Interesting stuff to followup on which will never occur.
http://www.news-medical.net/news/20170203/Study-provides-insights-into-functions-of-astrocytes-following-brain-injury-or-disease.aspx
Astrocytes have long been implicated in the pathology of a range of
human neurodegenerative diseases or injuries including Alzheimer's,
Huntington's Parkinson's disease, brain trauma and spinal cord injury.
But how they are produced and what their roles in disease may be, has
been as yet unknown. This paper provides an understanding of the
mechanism involved and for the first time provides hope that a lot of
these diseases may in fact be treatable.
The study, published recently in Nature and led by
researchers at The University of Melbourne and Stanford University,
provides deeper understanding of the functions of injured or diseased
astrocytes found in the Central Nervous System (CNS) following acute
injury and chronic neurodegenerative disease.
In a healthy brain, astrocytes are vital for the normal functioning
of the brain - providing nutrients to support neuron viability,
releasing factors that aid formation of connections between nerve cells
known as synapses, as well as many other important functions.
One
puzzle has been that in some circumstances the astrocytes appear to
have a toxic effect on neurons, whereas in others they support neuronal
viability and connectivity.
Researcher Dr Shane Liddelow from the University of Melbourne's
Department of Pharmacology and Therapeutics, and the Department of
Neurobiology at Stanford University, said astrocytes are often
characterised as 'helper' cells but they can also contribute to damage
caused by brain injury and disease by turning toxic and kill other types
of brain cells.
"These apparently opposing effects have been a puzzle for some time.
By characterising two types of astrocytes this paper provides some
answers to the puzzle," he said.
"Following nerve damage, astrocytes form scar tissue that can help in
the regeneration of severed fibres. But we have also discovered that
under certain conditions, they can turn and become negatively reactive,
causing cell death," Dr Liddelow said
For many decades, the trauma and neurodegeneration research focus has
been on neurons. Researchers are excited by the discovery of these
neurotoxic reactive astrocytes, because for the first time, these
findings imply that acute injuries of the retina, brain and spinal cord
and chronic neurodegenerative diseases, may all be much more treatable
and even reversible than first thought.
By providing new insights into the process of neurodegeneration,
researchers can look at new pathways for dealing with neurological
diseases and injuries, by targetting these toxic astrocytes, in addition
to neurones in neuropsychiatric diseases or oligodendrocytes as for
instance in multiple sclerosis.
Ultimately, there is still hope that one day it may be possible to
switch back astrocytes from the "toxic" to the "helper" state, a long
term target for Dr. Liddelow and colleagues.
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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.
Saturday, February 11, 2017
Study provides insights into functions of astrocytes following brain injury or disease
Labels:
astrocytes,
followup,
never occur
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