Are you lucky enough to have killed off your inactive cells? what does your doctor think?
http://www.alphagalileo.org/ViewItem.aspx?ItemId=169983&CultureCode=en
For the first time, Tübingen neuroscientists were able to
differentiate between active and inactive cells in the brain
morphologically, i.e. based on the cells’ structure. Investigating
granule cells in the rat’s brain, they found a much larger proportion of
inactive than active cells.
Many things we think we know about the world have their origin in
popular culture, not science. The most well-known false ‘fact’ about the
brain is the misconception that we only use ten percent of the brain’s
overall capacity. This so-called ’ten percent myth’, while accepted as
such by neuroscientists, still regularly figures in advertisement, but
also in books and short stories as well as films. As with any myth,
however, there is a kernel of truth at the core of the matter: many
neurons remain dormant for most if not all of our life, even while their
direct neighbours show regular activity.
A team of neuroscientists led by Dr. Andrea Burgalossi of the Werner
Reichardt Centre for Integrative Neuroscience (CIN) at the University of
Tübingen have now taken an important step towards understanding why
some neurons are active and others are not: they can tell them apart
morphologically. To be able to do so, the investigators employed
so-called juxtacellular recordings in freely-moving rats. With this
technique, electrodes are inserted right next to individual, functioning
neurons in live organisms. This allows recording action potentials from
these neurons while they work, and while simultaneously identifying the
cells that the recordings are taken from for later analysis.
During this analysis, morphological traits of the analysed cells are
identified, most importantly their dendritic arbors, i.e. the filament
structures which receive input signals from other neurons. The cells
under investigation were granule cells (GCs) in the rat’s dentate gyrus
(DG). Dentate GCs have been shown to be intimately connected to
individual memories of places and individuals, and thus playing a
central role in memory tasks.
The researchers recorded from 190 GCs, only 27 of which they found to
be active (ca. 14 percent). While this seems to give credibility to the
‘ten percent myth’, the team actually expected this outcome, as the DG
is a brain structure where in any given task, only a very small
percentage of neurons take part, while their neighbours remain dormant,
waiting for their ‘cue’, as it were. Memory functions in the brain work
according to a principle that neuroscientists call ‘sparse coding’, i.e.
a comparatively small number of neurons encode complex information –
possibly to make overlap between different memories more unlikely.
Using a smaller subsample, the scientists looked for correlations
between active and passive functionality and the respective cells’
morphology. Their results show that active GCs have much more complex
dendritic arbors. They not only transfer and receive information from
many more neurons than the inactive ones, they also have better cellular
‘infrastructure’ to do so. Despite their as of yet limited sampling,
the scientists are positive that they can now tell apart active and
inactive GCs, mostly by merely looking at them. “Explaining the causes
of activity in some and inactivity in other neurons may still take a
long time”, cautions Burgalossi, leader of the research group. “But
finding a direct link between function and morphology is an important
step forward. It will be even more challenging to find evidence of
causality. But we are on the right track.”
Use the labels in the right column to find what you want. Or you can go thru them one by one, there are only 29,302 posts. Searching is done in the search box in upper left corner. I blog on anything to do with stroke. DO NOT DO ANYTHING SUGGESTED HERE AS I AM NOT MEDICALLY TRAINED, YOUR DOCTOR IS, LISTEN TO THEM. BUT I BET THEY DON'T KNOW HOW TO GET YOU 100% RECOVERED. I DON'T EITHER BUT HAVE PLENTY OF QUESTIONS FOR YOUR DOCTOR TO ANSWER.
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, November 16, 2016
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