Where fat comes from determines whether the body
can metabolize it effectively. Researchers at Washington
University School of Medicine in St. Louis have found
that the "old" fat stored in the body's peripheral
tissues -- that is, around the belly, thighs or bottom
-- can't be burned efficiently unless "new" fat is
eaten in the diet or made in the liver.
The research team developed genetically engineered
mice missing an important fat synthesizing enzyme
in the liver. As a result, the mice, called FASKOL
mice (Fatty Acid Synthase KnockOut in Liver), could
not produce new fatty acids in the liver. Because
liver fatty acids are vital for maintaining normal
sugar, fat and cholesterol metabolism, these mice
must take in dietary fat to remain healthy.
Reporting in the May issue of the journal Cell Metabolism,
the researchers say these mice developed fatty liver
disease when placed on a zero fat diet.
"When we took dietary fat away from the FASKOL mice,
their livers quickly filled with fat," says senior
investigator Clay F. Semenkovich, M.D., professor
of medicine and of cell biology and physiology. "Their
'old' fat stores mobilized to the liver, but their
livers could not initiate fat burning, and the fat
just accumulated. We concluded that to regulate fat
burning, the liver needs 'new' fat."
New fat is the fat that is consumed in food or is
newly made in the liver as glucose is converted to
fat by fatty acid synthase, the enzyme missing in
the FASKOL mice. When the system takes in high amounts
of glucose, fatty acid synthase in the liver makes
it into new fat.
In addition to fatty livers, the transgenic mice
developed low blood sugar levels on the zero fat diet.
Both symptoms were reversed with dietary fat, and
in fact on a normal diet, the transgenic mice were
no different than normal mice in terms of body weight,
body fat, metabolic rate and food intake.
The effect of added dietary fat was duplicated when
the mice were treated with a drug that activates a
protein called PPAR-alpha. Liver fat declined to normal
in the FASKOL mice within 10 days of receiving the
PPAR-alpha activating drug.
PPAR-alpha is a protein found in all mammals and
is central to metabolic processes that extract energy
from dietary components like carbohydrates and fats.
Because the PPAR-alpha activating drug did the same
work that dietary fat does, the investigators concluded
that new fat may be crucial to initiating the PPAR-alpha
pathway.
"Scientists have argued that PPAR-alpha is activated
by fats," says Semenkovich, who also directs the Division
of Endocrinology, Metabolism and Lipid Research and
is a staff physician at Barnes-Jewish Hospital. "But
we've never known which fats or where they come from.
This study suggests that new fat is a 'key' that unlocks
the 'door' for PPAR-alpha in the liver."
The liver is very important for processing nutrients
consumed in the diet and sending them on to the rest
of the body. Abnormal processing of glucose or lipids
in the liver contributes to problems of type 2 diabetes
and atherosclerosis, and fatty liver disease often
is seen in people who are obese or suffer from insulin
resistance.
"There's also good evidence that the liver plays
a key role in mediating cardiovascular risk through
the secretion of multiple proteins associated with
inflammation," Semenkovich says. "In these mice we
found that when too much fat got into the liver, there
was excessive inflammation."
With Manu Chakravarthy, M.D., Ph.D., an endocrinology
fellow and first author of the paper, Semenkovich
found that new fat seems to solve those problems.
The research team is now trying to identify fats
that could be given in small amounts to activate the
PPAR-alpha pathway. They also are studying liver cells
and fat cells to see how the liver can tell the difference
between old fat and new fat.
Eventually, Semenkovich believes these findings could
lead to more effective strategies for the treatment
of obesity, type 2 diabetes and other metabolic problems.
For now, he says that dieters who want to lose fat
stored in peripheral tissues may find it useful to
take in small amounts of dietary fats, such as fish
oils, that might more effectively activate PPAR-alpha
and fat burning pathways through the liver.