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.

Monday, January 28, 2019

Humans produce new brain cells throughout their lives, say researchers

Well make up your minds and create a protocol so we know EXACTLY how to create them AND MIGRATE them to where they are needed. 

Humans produce new brain cells throughout their lives, say researchers


Humans continue to produce new neurons in a part of their brain involved in learning, memory and emotion throughout adulthood, scientists have revealed, countering previous theories that production stopped after adolescence. The findings could help in developing treatments for neurological conditions such as dementia.
Many new neurons are produced in the hippocampus in babies, but it has been a matter of hot debate whether this continues into adulthood – and if so, whether this rate drops with age as seen in mice and nonhuman primates.
Although some research had found new neurons in the hippocampus of older humans, a recent study scotched the idea, claiming that new neurons in the hippocampus were at undetectable levels by our late teens.
Now another group of scientists have published research that pushes back, revealing the new neurons are produced in this brain region in human adults and does not drop off with age. The findings, they say, could help in the hunt for ways to treat conditions ranging from Alzheimer’s to psychiatric problems.
“The exciting part is that the neurons are there throughout a lifetime,” said Dr Maura Boldrini from Columbia University in New York and first author of the new study published in the journal Cell Stem Cell. “It seems that indeed humans are different from mice – where [neuron production] goes down with age really fast – and this could mean that we need these neurons for our complex learning abilities and cognitive behavioural responses to emotions,” she said.
Boldrini and colleagues looked at the hippocampus in 28 men and women aged between 14 and 79, collected just hours after they had died. Importantly, Boldrini notes, all of the individuals were healthy before death, unlike in many previous studies.
Using a number of techniques, the team examined the degree of new blood vessel formation, the volume, and the number of cells of different stages of maturity, in an area known as the dentate gyrus – the region of the hippocampus where new neurons are produced.
“According to mice studies there are these pluripotent stem cells that are a pool of cells that don’t normally do anything, they are quiescent, and then they can undergo division,” said Boldrini, adding that some studies have suggested that we might be born with a finite pool of these ‘mother cells’. “Those daughter cells are the ones that exponentially divide and make many more cells and differentiate towards becoming a neuron.”
The team found levels of these “mother cells” dropped with age in the front and middle region of the dentate gyrus. However, levels of the cells they give rise to did not drop, with the team finding thousands of new, immature neurons in the dentate gyrus at the time of death regardless of age.
“We can still make enough neurons even with fewer left of these ‘mothers’.” said Boldrini.
However, there was a drop in the front of the dentate gyrus in the number of cells producing substances linked to neuroplasticity – the ability for the brain to change or “rewire”.
“Even though we make these new neurons, they might be less plastic, or maybe making fewer connections or migrating less,” said Boldrini.
The authors note that a drop in plasticity might help explain why even healthy people can become more emotionally vulnerable as they age, but that the formation of new cells including neurons might help protect against cognitive or emotional decline.
Boldrini said it was now important to look at what happens in the brains of those with Alzheimer’s and emotional problems, since if there are differences in the formation of new cells in the hippocampus it could offer scientists new targets for treatment.
Dr Mercedes Paredes from the University of California San Francisco, an author of last month’s paper suggesting adults do not develop new neurons, said she was not persuaded. “For now, we do not think this new study challenges what we have concluded from our own recently published observations: if neurogenesis continues in the adult human hippocampus, it is an extremely rare phenomenon,” she said. “It boils down to interpretation of equivocal cells which we took extra steps to characterise extensively and showed not to be new neurons as they first appeared.”
But Dr Niels Haan from Cardiff University said he was convinced new neurons form in the adult human brain, although their function was as yet unclear.
“We know from work in animal models that adult born neurons are required for various learning and memory processes, and there is some evidence suggesting neurogenesis is disrupted in human psychiatric conditions,” he said. “This is a promising area for potential treatments.”

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