'Browning' white fat helps treat obesity
By ANI
From
London (ANI): By manipulating the metabolic pathways in the body responsible
for converting vitamin A, retinol, into retinoic acid, a team of researchers
have discovered a way to turn foe to friend by essentially making white fat
take on characteristics of brown fat.
Brown
seems to be the colour of choice when it comes to the types of fat cells in our
bodies. Brown fat expends energy, while its counterpart, white fat stores it.
The
danger in white fat cells, along with the increased risk for diabetes and heart
disease it poses, seems especially linked to visceral fat. Visceral fat is the
build-up of fat around the organs in the belly.
So in
the battle against obesity, brown fat appears to be our friend and white fat
our foe.
The
findings, by researchers led by Jorge Plutzky from Women's Hospital (BWH) and
Harvard Medical School, put medical science a step closer in the race to
develop novel anti-obesity therapies.
Retinoids,
which are molecules derived from vitamin A metabolism, are responsible for many
biological functions. One such function is the control of fat cell development
and actions.
A key
step in retinoid metabolism occurs with help from an enzyme called
retinaldehyde dehydrogenase 1, or Aldh1a1. The researchers saw that in humans
and mice, Aldh1a1 is abundant in white fat cells, especially in the more
dangerous visceral fat (sometimes referred to as abdominal fat or belly fat).
When
Aldh1a1 was inhibited in white fat cells, those cells began acting like brown
fat cells. One of the defining characteristics of brown fat is its ability to
release energy as heat. Mice with either deficiency or inhibition of Aldh1a1
become protected against exposure to cold.
The
researchers saw this classic indicator of brown fat and its ability to generate
heat by oxidizing fat
(a chemical reaction involving oxygen) in their research.
Especially
exciting for the prospects of targeting Aldh1a1 for therapeutic benefit, the
researchers found that knocking down expression of the Aldh1a1 gene by
injecting antisense molecules into mice made fat by diet resulted in less
visceral fat, less weight gain, lower glucose levels, and protection against
cold exposure as compared to control mice.
"Brown
fat, and mechanisms that might allow white fat to take on brown fat
characteristics, has been receiving increasing attention as a possible way to
treat obesity and its complications," Plutzky said.
"Although
more work is needed, we can add specific aspects of retinoid metabolism to
those factors that appear involved in determining white versus brown fat,"
Plutzky added.
The
study has been published in online in Nature Medicine. (ANI)
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