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, February 19, 2020

Flickering Light Convinces Brain Proteins to Fight Alzheimer’s Disease

Did your stroke hospital and doctors going do one damn thing when this came out a year ago to see this gets tested in humans? Or will they sit with their heads up their asses sucking on their thumbs waiting for SOMEONE ELSE TO SOLVE THE PROBLEM? 

 

Flashing Light, Sound Restore Memory in Alzheimer's Mice Flashing Light, Sound Restore Memory in Alzheimer's Mice March 2019

 

Are you willing to try this even without human research? What is the downside?

The latest here which your stroke hospital will also ignore. Do you prefer your incompetency NOT KNOWING, or NOT DOING?

Flickering Light Convinces Brain Proteins to Fight Alzheimer’s Disease


Building upon a significant 2016 study that established a link between flickering light and Alzheimer’s treatment, researchers at Georgia Tech have now tapped into the brain chemistry behind the light’s effectiveness.
The original study, authored by Annabelle Singer when she was a professor at MIT, discovered that light flickering at 40 Hz entices brain immune cells—called microglia—to purge amyloid beta plaque, which have long been linked to the onset of Alzheimer’s Disease. The 40 Hz frequency stems from the observation that brains of Alzheimer's patients suffer early on from a lack of gamma, moments of gentle, constant brain waves that activate neuron activity. Its most common frequency is around 40 Hz—making that number the perfect target. (It’s worth nothing that, in an unrelated 2016 study, research connected gamma to working memory, a function key to train of thought.)
In the current study, Singer and colleagues in her Georgia Tech lab exposed healthy mice to light pulsing at 40 Hz and saw a surge of cytokines, accompanied by phosphoproteins. According to the researchers, the surging cytokines hinted at a connection with microglial activity, and in particular, the cytokine Macrophage Colony-Stimulating Factor (M-CSF). Since the phosphoproteins showed up first—about 15 minutes into the flickering of the light—the researchers hypothesize the proteins actually triggered the release of the cytokines at about the 1-hour mark.
“The vast majority of cytokines went up, some anti-inflammatory and some inflammatory, and it was a transient response,” said Georgia Tech’s Levi Wood, who co-led the study. “Often, a transient inflammatory response can promote pathogen clearance; it can promote repair.”
Interestingly, while the study was conducted on mice, the results are directly related to an undergoing human clinical trial at Emory University.
"I'll be running samples from mice in the lab, and around the same time, a colleague will be doing a strikingly similar analysis on patient fluid samples," said Kristie Garza, graduate research assistant in the Singer Lab and the study's first author.
In future studies, the researchers plan to look for a causal connection between a surge of cytokines and microglia activation. Additionally, based on results from stimuli intended as controls, the researchers may examine additional light frequencies—especially 20 Hz.
“At 20 Hz, cytokine levels were way down. That could be useful, too. There may be circumstances where you want to suppress cytokines,” said Singer. “We're thinking different kinds of stimulation could potentially become a platform of tools in a variety of contexts like Parkinson's or schizophrenia. Many neurological disorders are associated with immune response.”

No comments:

Post a Comment