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 19, 2025

First-of-Its-Kind Stroke Recovery Drug Mimics Physical Rehabilitation

 Do you really think your incompetent doctor and hospital will ensure human testing gets done? Competence would mean this is already on their radar and they have plans in place RIGHT NOW! So, are they competent or not?

Haven't they been working on gamma oscillations for years now? NO? So, definitely no competence there at all?

gamma oscillations (13 posts to May 2012)

  • gamma oscillations (5 posts to May 2021)

    First-of-Its-Kind Stroke Recovery Drug Mimics Physical Rehabilitation

    Purple neurons against a black background with glowing circles on the synapses representing electrical signals.
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    A new study by UCLA Health has discovered what researchers say is the first drug to fully reproduce the effects of physical stroke rehabilitation in model mice, following from human studies.


    The findings, published in Nature Communications, tested two candidate drugs derived from their studies on the mechanism of the brain effects of rehabilitation, of which one resulted in significant recovery in movement control after stroke in the mouse model.


    Stroke is the leading cause of adult disability because most patients do not fully recover from the effects of stroke. There are no drugs in the field of stroke recovery, requiring stroke patients to undergo physical rehabilitation which has shown to be only modestly effective.


    “The goal is to have a medicine that stroke patients can take that produces the effects of rehabilitation,” said Dr. S. Thomas Carmichael, the study’s lead author and professor and chair of UCLA Neurology. “Rehabilitation after stroke is limited in its actual effects because most patients cannot sustain the rehab intensity needed for stroke recovery.

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    “Further, stroke recovery is not like most other fields of medicine, where drugs are available that treat the disease—such as cardiology, infectious disease or cancer,” Carmichael said. “Rehabilitation is a physical medicine approach that has been around for decades; we need to move rehabilitation into an era of molecular medicine.”


    In the study, Carmichael and his team sought to determine how physical rehabilitation improved brain function after a stroke and whether they could generate a drug that could produce these same effects.


    Working in laboratory mice models of stroke and with stroke patients, the UCLA researchers identified a loss of brain connections that stroke produces that are remote from the site of the stroke damage. Brain cells that are located at a distance from the stroke site get disconnected from other neurons. As a result, brain networks do not fire together for such things like movement and gait.


    The UCLA team found that some of the connections that are lost after stroke occur in a cell called a parvalbumin neuron. This type of neuron helps generate a brain rhythm, termed a gamma oscillation, which links neurons together so that they form coordinated networks to produce a behavior, such as movement. Stroke causes the brain to lose gamma oscillations. Successful rehabilitation in both laboratory mice and in humans brought gamma oscillations back into the brain, and in the mouse model, repaired the lost connections of parvalbumin neurons.


    Carmichael and team then identified two candidate drugs that might produce gamma oscillations after stroke. These drugs specifically work to excite parvalbumin neurons. The researchers found one of the drugs, DDL-920, developed in the UCLA lab of Dr. Varghese John, who coauthored the study, produced significant recovery in movement control.


    Further studies are needed to understand the safety and efficacy of this drug before it could be considered for human trials.


    Reference: Okabe N, Wei X, Abumeri F, et al. Parvalbumin interneurons regulate rehabilitation-induced functional recovery after stroke and identify a rehabilitation drug. Nat Commun. 2025;16(1):2556. doi: 10.1038/s41467-025-57860-0


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