5 Ways to Turn Belly Fat into Body Heat (brown fat activation)

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Ways to Turn Belly Fat into Body Heat (brown fat activation) - Thomas DeLauer
Cold Therapy

One study, published in the Journal of Clinical Investigation, looked at 12 young men with lower-than-average amounts of active brown fat who were asked to sit in a 63-degree Fahrenheit room for two hours a day over the course of six weeks

They burned an extra 108 calories in the cold compared with normal indoor temperatures - after six weeks their bodies were burning an extra 289 calories in the cold, prompting researchers to hypothesize that the exposure to lower temps increased the activity of a gene that converts white fat to brown

https://www.jci.org/articles/view/67803

Why This Is

A study published in the journal Nature found that low temperature exposure causes stem cells to form brown fat instead of white fat

Specifically, to induce adipocyte browning using bone marrow (BM) derived mesenchymal stem cells (MSC), there is a temperature differentiation at 32 °C instead of 37 °C (lowered from 37 to 32 degrees)

The low temperature promoted browning in adipogenic cultures, with increased adipocyte differentiation and upregulation of adipogenic and thermogenic factors, especially UCP1

https://www.nature.com/articles/s41598-018-23267-9

Fasting

*Fasting-induced adipose-VEGF induces M2 macrophage activation, which triggers WAT browning*

https://www.nature.com/articles/cr2017126

Ketosis

A study published in the International Union of Biochemistry and Molecular Biology found that a keto diet increases brown adipose tissue mitochondrial proteins and UCP1 levels in mice

Mice were put on either a keto diet or a regular chow diet - in the keto group, blood glucose levels were 30% lower while D-β-hydroxybutyrate levels were about 3.5-fold higher

Median mitochondrial size in the interscapular BAT (IBAT) of the KD group was about 60% greater, whereas the median lipid droplet size was about half of that in the chow group. Mitochondrial oxidative phosphorylation proteins were increased (1.5–3-fold) and the uncoupling protein 1 levels were increased by threefold in mice fed the KD

AMP levels were 60% higher in the KD group and cAMP response element binding protein was 2.5-fold higher, suggesting increased sympathetic system activity.

demonstrate that a KD can also increase BAT mitochondrial size and protein levels.

The KD increased markers of sympathetic activity (cAMP and CREB levels) in the BAT of the mice.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3821007/

HIIT

A study published in Diabetology & Metabolic Syndrome looked at the effects of aerobic training (15) vs HIIT (15) in female adolescents

The session of aerobic exercise included cycling at 65% of their peak heart rate (HRpeak) for 40 min. In the HIIT group, exercise included six bouts of 1 min at 85–95% HRpeak separated by 1 min of recovery

Levels of expression of irisin in skeletal muscle increased significantly after a session of HIIT (p less than 0.05), while aerobic exercise no effect on irisin levels

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746008/

Exercise causes muscle cells to release a protein hormone called irisin - Irisin acts upon white fat to alter it by giving it properties of brown fat by increasing the number of mitochondria within the white fat cells, changing the color of the fat cells to beige cells - essentially mimicking brown fat’s effects

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746008/

Turmeric

A study published in Biochemical and Biophysical Research Communications found that curcumin promotes browning of white adipose tissue in a norepinephrine-dependent way

Specifically, curcumin promotes β3AR gene expression in inguinal WAT and elevates the levels of plasma norepinephrine, a hormone that can induce WAT browning

https://www.ncbi.nlm.nih.gov/pubmed/26362189
Additional Resources

1)https://www.sciencedirect.com/science/article/pii/S1550413113001125
2)https://nature.berkeley.edu/news/2018/03/brown-fat-flexes-its-muscle-burn-energy
3)https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746008/

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