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Omega-3 fatty acid
may prevent Alzheimer's disease and slow its
progression |
A diet high
in the omega-3 fatty acid DHA helps protect the brain
against the memory loss and cell damage caused by
Alzheimer's disease.
Neuroscientists from the University of California have shown
for the first time that a diet rich in DHA may lower the
risk of developing Alzheimer's disease and may help slow
progression of the disorder in its later stages.
Senior author
and Professor of Neurology, Greg Cole PhD, at the David
Geffen School of Medicine at UCLA explains "This is the
first proof that our diets affect how our brain cells
communicate with each other under the duress of Alzheimer's
disease. We saw that a diet rich in DHA, or docosahexaenoic
acid, dramatically reduces the impact of the Alzheimer's
gene."
He added that
the average person can easily add more omega 3 to the diet,
in the form of fish oil capsules, high-fat fish, or eggs
which have been supplemented with DHA.
The researchers focused on
Alzheimer's damage to synapses – the chemical connections
between brain cells that enable memory and learning.
They used mice which had
been bred with genetic mutations that cause the brain
lesions linked to advanced Alzheimer's disease. When they
found that the mice developed the lesions, but showed
minimal memory loss or synaptic brain damage, which might
normally have been expected, the scientists took a closer
look at the animals' diet.
They discovered that the
mice lived on a nutritious diet of soy and fish – two
ingredients rich in omega-3 fatty acids.
Because earlier studies had
suggested that omega-3 fatty acids might prevent Alzheimer's
disease, the researchers realised that the mice's diet could
be helping to fight the progression of brain damage.
To check whether this was
indeed happening, the scientists swapped safflower oil for
the soy and fish to create an unhealthy diet depleted of
omega-3 fatty acids. The mice were divided into two sets of
older mice, which already showed brain lesions but showed no
major loss of brain-cell activity. Both sets of mice were
given safflower oil, which is not high in DHA, instead of
the fish and soy diet. The second group were also given DHA
supplements from algae.
After five months, the
researchers compared each set of mice to a control group
that consumed the same diet but did not carry the
Alzheimer's genes. The results surprised them.
They found that the mice
who were given diets low in DHA had high levels of synaptic
damage in their brains, and they observed that these changes
closely resembled those in the brains of humans with
Alzheimer's disease.
Although the mice on the
DHA-supplemented diet also carried the Alzheimer's genes,
they still performed much better in memory testing than the
mice in the first group.
Even after adjusting for
all possible variables, DHA was the only factor remaining
that protected the mice against the synaptic damage and
memory loss that should have resulted from their Alzheimer's
genes, according to Professor Cole.
He said "We concluded that
the DHA-enriched diet was holding their genetic disease at
bay."
The UCLA scientists hope to
use their findings in a new study which will track DHA-related
biomarkers in the urine and cerebral spinal fluid of
Alzheimer's patients. Finding these biomarkers earlier would
enable treatment to begin earlier.
DHA is absorbed very
quickly by the human brain, and is critical for proper
cognitive function, eye development and mental tasks. DHA
helps keep the brain membrane fluid, moves proteins and
helps to convert signals from other parts of the body into
action.
Inexpensive sources of DHA
include coldwater fish, such as salmon, halibut, mackerel,
sardines and herring. These fish consume algae, which is
high in DHA.
However, these fish also
absorb more mercury, dioxin, PCP and other metals and
therefore a less risky strategy is to consume either fish
oil or purified DHA supplements made from algae.
Alternatively DHA-rich eggs laid by chickens that eat DHA-supplemented
feed can be included in the diet.
This study was funded by
The National Institute on Aging, National Institute of
Neurological Diseases and Stroke, and Canadian Institutes of
Health Research.
Source: EurekAlert
September 1, 2004
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