Molecular Imaging News
October 23, 2006
PET Study Offers New Clues to Brain-Stomach Interaction
Findings implicate brain circuits involved in drug craving and emotional response to food
Researchers at the U.S. Department of Energy’s Brookhaven National Laboratory have found new clues to how the brain and the stomach interact with emotions to cause overeating and obesity. By looking at how the human brain responds to “fullness” messages sent to the brain by an implanted device that stimulates the stomach, the scientists have identified brain circuits that motivate the desire to overeat in the obese—the same circuits that cause addicted individuals to crave drugs. The scientists have also verified that these circuits play a critical role in eating behaviors linked to soothing negative emotions. The study appears in the October 17, 2006 issue of the Proceedings of the National Academy of Sciences.
“This study opens new territory in understanding how the body and brain connect to each other, and how this connection is tied to obesity,” said lead author Gene-Jack Wang of Brookhaven Lab’s Center for Translational Neuroimaging. “We were able to simulate the process that takes place when the stomach is full, and for the first time we could see the pathway from the stomach to the brain that turns ‘off’ the brain’s desire to continue eating.”
Wang, a member of SNM, and colleagues used positron emission tomography (PET) to study the brain metabolism of seven obese individuals who had gastric stimulators implanted for one to two years. The stimulator, an investigational device much like a pacemaker, provides low levels of electrical stimulation to the vagus nerve, causing the stomach to expand and produce peptides that send messages of fullness to the brain. The device has been shown to reduce the desire to eat. This study provides the first direct evidence of which brain regions are involved in this response and gives new clues to how satiety signals sent by the stomach affect eating behavior.
Participants in the study received two PET scans two weeks apart: one with the gastric stimulator on, the other with the stimulator off. Participants were not told whether their stimulator was on or off. Prior to the scans, subjects were injected with a radioactively labeled form of glucose, which the scanner could track to monitor brain metabolism.
“We found that implantable gastric stimulators induced significant changes in metabolism in brain regions associated with controlling emotions, effectively shutting down these obese subjects’ desire to eat,” said Wang.
The changes were particularly pronounced in the hippocampus, where metabolism was 18 percent higher during gastric stimulation. The hippocampus is linked with emotional behaviors, learning and memory, and processing of sensory and motor impulses. The hippocampus also plays a role in the retention of memories related to prior drug experiences in addicted individuals, implying that memories of satiety in the obese might also be stimulated by hippocampal activation.
The stimulators also sent messages of satiety to brain circuits in the orbitofrontal cortex and striatum, which have been linked to craving and desire for drugs in drug-addicted patients.
At each brain scanning session, participants were also asked to answer a questionnaire, which measured three aspects of eating behavior: cognitive restraint, uncontrolled eating, and emotional eating. The questionnaire determined correlations between eating behaviors and areas of the brain activated by the stimulator. During gastric stimulation, scores on a measure of self-described “emotional eating” were 21 percent lower than when the stimulator was off.
“This provides further evidence of the connection between the hippocampus, the emotions, and the desire to eat, and gives us new insight into the mechanisms by which obese people use food to soothe their emotions,” said Wang. “This new pathway should be explored in further studies to determine if there are any implications for treating or preventing obesity.”