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, July 31, 2025

UCSF discovery points to new strategies for Alzheimer's treatment

Do you really think your competent? doctor and hospital will ensure further research creates an intervention before your children and grandchildren need it? I doubt it.

 Google 'how to test for ADGRG1' to bring to your doctor.

 UCSF discovery points to new strategies for Alzheimer's treatment


UCSF scientists have discovered how microglia engulf and break down amyloid beta, a protein that builds up in Alzheimer's, with devastating consequences for the brain. 

In Alzheimer's disease, proteins like amyloid beta form clumps, known as plaques, that damage the brain. 

But in some people, immune cells called microglia break down these proteins before they can cause harm. This leads to fewer and smaller clumps - and much milder symptoms.

Researchers at UC San Francisco identified a molecular receptor that enables microglia to gobble up and digest amyloid beta plaques. 

Without the receptor, ADGRG1, the microglia barely nibbled on the toxic protein. Using a mouse model of Alzheimer's disease, the researchers observed how the loss of ADGRG1 led to the rapid buildup of amyloid plaques, neurodegeneration, and problems with learning and memory.

"We think this receptor helps microglia do their job of keeping the brain healthy over many years."

Xianhua Piao, MD, PhD, Physician-Scientist, Department of Pediatrics, University of California - San Francisco

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Indeed, when the researchers reanalyzed a prior study of gene expression in the human brain, they found that individuals who died of mild Alzheimer's had microglia with abundant ADGRG1, and mild cognitive impairment - implying that the microglia ate well and kept the disease in check. But in those who died of severe Alzheimer's, the microglia had very little ADGRG1, and the plaques proliferated.

ADGRG1 is one of hundreds of G protein-coupled receptors, which are routinely targeted in drug development. This bodes well for a rapid translation of the discovery into new therapies.

"Some people are lucky to have responsible microglia," Piao said. "But this discovery creates an opportunity to develop drugs to make microglia effective against amyloid-beta in everyone."

Source:
Journal references:

Zhu, B., et al. (2025). G-protein-coupled receptor ADGRG1 drives a protective microglial state in Alzheimer's disease through MYC activation. Neurondoi.org/10.1016/j.neuron.2025.06.020 

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