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.”
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