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SKELETAL SYSTEM AND DIABETES |
Bones play important role in
regulating blood sugar, shows study
16 August, 2007:
In a discovery that may be
described as very surprising, an
international team of scientists has
found that bone plays an important
role in controlling sugar metabolism,
energy balance, and weight.
The finding, which suggests that the
skeleton is actually a member of the
endocrine system, adds immensely to
the understanding of metabolism and
may lead to new ways to prevent and
treat Type 2 diabetes.
The study – published in the August
10, 2007, issue of the journal Cell –
was carried out on laboratory mice by
researchers in New York, Chicago and
Hershey, Pennsylvania (the United
States), Seoul (Korea), Lyon (France),
Cambridge (the United Kingdom) and
Montreal (Canada).
It is generally believed that the
skeleton is an inert calcified
structure that just stops the body
from collapsing inside the skin.
Dr Gerard Karsenty and Paul Marks at
Columbia University Medical Center,
main authors of the paper, said: “The
discovery that our bones are
responsible for regulating blood sugar
in ways that were not known before
completely changes our understanding
of the function of the skeleton and
uncovers a crucial aspect of energy
metabolism.”
Karsenty and colleagues had suspected
that bone might be involved in
metabolism because leptin, a hormone
released by fat cells, is also
involved in the control of bone
formation. So they decided to look for
other molecules that might be
communicating between bone-forming
cells and the endocrine system.
Using laboratory mice, they discovered
metabolic processes, previously
unknown, where a hormone called
osteocalcin – that is known to
regulate mineralisation and is
released in bone-forming cells known
as osteoblasts – also regulates
glucose (blood sugar) and the
deposition of fat.
The scientists showed that an increase
in osteocalcin effectively prevents
the development of Type 2 diabetes and
obesity in the laboratory mice.
The finding is exciting because it
suggests that increasing the levels of
osteocalcin in patients with Type 2
diabetes could be a promising
treatment route, especially since such
patients tend to have low levels of
the hormone.
Osteocalcin was thought only to be
involved in bone development, but it
seems it has a second crucial role in
the endocrine system, that is,
increasing the secretion of insulin
and also increasing sensitivity to
insulin. Osteocalcin also boosts
production of pancreatic beta cells
that make insulin (a much sought but
currently unattainable path in new
treatment research for Type 2
diabetes) and reduces fat deposits by
interacting with fat cells.
When mice that did not have
osteocalcin were examined, it was
found that they had Type 2 diabetes,
an increase in fat deposits, a
decrease in insulin, a decrease in
adiponectin expression (a protein that
regulates fat deposits), and a much
lower count of beta cells in the
pancreas.
It came as a complete surprise to the
research team to discover that
endocrine processes in the pancreas
and fat cells were also being
controlled by signals from the
skeleton.
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