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VA RESEARCH OFFERS NEW HOPE FOR STROKE
PATIENTS -- Scientists are looking to reverse
stroke
damage by jumpstarting the growth of nerve
fibers.

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Story here...
http://www.scienceda
ily.com/releases/2008/08/080825132115.htm
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New Hope For Stroke Patients: Reversing
Stroke Damage By Jumpstarting Growth Of Nerve Fibers
ScienceDaily — If a stroke patient doesn't get treatment within
approximately the first three hours of symptoms, there's not much doctors
can do to limit damage to the brain.
But now researchers report a technique that potentially could restore
functions to patients weeks or even months after a stroke. The technique
involves jumpstarting the growth of nerve fibers to compensate for brain
cells destroyed by the stroke.
"In the best-case scenario, this would open up the window of time that
people could recover and go back to normal functional status," said
Gwendolyn Kartje, MD, Ph.D., a professor in the department of cell
biology, neurobiology and anatomy and department of neurology at Loyola
University Chicago Stritch
School
of Medicine in Maywood, Ill. and chief of neuroscience research at Edward
Hines Jr. VA Hospital in Hines, Ill.
Kartje and colleagues described the experimental approach, called anti-nogo-A
immunotherapy, in a recent review article in the journal Topics in Stroke
Rehabilitation.
Anti-nogo has dramatically improved functions in lab animals that have
experienced strokes. And an ongoing clinical trial in Europe and Canada is
testing anti-nogo in humans who have suffered spinal cord injuries.
Most strokes are caused by clots that block blood flow to one part of the
brain, killing brain cells within hours. The drug TPA can minimize damage
by dissolving the clot. But TPA is safe and effective only when given
within about three hours of the onset of symptoms. Most patients don't
receive treatment within that brief window. Patients typically arrive at
the hospital too late, or hospitals do not begin administering TPA soon
enough.
Anti-nogo is among several new approaches under study that potentially
could reverse stroke damage, researchers wrote. Nogo-A is a protein that
inhibits the growth of nerve fibers called axons. It serves as a check on
runaway nerve growth that could cause a patient to be overly sensitive to
pain, or experience involuntary movements. (The protein is called nogo
because it in effect says to axons: "No go.") In anti nogo immunotherapy,
an antibody disables the nogo protein.
The left side of the brain controls movements on the right side of the
body, and vice versa. Thus, a stroke on the left side of the brain can
cause paralysis on the right side of the body. In such a patient, anti-nogo
would, it's hoped, spur the growth of axons from the healthy right side of
the brain. These axons would then grow into the right side of the body and
restore functions lost by the stroke.
Anti nogo has been tried on rats that have experienced strokes in old age.
As in people, strokes in rats affect one side of the body. Following
strokes, the rats were unable to pick up pellets of food with the front
paw on the affected side. After anti-nogo, function in this paw was almost
completely restored in some rats.
The Swiss pharmaceutical company Novartis is sponsoring a phase 1 clinical
trial of anti-nogo for patients paralyzed by spinal cord injuries. Kartje
believes anti-nogo also has great potential for stroke patients. A
clinical trial for stroke patients could begin as early as 2012, she said.
Loyola is among the potential sites for such a trial.
Anti nogo "offers the potential for stroke patients to recover, return to
nearly normal functional status, and stay out of nursing homes," Kartje
said. "Theoretically, there's no reason why this should not happen."
Kartje began studying the nogo protein in 1992, and has published numerous
papers on the topic. Her lab at Hines is funded by the Veterans
Administration, with additional funding from the National Institutes of
Health, Neuroscience Institute at Loyola University Chicago Stritch School
of Medicine, Falk Foundation and Illinois Regenerative Medicine Institute.
Adapted from materials provided by Loyola
University Health System.
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