Brain ‘Switch’ tells Body to Burn Fat After a Meal

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Highlights •Diurnal changes in hypothalamic TCPTP coordinate feeding with energy expenditure •Feeding represses hypothalamic TCPTP to increase energy expenditure •TCPTP inhibits insulin signaling in AgRP neurons to repress energy expenditure •Insulin signaling in AgRP neurons increases the browning of white fat

Highlights
•Diurnal changes in hypothalamic TCPTP coordinate feeding with energy expenditure
•Feeding represses hypothalamic TCPTP to increase energy expenditure
•TCPTP inhibits insulin signaling in AgRP neurons to repress energy expenditure
•Insulin signaling in AgRP neurons increases the browning of white fat

 

Scientists at Monash University’s Biomedicine Discovery Institute have found a mechanism by which the brain coordinates feeding with energy expenditure, solving a puzzle that has previously eluded researchers and offering a potential novel target for the treatment of obesity. Obesity – a major risk factor for many diseases including cardiovascular disease, Type 2 diabetes, liver disease and several cancers – is at epidemic levels in Australia.

Researchers from the Metabolic Disease and Obesity Program have shown in lab models that feeding controls the ‘browning’ of fat, ie conversion of white fat, which stores energy, into brown fat, which expends it. Fat is stored in adipocytes, which can change from white to brown states and back again.

Their study shows that after a meal the brain responds to circulating insulin, which is increased after a rise in blood glucose. The brain then sends signals to promote the browning of fat to expend energy. By contrast, after a fast, the brain instructs these browned adipocytes to once more convert into white adipocytes, storing energy. These processes help prevent both excess weight gain and excess weight loss in response to feeding and fasting, meaning body weight remains relatively stable over time.

The brain’s ability to sense insulin and coordinate feeding with energy expenditure via browning is controlled by a switch-like mechanism turned on after fasting to inhibit the response to insulin, repressing browning and conserving energy, and turned off after feeding to facilitate the insulin response to promote browning and to expend energy. “What happens in the context of obesity is that the switch stays on all the time – it doesn’t turn on off during feeding,” Professor Tony Tiganis said.

“As a consequence, browning is turned off all the time and energy expenditure is decreased all the time, so when you eat, you don’t see a commensurate increase in energy expenditure – and that promotes weight gain,” Professor Tiganis said. Previous investigations by the researchers that showed how the brain coordinates white adipose tissue browning attracted considerable attention after it was published in early 2015.

The researchers are further exploring the possibility of inhibiting the switch for therapeutic purposes to promote the shedding of excess fat. “Obesity is a major and leading factor in overall disease burden worldwide and is poised, for the first time in modern history, to lead to falls in overall life expectancy,” Professor Tiganis said.
https://www.monash.edu/medicine/news/latest/articles/revealed-brain-switch-tells-body-to-burn-fat-after-a-meal http://linkinghub.elsevier.com/retrieve/pii/S1550413117304345