A new study found evidence that shows how obesity affects the body on a metabolic level by disrupting mitochondrial function.
- Previous
research shows obesity can negatively impact a number of the body’s systems
and increase a person’s risk for several diseases.
- A
new study found evidence that shows how obesity affects the body on a
metabolic level by disrupting mitochondrial function.
- The
results could potentially pave the way for new obesity treatments and
prevention strategies.
Approximately 38% of the world’s population is considered obese or overweight,
according to the World Obesity Federation.
Researchers estimate the
majority of the global adult population will be either overweight or obese
by 2030.
Previous research shows obesity can negatively impact
a number of the body’s systems, including the respiratory, digestive, skeletal,
and muscular systems. It can also raise a person’s risk for
several diseases including:
- stroke
- high
blood pressure
- sleep
apnea
- certain types of cancer
Now researchers from the University of California —
San Diego report evidence that obesity also affects the body on a metabolic
level. Scientists believe this finding may lead to the development of new
therapies for the treatment or prevention of obesity.
The study was recently
published in the journal Nature
Metabolism.
Metabolic changes
caused by obesity
Obesity is defined as
accumulating too much body fat within
the white adipose tissue of the body.
Previous studies show that obesity causes metabolic
changes within the white adipose tissue causing:
- inflammation
- insulin
resistance
- hormone
issues
- apoptosis (cell death)
Lead study author Dr. Alan Saltiel, professor in the Department of Medicine at the University of
California — San Diego School of Medicine, told Medical News Today his
lab has been working for 40 years to understand hormones like insulin control and
where and when energy is stored or used.
“Obesity has a major
impact on how well these hormones do their job, and vice versa,” Dr. Saltiel
said.
“In
the last few years, we’ve turned our attention to the ways that fat and liver
cells adapt to conditions associated with overeating when the cells are flooded
with nutrients. The interesting thing is that these cells become more efficient
at storing energy and less efficient at burning it, which is one reason why it
is so hard to lose weight,” he continued. “We’ve been exploring the underlying
molecular changes that explain this.”— Dr. Alan Saltiel, lead study author
Mitochondrial
dysfunction in obesity
Dr. Saltiel explained
that obesity causes metabolic abnormalities in the body because the body has to manage
excessive amounts of energy due to the condition.
In other words, the body
has to find a way to store energy or excess calories since there is a limit on
how much can be burned off.
“Thus, adjustments are
made, and this change in mitochondrial structure and function is one that we
highlight in this paper,” he added.
Using a mouse model, Dr.
Saltiel and his team found when mice were fed a high fat diet, the mitochondria — known as
the “powerhouse of the cell” — within fat cells fragmented into smaller
mitochondria. Researchers found these smaller mitochondria could not burn as
much fat as when the larger mitochondria were all together.
“In the normal,
non-obese state, mitochondria maintain their health through a cycle of
continual fusion and fission, which means they break apart and reform,” Dr.
Saltiel explained. “We found that the changes that occur in obesity tip the
scales so that mitochondria break apart more — the process known as fission.”
The researchers also
discovered that these changes only occur in one type of fat cells — the kind
found below the skin (subcutaneous) that is mainly in the hips and thighs.
“This is thought
to be the good adipose depot, as it has the potential to burn as well as store
fat,” Dr. Saltiel said.
“We found that
mitochondria are normally longer and more active in this fat depot compared to
the adipose tissue found in the midsection — called visceral fat — but
obesity causes excessive mitochondrial fission in subcutaneous fat, so it looks more like visceral fat and loses its ability to burn fat,”
he noted.
Turning off the metabolism-disrupting molecule
During their research,
Dr. Saltiel and his team discovered this fragmentation of mitochondria was
caused by a single molecule called RaIA.
“We’ve been studying the
role of RalA in the actions of insulin for a long time,” Dr. Saltiel said.
“We were surprised to
discover that RalA is a master regulator of mitochondrial fission, and when it
is chronically activated in obesity, it tips the scales toward fission.”
When scientists deleted
the gene associated with the RaIA molecule in mice, they were able to protect
them from weight gain from a high-fat diet.
Researchers believe this
finding could potentially lead to new ways of preventing and/or treating
obesity.
“I think the
primary finding here is that there is mitochondrial dysfunction produced by
obesity through this RalA-dependent pathway,” Dr. Saltiel explained.
“It is possible that
there are new drug targets in the pathway that may allow us to reverse the
excessive mitochondrial fission and thus increase fat burning. But this is a
long way off, and who knows what other important processes are controlled by
this pathway in the body,” he added.
Thinking about weight loss on a cellular level
MNT also spoke with Dr. Mir Ali,
bariatric surgeon and medical director of MemorialCare Surgical Weight Loss
Center at Orange Coast Medical Center in Fountain Valley, CA, about this study.
Dr. Ali said he thought
the research was very interesting as it showed how obesity is adversely
affecting the body even at a cellular level.
“I think most people
understand that obesity is detrimental to their health, but to see this go down
to the cellular level makes it even more impactful, I think,” he continued. “I
think that if more people understand how widely impactful obesity is on the
body, it will motivate some people to do something about it.”
Dr. Ali said the
study findings that show how obesity affects the mitochondria could lead to the
development of medication that could block that effect and have a role in
fighting obesity.
“This is very early
research — it’s going to require a lot more work finding something that can
block these kinds of effects on the cellular level,” Dr. Ali added. “It’s going
to take a lot of work, but it’s encouraging that there’s something we can do at
that level.”
https://www.medicalnewstoday.com/articles/obesity-caused-by-metabolism-disrupting-molecule
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