Medicines such as Semaglutide & Tirzepatide are
becoming very popular for treating diabetes and
helping people lose weight. These drugs work by
copying a natural hormone in the body called GLP-1,
which is released after eating. This hormone sends
signals to the brain that reduce hunger and help
people feel full for longer. New research shows that
GLP-1 drugs affect several important areas of the
brain, not just the hunger center. Scientists have
found that these medicines also act on brain regions
that control nausea, pleasure-based eating,
behavior, and even thirst. This explains why many
people taking these drugs eat less, crave fewer
“junk foods,” and sometimes feel nauseated or less
thirsty. One part of the brain called the area
postrema, also known as the brain’s vomiting center,
appears to be responsible for both weight loss and
nausea. This means the same brain pathway may cause
helpful effects as well as unwanted side effects.
Another brain area, the amygdala, is involved in
reducing pleasure-driven eating by lowering
dopamine, a chemical linked to reward and cravings.
In animal studies, researchers found that combining
low doses of a GLP-1 drug with another hormone,
oxytocin, led to significant weight loss without
causing nausea. This raises hope that future
treatments may reduce side effects while keeping the
benefits. Overall, these discoveries suggest that
GLP-1 drugs work through complex brain networks.
Understanding these pathways may lead to safer and
more effective treatments for obesity in the future. |