Maybe this might fix two of the known problems in the neuronal cascade of death. I wonder what strategy is being followed.
1. glutamate poisoning
2. excitotoxicity
Found out this was tested in rats in 2004. This just shows you how fucking poor our stroke leadership and strategy is. 12 years to get to human testing That explains why I haven't written about it, it was before I had my stroke in 2006.
http://www.fau.edu/newsdesk/articles/stroke-treatment.php
A biomedical scientist in the Charles E. Schmidt
College of Medicine at Florida Atlantic University has received a $1.2
million grant from the James and Esther King Biomedical Research
Program, Florida Department of Health, to develop a new and innovative
approach to treat stroke.
Jang Yen (John) Wu, Ph.D., principal investigator and a
senior Schmidt fellow and distinguished professorof biomedical science
in FAU’s College of Medicine, will use a two-pronged approach to treat
stroke in the study. He will preserve and restore brain function by
protecting the brain against stroke induced injury, and also will
stimulate neurogenesis to replenish new brain cells using granulocyte
colony-stimulating factor (GCSF), an FDA-approved drug used to enhance
blood cellular development.
“Many drugs that are designed for stroke intervention
and treatment are based on their anti-oxidative properties or blockers
of calcium channels or glutamate receptors,” said Wu. “However, no
clinically effective therapeutic intervention for stroke has yet been
developed. Furthermore, no non-invasive in vivo procedure is available for monitoring the progression of the treatment for stroke.”
Wu and his collaborators will use gene therapy and a
unique non-invasive MRI monitoring system they developed to observe the
delivery and expression of GCSF, as well as the progression of ischemic
strokes using rodent models of the disease.
“Targeted MRI is highly sensitive and specific when
it is coupled with nanoparticles containing specific oligonucleotide
probes and can be used to track neural progenitor cells in vivo after
gene therapy or stem cell therapy in preclinical and perhaps even
clinical disease models,” said Wu. “Using targeted MRI we will be able
to evaluate the expression of trans genes and brain repair
non-invasively within a living organism.”
Wu anticipates that as a neuroprotectant can
potentially be a powerful growth factor because it is able to preserve
the central nervous system using several overlapping mechanisms that not
only activate cell survival pathways together with suppression of cell
death/apoptotic pathways, but also elicit neurogenesis and angiogenesis.
The Centers for Disease Control and Prevention
estimates that stroke kills almost 130,000 Americans each year, and on
average one American dies from a stroke every four minutes.
Approximately 87 percent of all strokes are ischemic strokes, when blood
flow to the brain is blocked. Stroke is the leading cause of serious
long-term disability and costs the U.S. an estimated $34 billion each
year for healthcare services, medications, and missed days of work.
“The short- and long-term impacts of having a stroke
can be devastating for the individual as well as his or her family,”
said Arthur J. Ross, III, M.D., M.B.A., interim dean and professor in
FAU’s College of Medicine. “We are extremely proud of Dr. Wu’s research
and we are very grateful for receiving this grant from the James and
Esther King Biomedical Research Program. With this grant, Dr. Wu will be
able to develop a novel way to potentially prevent and treat strokes
not only for Florida residents but world-wide.”
Use the labels in the right column to find what you want. Or you can go thru them one by one, there are only 28,983 posts. Searching is done in the search box in upper left corner. I blog on anything to do with stroke.DO NOT DO ANYTHING SUGGESTED HERE AS I AM NOT MEDICALLY TRAINED, YOUR DOCTOR IS, LISTEN TO THEM. BUT I BET THEY DON'T KNOW HOW TO GET YOU 100% RECOVERED. I DON'T EITHER, BUT HAVE PLENTY OF QUESTIONS FOR YOUR DOCTOR TO ANSWER.
Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.
What this blog is for:
My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.
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