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.

Wednesday, March 7, 2012

Biochemical Switch Linked To Stroke And Heart Disease - How It Turns On

How many researchers should be jumping on this to find out how to turn this into a prevention therapy?
http://www.medicalnewstoday.com/articles/242615.php
The science journal Proceedings of the National Academy of Sciences , has reported that scientists from the University of Leicester and Cardiff University have achieved a breakthrough in understanding how a 'biochemical switch', known as P2X1, which is associated with strokes and heart disease is 'turned on'.

Professor Richard Evans of the University of Leicester's Department of Cell Physiology & Pharmacology, who led the research explained:

"P2X1 receptors are protein molecules expressed on blood platelets which are cells involved in blood clotting. Drugs that block these receptors have the potential to reduce "dangerous" blood clotting that leads to strokes and heart attacks. Our research has looked at how the P2X1 receptor is "turned on". By biochemical studies and purifying the P2X1 receptor and using an electron microscope we have 'visualized' the receptor and detected changes in its shape when it is activated.

The P2X1 receptor is made of three identical parts and we have shown that activation leads to these twisting against each other. We found that if we chemically locked the receptor to stop this twisting, then the P2X1 receptor could not be fully activated. This is important as it gives the first realistic insight into how these novel receptors are turned on."


Evans concluded saying:

"This work will help to develop drugs that can stop the P2X1 receptor being "turned on" and would be useful to prevent stroke and heart attack."

No comments:

Post a Comment