Researchers in South Korea have uncovered mechanisms behind the enzyme that controls our appetite. Understanding how our appetite is controlled and influenced by our body and brain is important for countering the worldwide obesity epidemic.
To maintain a healthy energy balance, our appetite needs to increase or decrease, depending on our caloric intake through food and energy use in our daily lives. Previous research has shown that a region of the brain, known as the hypothalamus, senses levels of sugar (e.g., glucose) and hormones (e.g., leptin) in the blood, and uses these signals to regulate food intake. However, many questions remain about the mechanisms by which the hypothalamus does this.
Now a team of researchers at the Daegu Gyeongbuk Institute of Science and Technology (DGIST) has discovered that a low-glucose condition activates a hypothalamic enzyme called adenosine monophosphate-activated protein kinase (AMPK), which changes the properties of small protein-like molecules, called neuropeptides, which our brain uses to communicate. It does so by taking advantage of a natural “self-destruct” mechanism called autophagy. This process allows our body to recycle and degrade cellular materials.
By way of analogy, imagine a movie where the hypothalamus is the director who sets the scene in motion by activating AMPK. The researchers have discovered how the brain instructs its two key “actors” to do their job. The first “actor” is a neurohormone called neuropeptide Y (NPY), while the second is another neurohormone produced in the hypothalamus called pro-opiomelanocortin-alpha (POMC). The director activates AMPK, which sets increased autophagy in motion. This in turn influences how our actors, NPY and POMC, behave on a genetic level similar to a movie that tells a story of increased food intake and body weight.
The big challenge for researchers was to untangle the hundreds of possible pathways between the brain and body, in the form of hormones, enzymes and other chemical messengers that might be responsible. By individually blocking off different pathways and activating or de-activating chemical messengers in turn, the researchers were able to determine the brain’s appetite control systems, much like how one might remove actors from a film and see what parts of the story are lost or no longer make sense in the script.
By demonstrating how AMPK-activated autophagy controls the expression of neurohormones in the brain’s hypothalamus, researchers are one step closer to understanding the dynamics of our eating behavior. The next step is to untangle how autophagy itself modulates (up or down) our brain’s neurohormones, such as NPY, to regulate our appetite.
This story is reprinted from materials provided by the Daegu Gyeongbuk Institute of Science and Technology (DGIST).