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, November 6, 2015

Reprogramming Neurons

And if we had  a stroke strategy we could send our doctors after this to create a stroke protocol for our rehabilitation use. But we don't so survivors are fucking screwed because no one is solving all the problems in stroke or following any stroke strategy at all. FUCKING HEY!!!
http://neurosciencenews.com/neuron-rewiring-neuroscience-3007/
Building on earlier work in which they disproved neurobiology dogma by “reprogramming” neurons — turning one form of neuron into another — in the brains of living animals, Harvard Stem Cell Institute researchers have now shown that the networks of communication among reprogrammed neurons and their neighbors can also be changed, or “rewired.”
The finding, by Paola Arlotta, a professor of stem cell and regenerative biology, in close collaboration with Takao Hensch, a professor of molecular and cellular biology, has implications for both a basic understanding of how neurons choose their synaptic partners when circuits wire during early development, and for developing strategies to change defective communication in psychiatric and neurodevelopmental diseases, such as schizophrenia and autism.
“What we’ve shown here is that not only neurons can be dramatically changed from one type into another from within the brain,” said Arlotta, who is also an associate member of the Stanley Center for Psychiatric Disease at the Broad Institute of Harvard and M.I.T., but also that “neighboring neurons recognize the reprogrammed cells as different and adapt by changing how they communicate with them.”
The work is published in the latest edition of the journal Neuron.
Graduate students Mohammed A. Mostajo-Radji and Zhanlei Ye, the first authors on the study, worked together to first reprogram neurons of the cerebral cortex that normally would connect the two sides of the brain into neurons that instead connect far away, for example in the spinal cord. They then monitored the behavior of a third class of cells, the local inhibitory interneurons, and showed that they change their synaptic connections onto the reprogrammed neurons. “Inhibitory neurons play pivotal roles in controlling the function and plasticity of local circuits in the cerebral cortex,” said Hensch.
“Transformed neurons were recognized as ‘new’ cells, with different properties, by neighboring inhibitory interneurons, which in turn created new circuitry appropriate for their ‘new’ neuronal target,” Arlotta said.
The neuroscientist said that the recent work demonstrates that “synaptic connections among neurons are not made randomly. The brain is much more sophisticated, and different neurons have ways to control the behavior of neighboring circuits in their own unique way to ultimately change how much inhibition, for example, they receive from their synaptic partners.”
The results are important for defining the rules by which neurons in the brain are wired in the first place, but also may provide a way to understand how to rewire the brain in the context of a malfunctioning, pathological circuit. In other words, she said, “Our work shows that, as a neuron, it is important to know who you are, as that will tell your neighbors how to talk with you.
Image shows neurons in the cerebral cortex.
Projection neurons of the cerebral cortex targeted for reprogramming are displayed in green (photo 1). It is this reprogramming that is the focus of findings by Harvard researchers including Professor Paola Arlotta (right, photo 2). Among others, Arlotta worked with grad students Mohammed A. Mostajo-Radji (left) and Zhanlei Ye, who were both first authors on the study. Credit: Caroline Rouaux/Arlotta Lab.
A parallel approach may involve reprograming the identity of neurons that are already present in the brain, turning them into and thereby replacing neurons that die in disease. For both strategies, the present study suggests that if the new neurons are of the right type, they may be able to direct the building of proper networks with the endogenous cells.
One of the major focuses today in regenerative neurobiology is to use stem cells to produce and replace neurons killed off by disease, and then implant them into patients’ brains. “What we’re talking about is a parallel approach,” Arlotta said. “Instead of making neurons in a dish from stem cells, an alternative would be to reprogram the identity of other neurons that are resistant to disease and turn them directly into the neurons that die in the brain.
“These are early but exciting days,” Arlotta said. “The work thus far has been done in the brains of young mice, which are far more plastic than adult brains,” she pointed out. The next frontier, she said, is to attempt to reprogram neurons and circuits in older brains.
“If we could do it in an adult brain, it would be immensely powerful.”
About this neuroscience and aging research
Funding: The study was funded by the NIH/National Institute on Aging, and Abbott Nutrition.
Source: B. D. Colen – Harvard
Image Credit: The image is credited to Caroline Rouaux/Arlotta Lab
Original Research: Abstract for “Instructing Perisomatic Inhibition by Direct Lineage Reprogramming of Neocortical Projection Neurons” by Zhanlei Ye, Mohammed A. Mostajo-Radji, Juliana R. Brown, Caroline Rouaux, Giulio Srubek Tomassy, Takao K. Hensch, and Paola Arlotta in Neuron. Published online November 4 2015 doi:10.1016/j.neuron.2015.10.006

3 comments:

  1. Stuff like this gives me some hope that chronic stroke hemi-paresis recovery could be improved, but medical progress is so slow I doubt if I will live long enough!
    I just turned 60 and odds are I will live to age 85!
    I need improvement NOW!

    ReplyDelete
    Replies
    1. I am 59 and I doubt I will ever see any useful chronic stroke rehabilitation in my life because no one has a plan on stroke

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    2. I am 59 and I doubt I will ever see any useful chronic stroke rehabilitation in my life because no one has a plan on stroke

      Delete