A dieter wrestling with
cravings for fatty foods might be tempted to blame their tongue: the delicious
taste of butter or ice cream is hard to resist. But new research investigating
the source of our appetites has uncovered an entirely new connection between
the gut and the brain that drives our desire for fat.
At Columbia’s Zuckerman Institute, scientists studying mice found that fat entering the
intestines triggers a signal. Conducted along nerves to the brain, this signal
drives a desire for fatty foods. Published on September 7, 2022 in Nature, the new study raises the possibility of interfering
with this gut-brain connection to help prevent unhealthy choices and address
the growing global health crisis caused by overeating.
“We live in unprecedented times, in
which the overconsumption of fats and sugars is causing an epidemic of obesity
and metabolic disorders,” said first author Mengtong Li, PhD, a postdoctoral researcher in the lab of the
Zuckerman Institute’s Charles Zuker, PhD, supported by the Howard Hughes Medical
Institute. “If we want to control
our insatiable desire for fat, science is showing us that the key conduit
driving these cravings is a connection between the gut and the brain.”
This new view of dietary choices and
health started with previous work from the
Zuker lab on sugar. Researchers
found that glucose activates a specific gut-brain circuit that communicates to
the brain in the presence of intestinal sugar. Calorie-free artificial
sweeteners, in contrast, do not have this effect, likely explaining why diet
sodas can leave us feeling unsatisfied.
Our research is showing that the tongue tells our
brain what we
like. Our brain what we need.
“Our research is showing that the tongue
tells our brain what we like, such as things that taste sweet, salty or fatty,”
said Dr. Zuker, who is also a professor of biochemistry and molecular
biophysics and of neuroscience at Columbia’s Vagelos College of
Physicians and Surgeons. “The
gut, however, tells our brain what we want, what we need.”
Dr. Li wanted to explore how mice
respond to dietary fats: the lipids and fatty acids that every animal must
consume to provide the building blocks of life. She offered mice bottles of
water with dissolved fats, including a component of soybean oil, and bottles of
water containing sweet substances known to not affect the gut but that are
initially attractive. The rodents developed a strong preference, over a couple
of days, for the fatty water. They formed this preference even when the
scientists genetically modified the mice to remove the animals’ ability to
taste fat using their tongues.
“Even though the animals could not taste
fat, they were nevertheless driven to consume it,” said Dr. Zuker.
The researchers reasoned that fat must
be activating specific brain circuits driving the animals’ behavioral response
to fat. To search for that circuit, Dr. Li measured brain activity in mice
while giving the animals fat. Neurons in one particular region of the
brainstem, the caudal nucleus of the solitary tract (cNST), perked up. This was
intriguing because the cNST was also implicated in the lab’s previous discovery of the neural basis of sugar preference.
Dr. Li then found the communications
lines that carried the message to the cNST. Neurons in the vagus nerve, which
links the gut to the brain, also twittered with activity when mice had fat in
their intestines.
Having identified the biological
machinery underlying a mouse’s preference for fat, Dr. Li next took a close
look at the gut itself: specifically the endothelial cells lining the
intestines. She found two groups of cells that sent signals to the vagal
neurons in response to fat.
“One group of cells functions as a
general sensor of essential nutrients, responding not only to fat, but also to
sugars and amino acids,” said Dr. Li. “The other group responds to only fat,
potentially helping the brain distinguish fats from other substances in the
gut.”
Dr. Li then went one important step
further by blocking the activity of these cells using a drug. Shutting down
signaling from either cell group prevented vagal neurons from responding to fat
in the intestines. She then used genetic techniques to deactivate either the
vagal neurons themselves or the neurons in the cNST. In both cases, a mouse
lost its appetite for fat.
“These interventions verified that each
of these biological steps from the gut to the brain is critical for an animal’s
response to fat,” said Dr. Li. “These experiments also provide novel strategies
for changing the brain’s response to fat and possibly behavior toward food.”
The stakes are high. Obesity rates have nearly doubled worldwide since 1980. Today, nearly half a billion people suffer from diabetes.
“The overconsumption of cheap, highly
processed foods rich in sugar and fat is having a devastating impact on human
health, especially among people of low income and in communities of color,”
said Dr. Zuker. “The better we understand how these foods hijack the biological
machinery underlying taste and the gut-brain axis, the more opportunity we will
have to intervene.”
Scott Sternson, PhD, a professor of neuroscience
at University of California, San Diego, who was not involved in the new
research, highlighted its potential for improving human health.
“This exciting study offers insight about the molecules and cells that compel animals to desire fat,” said Dr. Sternson, whose work focuses on how the brain controls appetite. “The capability of researchers to control this desire may eventually lead to treatments that may help combat obesity by reducing consumption of high-calorie fatty foods.”
Source: https://zuckermaninstitute.columbia.edu/cravings-fatty-foods-traced-gut-brain-connection
Journal article: https://www.nature.com/articles/s41586-022-05266-z
Image: Vagal neurons that carry signals
from the gut to the brain (nuclei shown in blue), with cells responsible for
fat preference in green. (Mengtong Li / Zuker lab / Columbia’s Zuckerman Institute
Source: Cravings
for Fatty Foods Traced to Gut-Brain Connection – Scents of Science
(myfusimotors.com)
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