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.

Thursday, March 14, 2019

New approach to stroke treatment could minimize brain damage

I bet nothing will be done with this, just like nothing is being done for the other causes of the neuronal cascade of death. 


1.  glutamate poisoning   March 2012
2.  excitotoxicity April 2012
3.  Capillaries that don't open due to pericytes  Sept. 2011
4.  Inflammatory action leaking through the blood brain barrier.
http://link.springer.com/article/10.1007/s12975-013-0301-2  May 2013

5.  Lysosomal Membrane Permeabilization as a Key Player in Brain Ischemic Cell Death: a “Lysosomocentric” Hypothesis for Ischemic Brain Damage Nov. 2013

Notice how long ago all this research was published. Why is your stroke hospital president still president and the board of directors still there?  I would have all of them fired for cause.

New approach to stroke treatment could minimize brain damage

A new treatment for a common type of stroke may soon be possible, thanks to a discovery by an international team of researchers led by the University of British Columbia.
In a study published today in the Journal of Experimental Medicine, researchers successfully used a new approach that significantly minimized brain damage caused by stroke in mouse models. The new approach works by targeting hemichannels—pathways that allow for the flow of chemical ions and small molecules—that are expressed by astrocytes, cells that play a protective role for neurons in the brain.
When stroke occurs, these hemichannels open and can leak toxic molecules into the space outside the astrocytes, causing inflammation and damage to neurons.
“Our study definitively confirms that hemichannels are detrimental in stroke, and that we can block them to minimize damage to the brain,” said lead author Moises Freitas-Andrade, who conducted this study as a postdoctoral research fellow at UBC and currently is a research fellow at The Ottawa Hospital Research Institute. “It’s a different approach to stroke treatment. A lot of previous research has focused on trying to protect neurons, but here we sought a way to enhance the astrocyte’s ability to protect neurons in stroke.”
The researchers focused specifically on ischemic strokes, which occur when the arteries to the brain become narrowed or blocked, resulting in severely reduced blood flow. Ischemic stroke is the most common type, accounting for about 80 per cent of all strokes, according to the Heart and Stroke Foundation of Canada.
For the study, the researchers used a genetic approach that mutated the channel proteins, called connexins, in such a way that blocks the formation of hemichannels. This allows the astrocytes to protect the neurons, significantly reducing the size of the stroke injury in the brain. The researchers also used a molecule called Gap19 to block the hemichannels, in the same stroke model, which also resulted in smaller stroke damage. Together, the two approaches demonstrate that connexin hemichannel blockers could be used as a neuroprotective agent in stroke.
The researchers also attempted to mimic “real life” stroke conditions in the study, waiting two hours after the stroke occurred before administering the drug.
“It was important for us that we used a clinically realistic treatment window, especially if we were testing a drug that could potentially be used for treatment one day,” said the study’s senior author Christian Naus, professor emeritus in UBC’s department of cellular and physiological sciences, member of the Life Sciences Institute and an associate of the Djavad Mowafaghian Centre for Brain Health at UBC. “For the average person who has a stroke, two hours could easily elapse by the time paramedics arrive and the patient is taken to hospital and starts receiving treatment. This sets the stage for a combined approach where one could not only directly treat neurons in stroke, but could also enhance the astrocytes’ ability to protect neurons under stroke conditions.”
The researchers believe the approach could also have potential use for treating other neurodegenerative conditions such as traumatic brain injury and Alzheimer’s disease.
The study also involved researchers at the Fred Hutchinson Cancer Research Centre in Seattle and Ghent University in Belgium.
“This research is a great example of how the expertise from laboratories from three different countries could not only identify the importance of these connexin hemichannels but also discover the mechanisms involved and even identify possible avenues for treatment,” said study co-author Paul Lampe of the Fred Hutchinson Cancer Research Centre.
“Through the efforts of several labs, we were able to conduct in-depth explorations of channel protein function and its effect on disease treatment and outcome,” added Luc Leybaert of Ghent University.
This research was supported by grants from the Heart and Stroke Foundation of Canada, the Canadian Institutes of Health Research, the Canada Research Chairs program, the U.S. National Institutes of Health, the Fund for Scientific Research Flanders, the Interuniversity Attraction Poles Program, and the Geneeskundige Stichting Koningin Elisabeth.

Contact

Thandi Fletcher
UBC Media Relations
Tel: 604-822-2234
Cel: 604-868-0896
Email: thandi.fletcher@ubc.ca

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