Body Fat - Friend or Foe? - #HP-EVOO - Blog # 83
Hello Everyone! Welcome back to another Friday blog. Today I wanted to take a closer look at BODY fat. Did you know AT (adipose tissue), or fat is actually an organ embedded in a dense network of blood vessels? Fat is really our friend…unless we allow it to grow out of control - then it becomes our foe. The type and amount of AT we carry on our body is extremely crucial. Let’s delve in.
Color dictates the type of AT (adipose tissue):
1. WAT (white adipose tissue) - White color is due to a large lipid droplet with low numbers of mitochondria, “which not only stores energy in the form of triglycerides but also is recognized as an important endocrine and immune organ.” WAT secretes several peptide hormones (leptin), cytokines, angiotensinogen, plasminogen activator inhibitor-1 (PAI-1), adiponectin, resistin, steroid hormones, adipsin and adulation-stimulating protein (ASP).
“Virtually all known adipose secreted proteins are dysregulated when the WAT mass is markedly altered, either increased in the obese state or decreased in lipoatrophy.” This is why obese or very thin/frail individuals have a higher risk of “all-cause”mortality, including Covid-19 or any other infection.
As adipocytes in AT grow and expand, they seek out new blood vessels to supply themselves. “With a high nutrient availability, the adipocytes store lipids in lipid droplets, and as their size expands oxygen availability is reduced. This mild hypoxic status can induce angiogenesis and remodeling of extracellular matrix to reduce hypoxia (Crewe et al., 2017).” So, if we keep over-eating, these cells get bigger and bigger until they need new ones to hold more fuel. Now, there are more cells requiring even greater blood supply. “In healthy AT, the vessels are lined by a single monolayer of quiescent ECs, which can rapidly switch to the angiogenic/proliferative state in the presence of angiogenic and metabolic signals to form new blood vessels (Draoui et al., 2017). AT produces and secretes various angiogenic factors such as angiopoietin-2 (Angpt2) and vascular endothelial growth factor (VEGF) as well as adipokines such as leptin and adiponectin, which influence and modulate angiogenesis and the vascular structure.” WAT is deposited in 2 general areas, on the viscera (organs) and under the skin.
- Subcutaneous fat - this is the jiggly fat - can be lumpy, muffin top, under arms, hips and thighs, jowls, etc…This type of fat is more protective and cushions our bony prominences.
- VAT (visceral adipose tissue) - in body cavity - cushions the organs - too much can squeeze our organs - very much like too many styrofoam peanuts pressing on a fragile lightbulb in a box. This is the dangerous fat. It’s THE FAT WE CAN’T SEE. It can occur in a skinny person or an obese person.
2. BAT (brown adipose tissue) - BAT is characterized by multiple small lipid droplets and many mitochondria - resulting in brown color. This is the GOOD FAT! It “uniquely expresses UCP-1 (uncoupling protein 1), enabling it to be specialized for energy expenditure and thermogenesis.” UCP-1 is a primary mitochondrial uncoupler - check out blog # 73 - that stimulates mitochondrial replication and browning of fat due to increased mitochondrial number.
Non-shivering thermogenesis is hormone-dependent. The hypothalamus produces TSH (thyroid stimulating hormone) signaling the thyroid to make thyroid hormone. It also signals the adrenal medulla to release norepinephrine that in the presence of T3 (active thyroid hormone) results in production of UCP-1 stimulating brown fat. BAT is metabolically very active and serves to supply heat to the organs.
Babies have LOTS of brown fat and have a racing metabolism. Adults have a paper-thin brown fat layer pressed near the bone, under your arms, sternum, back and abdomen and works like a space heater for your organs. When turned on It draws energy from WAT for power - literally burning away your white fat. “BAT expands when an organism is exposed to prolonged cold conditions and is linked with increased insulin sensitivity.”
3. Brite/beige Adipose Tissue - this type of fat occurs during transition:
- “whitening” of BAT. “Chronic obesity damages the cytoarchitecture of brown adipose tissue (BAT), leading to whitening of brown adipocytes and impaired thermogenesis, characterizing BAT dysfunction.” This is the beginning of weight-gain and progression toward metabolic syndrome. We lose the ability to generate heat appropriately. As inflammation rises, we lose mitochondrial function.
- “browning” of WAT: There are several ways we can “brown” our WAT - through exercise, weight-loss, improving vitamin D status, polyphenols in HP-EVOO HT (hydroxytyrosol) and oleocanthal, carotenoids and other phytonutrients, IF (intermittent fasting) and hormesis (temporary stress that stimulate healing) - particularly exposure to cold. In fact, exposure to cold (acute and chronic) activate BAT 41.6% over insulin. “Cold- and exercise-induced beiging increases the number of metabolically active cells within WAT depots, which in turn constitutes an effective strategy to combat obesity and T2DM.”
Fat is our Friend: Embryonically, fat is the third tissue formed following blood vessels and nerves - demonstrating its importance! Small bubbles of fat (think of bubble-wrap) form around the nerves and blood vessels, serving as fuel tanks for growth and development. I actually noticed this fat surrounding the neuro-vascular bundle on cadaver dissection! Now it makes sense!! “During development, the human fetus accrues the highest proportion of fat of all mammals.” AT is vital and serves as a fuel/storage tank for triglycerides as well as regulating the production of hormones like angiotensin factors and cytokines. AT is directly involved in energy homeostasis of the body - is in control of the “Goldilocks” sweet spot of just enough and not too much.
Foe: “AT expands through the increase in fat cell size (hypertrophy) and/or fat cell number (hyperplasia). The plasticity and expansion of AT is related to its angiogenic capacities. That is how good it is at stimulating growth of new blood vessels to supply itself. Angiogenesis is a tightly orchestrated process, which involves endothelial cell (EC) proliferation, migration, invasion, and new tube formation. The expansion of AT is accelerated by hypoxia, inflammation, and structural remodeling of blood vessels.” This is very similar to how cancer grows, stimulating angiogenesis to fuel its growth. When deposition of AT out-paces the growth of supplying blood vessels, the center of the expanding fat mass becomes very hypoxic and cell death occurs. This releases inflammatory cytokines driving up chronic inflammation. This is very dangerous!! This is why obesity is associated with IR, T2D, CVD, cancer, Alzheimer’s and more.
When we chronically over-consume and carry too much WAT on our body, it CRUSHES our metabolism (not the other way around), CRUSHES our major internal organs and LEAKS inflammatory hormones and cytokines into the body driving up chronic inflammation and the growth of more fat. Recent research has identified 4 phases of human metabolism. When excess fat is removed, we all share the same metabolism. 😳 WHAT???!!!! Have we not all thought - my metabolism is just slow. That’s why I’m gaining weight. Now we know, it’s the other way around - unhealthy fat is crushing our metabolism. Here are the phases: FYI - 60 is the new 20!!!
Phase 1 - birth to 1 year - super-high metabolic phase. Phase 2- ages 2-20 we gradually slow rate of metabolism to adulthood. Phase 3 from 20-60. THIS IS INCREDIBLE!!! This means we can DO something about it. We have control. Removing excess fat RESTORES our metabolism whether you are 20 or 60. The 4th phase is from 60-90 where the drop is roughly 17%.
The more weight we gain around our waist, the closer we get to CVD (cardiovascular disease), IR (insulin resistance), T2D (type 2 diabetes), Alzheimer’s and dementia. Even people skinny on the outside can have fat literally pressing on and crushing their viscera, diminishing organ function, driving HTN (hypertension), IR, CVD, T2D, lipid: triglyceride and cholesterol imbalance, CKD (chronic kidney disease) and more.
Interestingly, one of the first places we start accumulating WAT isn’t our waist - it is our tongue! The base including the posterior 1/3 of the tongue becomes marbled like a ribeye - tongue volume increases with weight-gain. This explains how even skinny people can have sleep apnea and why obese individuals can have severe obstructive sleep apnea. One of the first clues that you are gaining weight is that you are starting to snore.
Hormones released from WAT control sensitivity to insulin, release of inflammatory process mediators - several cytokines, including IL-6 (interleukin-6) and stimulation of metabolic pathways. Here are some of the primary hormones released:
- Leptin - satiety hormone
- Ghrellin - hunger hormone
- Cytokinies- many are inflammatory (IL-6)
- adipsin - helps insulin bring glucose into the cell - “T2DM patients with β cell failure are deficient in adipsin.”
- visfatin - has insulin-mimetic actions and is produced in VAT secreted in parallel with obesity. It promotes insulin-resistance along with LPS, IL-1β, TNFα and IL-6. Its levels are also increased in acute lung inflammation and sepsis, which is accompanied by an insulin-resistant state.
- Angiotensinogen - part of the system regulating blood pressure. Elevated levels are associated with predisposition to hypertension.
- Aromatase - Excreted from belly fat - in men with belly fat, testosterone gets converted to estrogen, creating “man boobs” and soft skin. In women with belly fat, it makes androgens, creating male-pattern hair loss and facial hair growth.
- Adiponectin - This protective hormone is more prevalent than any other hormone - it is the gas pedal on metabolism, improving uptake of nutrients, lowering inflammation and preventing metabolic syndrome. “Circulating adiponectin concentrations are reduced in obese individuals, and this reduction has been proposed to have a crucial role in the pathogenesis of atherosclerosis and cardiovascular diseases associated with obesity and the metabolic syndrome.” Adiponectin does many things:
- Increases utilization of FAs (fatty acids) and glucose in skeletal muscle
- Protects pancreatic β cell
- Decreases fat deposition in skeletal muscle
- Increases AMPK and PPAR-a in skeletal muscle
- Decreased hepatic (liver) glycogenolysis (breakdown of glycogen)
- Decreases hepatic gluconeogenesis (production of glucose)
- Increases catabolism of vLDL
- Increases HDL
- Decreases triglycerides
- Decreases ROS and inflammatory cytokines (IL-6)
- Decreases CRP and inflammatory markers
- Decreases TNF-a adhesion on human aortic endothelium and inhibits other adhesion molecules from adhering to endothelium
- Resistin - resists insulin from pulling sugar out of the blood. It is putting the brakes on metabolism. When adiponectin levels are high enough, resistin is low. When adiponectin levels drop, we become insulin-resistant. Elevated resistin level is intimately involved in obesity, inflammation, IR, T2D and stress-response mechanisms.
Okay, so most of us want to increase our BAT, decrease our WAT and restore our metabolism to the way it was when we were 20. This means removing VAT - fat from our liver, pancreas, heart…the fat we can’t see. Did you know HP-EVOO is amazing at this? Check out my personal journey - blog # 22! Take a shot in the am -when you are most insulin-sensitive. This information tells your body to burn stored fat!!! There are many ways that we can stimulate this pathway, restoring mitochondrial function, metabolism, and ultimately health and longevity.
- Support thyroid health - UCP-1 requires T3 (selenium and iodine) - eat seaweed, Brazil nuts…
- Vitamin D3 - hormone highly involved in anti-inflammatory and immune function - get sunshine - supplement in winter - get it tested on blood work. You want your levels >50, ideally 60-80. Make sure to get K2, they work together to take calcium from your arteries and put it in your bones!
- Magnesium - is a cofactor for the insulin receptor!!! Magnesium is required for mitochondrial function and ATP activation. 48% of T2D are deficient - your risk of T2D goes up 79% if you are low in magnesium!
- Exercise - stimulates the browning of WAT
- IF - intermittent fasting. We naturally fast when we are sleeping. Extend this time as long as possible to extend fat-burning. This allows your body to stay in autophagy - shoot for 14-18 hours.
- Cold Exposure - a cold plunge <59 degrees - is amazing at activating BAT. Take a hot shower followed by a cold shower or plunge. Cold/winter swimming studies show 11 minutes exposure per week significantly increases BAT. This stimulates both our sympathetic nervous system and our parasympathetic nervous system. This increases norepinephrine and dopamine in the brain by 2.5% - and can last for hours.
- Omega 3s - DHA, EPA, ALA - improve insulin-sensitivity, improves metabolism, activates BAT, balances cholesterol
- Increase adiponectin levels - lose weight
- Carotinoids - astaxanthin, lycopene, zeaxanthin…
- HP-EVOO - (high polyphenol extra virgin olive oil) - HT (hydroxytyrosol) and oleocanthal are 2 major polyphenols that are anti-inflammatory, healing to the liver and goes a long way to remove harmful VAT.
We will add K2 to our supplements.