A protein has been identified by researchers from the Okinawa Institute of Science and Technology Graduate University (OIST) that plays a key role in how the brain regulates appetite and metabolism.
Loss of the protein, XRN1, from the forebrain, resulted in obese mice with an insatiable appetite. The findings of the study were published in the journal ‘iScience’.
Obesity is a growing public health concern, with over 650 million adults worldwide designated as obese. The condition has been linked to many disorders, including cardiovascular disease, type 2 diabetes and cancer.
“Fundamentally, obesity is caused by an imbalance between food intake and energy expenditure,” said Dr Akiko Yanagiya, a researcher in the Cell Signal Unit at OIST, headed by Professor Tadashi Yamamoto.
In the study, the scientists created mice that were unable to produce the protein, XRN1, in a subset of neurons in the forebrain. This brain region includes the hypothalamus, an almond-sized structure that releases hormones into the body, helping to regulate body temperature, sleep, thirst and hunger.
At 6-weeks-old, the scientists noticed that the mice without XRN1 in the brain rapidly began to gain weight and became obese by 12 weeks of age. Fat accumulated in the mice’s body, including within adipose tissue and the liver. When they monitored feeding behaviour, the team found that the mice without XRN1 ate almost twice as much each day as the control mice.
“This finding was really surprising. When we first knocked out XRN1 in the brain, we didn’t know exactly what we would find, but this drastic increase in appetite was very unexpected,” said Dr Shohei Takaoka, a former PhD student from the OIST Cell Signal Unit.
To investigate what might be causing the mice to overeat, the scientists measured the blood levels of leptin — a hormone that suppresses hunger. Compared to the controls, the level of leptin in the blood was abnormally high, which would normally stop the mice from feeling hungry. But unlike the control mice, the mice without XRN1 didn’t respond to the presence of leptin — a condition known as leptin resistance.
The scientists also found that 5-week-old mice were resistant to insulin, a hormone that is released by beta cells in the pancreas in response to the high levels of blood glucose that occur after eating.
This type of failure in how the body responds to glucose and insulin can ultimately lead to diabetes. As the mice got older, levels of glucose and insulin in the blood rose significantly alongside the increased leptin levels.
The scientists then checked whether the obesity was also driven by the mice using less energy. They placed each mouse in a special cage that measured how much oxygen the mice used to indirectly work out their metabolic rate.
In the mice aged 6 weeks, the scientists didn’t find an overall difference in energy expenditure. However, they found something very surprising. The mice without XRN1 were mainly using carbohydrates as an energy source, while the control mice were able to switch between burning carbohydrate at night, when they were most active, and fat during the day, when less active.
“For some reason, this means that without XRN1, the mice cannot use fat as a fuel effectively. Why this occurs though, we still don’t know,” said Dr Yanagiya.
Once the mice reached 12 weeks of age, their energy expenditure decreased compared to control mice. But, the scientists believed, this was an effect of obesity, due to the mice being less active, rather than a cause.
To further investigate how the loss of XRN1 results in leptin resistance and an increased appetite, the scientists looked at whether the activity of appetite-regulating genes changed within the hypothalamus.
In the hypothalamus, the scientists found that the mRNA used to make the protein Agouti-related peptide (AgRP) — one of the most potent stimulators of appetite — was elevated in the obese mice, leading to higher amounts of AgRP protein.
“It’s still only speculation, but we think that an increase of this protein, and abnormal activation of the neuron that produces it, might be the cause of leptin resistance in these mice,” said Dr Yanagiya.
