New Discovery Could Lead to Improved Weight Loss Treatments
By SCRIPPS RESEARCH
Scientists from Scripps Research have made a breakthrough that could pave the way for new weight loss and metabolic health therapies.
When
exposed to cold temperatures, mammals instinctively burn more energy to keep
their body temperature stable. This surge in energy usage prompts an increase
in appetite and feeding although the specific mechanism controlling this is
unknown.
Neuroscientists
at Scripps Research have now pinpointed the brain
circuits responsible for this increased appetite during low temperatures.
In
the new study, recently published in the journal Nature, the researchers identified a cluster of neurons
that work as a “switch” for this cold-related, food-seeking behavior in mice.
The discovery could lead to potential therapeutics for metabolic health and
weight loss.
“This is a fundamental adaptive mechanism in mammals and targeting it with future treatments might allow the enhancement of the metabolic benefits of cold or other forms of fat burning,” says study senior author Li Ye, PhD, associate professor and the Abide-Vividion Chair in Chemistry and Chemical Biology at Scripps Research.
The
study’s first author was Ye Lab postdoctoral research associate Neeraj Lal,
PhD.
Because exposure to cold leads to enhanced energy burning to stay warm, cold water immersion and other forms of “cold therapy” have been explored as methods for losing weight and improving metabolic health.
One drawback of cold therapies is that humans’ evolved responses to cold are not designed to cause weight loss (an effect that could have been fatal during the frequent periods of food scarcity in pre-modern times).
Cold, like dieting and exercise, increases
appetite to counteract any weight-loss effect. In the study, Ye and his team
set out to identify the brain circuitry that mediates this cold-induced
appetite increase.
One
of their first observations was that, with the onset of cold temperatures (from
73F to 39F), mice increase their food-seeking only after a delay of about six
hours, suggesting this behavioral change is not simply a direct result of cold
sensing.
Using techniques called whole-brain clearing and light sheet microscopy, the researchers compared the activity of neurons across the brain during cold versus warm conditions.
Soon they made a key observation: While most of the
neuronal activity across the brain was much lower in the cold condition,
portions of a region called the thalamus showed higher activation.
Eventually, the team zeroed in on a specific cluster of neurons called the xiphoid nucleus of the midline thalamus, showing that activity in these neurons spiked under cold conditions just before the mice stirred from their cold-induced torpor to look for food.
When less food was available at the onset of the cold condition,
the activity increase in the xiphoid nucleus was even greater—suggesting that
these neurons respond to a cold-induced energy deficit rather than cold itself.
When
the researchers artificially activated these neurons, the mice increased their
food-seeking, but not other activities. Similarly, when the team inhibited the
activity of these neurons, the mice decreased their food-seeking. These effects
appeared only under the cold condition, implying that cold temperatures provide
a separate signal that must also be present for appetite changes to occur.
In
a last set of experiments, the team showed that these xiphoid nucleus neurons
project to a brain region called the nucleus accumbens—an area long known for
its role in integrating reward and aversion signals to guide behavior,
including feeding behavior.
Ultimately,
these results may have clinical relevance, Ye says, for they suggest the
possibility of blocking the usual cold-induced appetite increase, allowing
relatively simple cold exposure regimens to drive weight loss much more
efficiently.
“One
of our key goals now is to figure out how to decouple the appetite increase
from the energy-expenditure increase,” he says. “We also want to find out if
this cold-induced appetite-increase mechanism is part of a broader mechanism
the body uses to compensate for extra energy expenditure, for example after
exercise.”
Reference:
“Xiphoid nucleus of the midline thalamus controls cold-induced food seeking” by
Neeraj K. Lal, Phuong Le, Samarth Aggarwal, Alan Zhang, Kristina Wang, Tianbo
Qi, Zhengyuan Pang, Dong Yang, Victoria Nudell, Gene W. Yeo, Alexander S. Banks
and Li Ye, 16 August 2023, Nature.
DOI: 10.1038/s41586-023-06430-9