Summary: Researchers report the brain’s ability to sense insulin and coordinate feeding with energy expenditure is controlled by a mechanism that is turned on after fasting to inhibit insulin response and conserve energy. After feeding, the mechanism is turned off to facilitate insulin response and expend energy. However, in obese people, researchers believe the switch may stay on all the time.
Source: Monash University.
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 laboratory models that feeding controls the ‘browning’ of fat, that is, the conversion of white fat, which stores energy, into brown fat, which expends it. Fat in the human body is stored in specialised cells called adipocytes, which can change from white to brown states and back again.
Their study, published in Cell Metabolism today, 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 researchers showed that 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,” lead researcher 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.
“For a long time, the missing piece to the puzzle was always why this occurs in the body,” first author Dr Garron Dodd said.
“We’ve shown not only why this occurs but also the fundamental mechanism involved. It’s very exciting,” Dr Dodd said.
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.
“What our studies have shown is that there is a fundamental mechanism at play that normally ensures that energy expenditure is matched with energy intake. When this is defective, you put on more weight. Potentially we may be able to rewire this mechanism to promote energy expenditure and weight loss in obese individuals. But any potential therapy is a long way off,” he said.
About this neuroscience research article
Researchers from Germany collaborated on the study.
Funding: This research was supported by the Australian National Health and Medical Research Council.
Source:Monash University Image Source: NeuroscienceNews.com image is in the public domain. Original Research: Abstract for “A Hypothalamic Phosphatase Switch Coordinates Energy Expenditure with Feeding” by Garron T. Dodd, Zane B. Andrews, Stephanie E. Simonds, Natalie J. Michael, Michael DeVeer, Jens C. Brüning, David Spanswick, Michael A. Cowley, and Tony Tiganis in Cell Metabolism. Published online August 1 2017 doi:10.1016/j.cmet.2017.07.013
Cite This NeuroscienceNews.com Article
[cbtabs][cbtab title=”MLA”]Monash University “Brain Switch Tells Body to Burn Fat After a Meal.” NeuroscienceNews. NeuroscienceNews, 28 August 2017. <https://neurosciencenews.com/fat-burning-neuroscience-7215/>.[/cbtab][cbtab title=”APA”]Monash University (2017, August 28). Brain Switch Tells Body to Burn Fat After a Meal. NeuroscienceNew. Retrieved August 28, 2017 from https://neurosciencenews.com/fat-burning-neuroscience-7215/[/cbtab][cbtab title=”Chicago”]Monash University “Brain Switch Tells Body to Burn Fat After a Meal.” https://neurosciencenews.com/fat-burning-neuroscience-7215/ (accessed August 28, 2017).[/cbtab][/cbtabs]
A Hypothalamic Phosphatase Switch Coordinates Energy Expenditure with Feeding
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
Summary Beige adipocytes can interconvert between white and brown-like states and switch between energy storage versus expenditure. Here we report that beige adipocyte plasticity is important for feeding-associated changes in energy expenditure and is coordinated by the hypothalamus and the phosphatase TCPTP. A fasting-induced and glucocorticoid-mediated induction of TCPTP, inhibited insulin signaling in AgRP/NPY neurons, repressed the browning of white fat and decreased energy expenditure. Conversely feeding reduced hypothalamic TCPTP, to increase AgRP/NPY neuronal insulin signaling, white adipose tissue browning and energy expenditure. The feeding-induced repression of hypothalamic TCPTP was defective in obesity. Mice lacking TCPTP in AgRP/NPY neurons were resistant to diet-induced obesity and had increased beige fat activity and energy expenditure. The deletion of hypothalamic TCPTP in obesity restored feeding-induced browning and increased energy expenditure to promote weight loss. Our studies define a hypothalamic switch that coordinates energy expenditure with feeding for the maintenance of energy balance.
“A Hypothalamic Phosphatase Switch Coordinates Energy Expenditure with Feeding” by Garron T. Dodd, Zane B. Andrews, Stephanie E. Simonds, Natalie J. Michael, Michael DeVeer, Jens C. Brüning, David Spanswick, Michael A. Cowley, and Tony Tiganis in Cell Metabolism. Published online August 1 2017 doi:10.1016/j.cmet.2017.07.013