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.

Friday, July 17, 2026

New images map key membrane protein in brain related to stroke

 Will your competent? doctor and hospital ENSURE FURTHER RESEARCH OCCURS?  Oh NO; you DON'T have a functioning stroke doctor or hospital, do you?

And all this earlier research COMPLETELY PROVING INCOMPETENCE since nothing was done!

New images map key membrane protein in brain related to stroke

Discovery could provide a blueprint for improved treatment of stroke

Peer-Reviewed Publication

Oregon Health & Science UniversitY

Scientists have for the first time mapped in exquisite, three-dimensional detail six major conformations of a membrane in the brain related to learning, memory and fear-related behavior.

The study, led by researchers at Oregon Health & Science University, published today in Nature Structural & Molecular Biology.

Researchers used state-of-the-art cryo-electron microscopy housed in OHSU’s South Waterfront Campus to capture the most detailed view yet of a specific type of membrane protein: an acid-sensing ion channel known as ASIC1a.

The findings could form the blueprint for drug development useful in treating stroke, said senior author Isabelle Baconguis, Ph.D., assistant professor in the OHSU Vollum Institute.

“Previous studies show that when you block this channel, it can be

neuroprotective

(Meaning stopping the the neuronal cascade of death in the first week! Neuroprotection is such a bland word, doesn't impart immediacy at all!) 

,” Baconguis said. “If you’re able to design a drug that infuses an inhibitor to this channel, it could lengthen the survival of the tissue in cases of stroke.”

Already, scientists in Australia are using a molecule derived from spider venom that explicitly targets ASIC1a to improve outcomes in heart attacks and stroke.

OHSU researchers used recombinant DNA technology to express the human gene to generate human proteins they imaged using cryo-EM. Because acid-sensing ion channels respond to variations of extracellular pH in the central and peripheral nervous systems, researchers were able to capture six distinct conformations by varying their exposure to acidity.

“In our bodies, there are locations where cells undergo different pH conditions, especially in the brain,” Baconguis said. “In neuronal injuries such as stroke, where brain tissue undergoes a drop in pH, these channels can be activated causing tissue damage.”

The images provide a blueprint for designing new drugs capable of inhibiting this one specific acid-sensing ion channel in cases of stroke.

“The sooner you can protect brain tissue from damage, the less severe disability stroke survivors will have,” Baconguis said. “Time is of the essence when it comes to stroke.”

In addition to Baconguis, co-authors include James Cahill, Kimberly A. Hartfield, Ph.D., Craig Yoshioka, Ph.D., of OHSU; Stephan Alexander Pless, Ph.D., Nadine Ritter, Ph.D., and Mette Homann Poulsen, Ph.D., of the University of Copenhagen; and Stephanie Andrea Heusser, Ph.D., of the University of Copenhagen in Denmark and Linköping University in Sweden.

The research was supported by the National Institutes of Health, grant award R24GM154185, RO1GM138862 from the National Institute of General Medical Sciences (NIGMS); and the Lundbeck Foundation, grant award R313-2019-571. Electron microscopy was performed at the Multiscale Microscopy Core, part of OHSU’s university-shared resource cores. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.


No comments:

Post a Comment