Last Updated: 2003-05-30 11:31:56 -0400 (Reuters Health)
LONDON (Reuters Health) - A type of protein that helps cells respond to heat,
cold and other environmental stresses could one day be used to slow down
degenerative brain diseases like Alzheimer's, Parkinson's and Huntington's,
British researchers said on Friday.
Early research suggests that so-called heat shock proteins could also help
against conditions such as motor neurone disease and stroke damage, said
Professor Jacqueline de Belleroche from Imperial College London.
"At present, there is no cure for neuro-degenerative diseases, such as
Alzheimer's and Parkinson's, but the discovery of the beneficial effects of this
protein in the brain may provide us with a way to at least slow down the disease
process," she said.
In the Journal of Biological Chemistry, de Belleroche and colleagues report
that the naturally occurring heat shock protein Hsp27 was able to reduce brain
cell death in animal experiments.
Mice engineered to have high levels of the protein throughout the brain,
spinal cord and other tissues had lower rates of death and brain cell death
after they were injected with a toxic substance that damages cells. The
protective effect was seen in the hippocampus, a part of the brain affected by
neurological diseases.
In earlier studies, the researchers achieved similar results when they
injected Hsp27 directly into the brain.
"Although this is unlikely to provide a cure for neuro-degenerative
disorders, it could be vital in slowing their progress," de Belleroche said.
"Eventually it may be possible to use a drug to increase levels of Hsp27 in the
brain which could be given to those suffering from neuro-degenerative diseases."
All cells contain a range of heat shock proteins and the proteins are
produced in response to environmental stresses like heat, cold and low oxygen
levels. Under normal conditions they act like "chaperones" to make sure a cell's
proteins are in the right place and shape at the right time.
"It's one of the systems we think is a natural defence system," de Belleroche
told Reuters Health. "We're looking at trying to boost the natural system and
hopefully translate it into treatment."
The heat shock proteins might achieve their effects by stopping the buildup
of solid structures or aggregates within brain cells, a process that
characteristically triggers cell death in neuro-degenerative diseases, she said.
"What this and other heat shock proteins do ... is stop those insoluble
aggregates (from) forming, and they help to re-fold the protein so it can arrest
the process."
The next step is to pin-point exactly when the heat shock protein acts in the
chain-reaction of events leading to cell death, and develop drugs to affect that
process, she said.
"It's a line that we're hoping to pursue," de Belleroche said. "We're testing
out a few compounds but we haven't got any results yet."
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