), replacing sitting with standing for six hours a day would burn an extra 54 calories per day.

Naturally, pharmaceutical companies may well try to come up with a “magic pill” that will stimulate BAT activity without the need for subjecting oneself to cold temperatures – maybe an injection or pill to stimulate BAT activity without having to ensure cold temperatures; but experience teaches us that most of these pharmaceutical wonder cures have unpleasant side effects and rarely prove as effective as their manufacturers initially claim.

So, whether of itself, or even when combined with another simple non-exercise/non-dietary change weight-loss method, it would seem that the benefits are interesting, though not comparable with the weight-loss benefits of a combination of exercise and eating a low-fat plant-based diet.

References & Notes

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  59. Adiponectin is a protein hormone that is produced by fat cells. Its physiological effects include the reduction of inflammation and atherogenesis (the formation of fatty deposits in the arteries) and enhancement of the response of cells to insulin. []
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  63. High C-reactive protein (CRP) levels in your blood indicate inflammation in your body, possibly indicating an infection or other condition. []
  64. E-selectin is also associated with inflammation, mediating leukocyte rolling (adhesion) on activated endothelial cells at inflammatory sites. It may also support tumour cell adhesion during hematogenous metastasis (cancer spread) and may play roles in angiogenesis (cancer development) and haematopoiesis (production of blood cells). []
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  66. A myokine is one of several hundred cytokines or other small proteins and proteoglycan peptides that are produced and released by muscle cells in response to muscular contractions. []
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