Potential to prevent loss of insulin in Type 2 diabetes
There are two completely different diseases known as diabetes. Type
1 is an autoimmune condition that often starts in childhood or
adolescence. Type 2 is a metabolic disorder sometimes associated with
lifestyle. In both cases, the insulin-secreting beta cells in the
pancreas die, albeit at different rates.
Until now, it was thought that the processes leading to beta cell death
were similar in both diseases. Scientists at the Garvan Institute of
Medical Research in Sydney have now shown that the causes of cell death
are quite different.
In April 2007, Garvan's Associate Professor Trevor Biden and Dr Ross
Laybutt published a landmark
paper establishing the existence of ER (Endoplasmic Reticulum)
stress in people with Type 2 diabetes. The ER is the part of a cell
where simple strings of amino acids are structured into
three-dimensional proteins which then go on to perform specific tasks
in the body. Insulin is one such protein. When the correct
re-structuring of proteins is disrupted, beta cells suffer ER stress,
and eventually die.
The new study, undertaken by PhD student Mia Akerfeldt, expands our
knowledge about ER stress in Type 2 diabetes, while ruling out its
importance in Type 1 diabetes. The paper is now online in the
international journal
Diabetes.
Mia is hopeful that the findings will translate quickly into
treatments. "Garvan was first to show that ER stress was present in
people with Type 2 diabetes, and that reducing it could slow down beta
cell death," she said. "We've not only shown the same thing again,
we've identified a potentially useful therapeutic agent."
Project leader Ross Laybutt echoes Mia's optimism. "One interesting
aspect of the new study is that we used a "chemical chaperone", an
agent that helps the secretory protein, in this case insulin, to form
properly. This compound relieved cell death and ER stress in laboratory
experiments."
"The compound, known as PBA, is already FDA approved for use in another
clinical application. That suggests it could be fast tracked for use in
humans to prevent or delay beta cell dysfunction."
"A study conducted in the United States demonstrated that this compound
cures diabetes in animals. The next step would be to conduct clinical
trials on people."
ABOUT GARVAN
The Garvan Institute of Medical Research was founded in 1963.
Initially a research department of St Vincent's Hospital in Sydney, it
is now one of Australia's largest medical research institutions with
approximately 400 scientists, students and support staff. Garvan’s main
research programs are: Cancer, Diabetes & Obesity, Immunology and
Inflammation, Bone, and Neuroscience. The Garvan’s mission is to make
significant contributions to medical science that will change the
directions of science and medicine and have major impacts on human
health. The outcome of Garvan’s discoveries is the development of
better methods of diagnosis, treatment, and ultimately, prevention of
disease.
All media enquiries should be directed to:
Alison Heather 02 9295 8128 or Jackie Crossman on 0402 218 662


