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.

Tuesday, April 14, 2015

MTfp-­siRNA reduces blood vessel infarct, improves overall brain activity in ischemic stroke model

How many decades is this going to take to get it proven in humans? I'm betting 100 years because we have shit for brains in our stroke associations with NO strategy and no way to solve any of the problems in stroke.
http://www.news-medical.net/news/20150319/MTfp-c2adsiRNA-reduces-blood-vessel-infarct-improves-overall-brain-activity-in-ischemic-stroke-model.aspx
BIOASIS TECHNOLOGIES INC. (OTCQX:BIOAF; TSX.V:BTI), a pioneering biopharmaceutical company focused on overcoming the limitations of therapeutic drug delivery across the blood-­‐brain barrier (BBB), announces the results from an animal ischemic stroke model performed at the National Research Council Canada with the biOasis Transcend carrier peptide, MTfp and siRNA (MTfp-­‐siRNA). Two key therapeutic effects were shown with MTfp-­‐siRNA; A high degree of reduction of the area of blood vessel infarct and improvement of overall brain activity as determined by neurological scoring.
On July 25th, 2014, biOasis announced that its newly discovered carrier peptide (MTfp), part of the biOasis Transcend family of carrier technologies, effectively delivered siRNA across the BBB and into brain cells. The company also announced that it achieved the goal of silencing the expression of a selected target gene in the brain by approximately 50%. This study prompted the company to move to a model of disease where therapeutic effects could be measured.
Ischemic stroke is the most common type of stroke in humans and an animal model that mimics stroke was chosen to establish the effectiveness of MTfp-­‐siRNA treatment administered immediately prior to induction of ischemic stroke.
Key Findings of Ischemic Stroke Model Treated with MTfp-­‐siRNA:
(1) The area of infarct (damage) was highly reduced in the animals treated with MTfp-­‐siRNA. Brain images revealed significantly less stroke damage in brain sections from animals treated with the MTfp-­‐siRNA when compared to the same brain regions in the control animals. The brain section images may be viewed below. The images show that there is more stroke damage (white areas) in the five sections from control animals (Left Panel) when compared to the same brain regions in the animals with stroke treated with the MTfp-­‐siRNA (Right Panel).
(2) Thirty-­‐minutes after induction of stroke, the neurological scores of the animals treated with the MTfp-­‐siRNA were significantly better than those of control animals. At 24 hours, controls animals demonstrated a slight improvement in neurological scores while MTfp-­‐siRNA treated animals showed a vast improvement and exhibited nearly normal neurological scores.
“The results clearly demonstrate that in an established animal model of stroke, therapeutic levels of siRNA that down-­‐regulate the expression of a key pathogenic gene were successfully delivered by MTfp to the brain, resulting in a significant reduction of infarct damage and improvement of neurological scores associated with healthy brain function,” said Dr. Wilfred Jefferies, biOasis Founding Scientist.

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