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, January 6, 2017

Of mice and men: Unique electrical properties of human nerve cells make a difference

So does this explain  rodent inflammation is not the same as human inflammation? And the reason that  Dr. Michael.Tymianski@uhn.ca has stated that 1000+ neuroprotective trials have failed? It is a damned simple question that will never be answered because we don't have smart enough people in the stroke medical world. Oops, not following Dale Carnegie again.
http://www.alphagalileo.org/ViewItem.aspx?ItemId=171346&CultureCode=en
The human brain’s advanced cognitive capabilities are often attributed to our recently evolved neocortex. Comparison of human and rodent brains shows that the human cortex is thicker, contains more white matter, has larger neurons, and its abundant pyramidal cells (formerly called “psychic” neurons) have more synaptic connections per cell as compared to rodents.
However, scientists have yet to determine whether there are important differences at the biophysical level of the basic building blocks of the human neocortex, the pyramidal neurons. Do these cells possess unique biophysical properties that might impact on cortical computations?
To answer this question, a theoretical team led by Prof. Idan Segev from the Hebrew University of Jerusalem, working with experimental colleagues at Vrije Universiteit Amsterdam and Instituto Cajal in Madrid, built detailed 3D models of pyramidal cells from the human temporal neocortex. These first-ever detailed models of human neurons were based on in vitro intracellular physiological and anatomical data from human cells.
(To collect this data, fresh cortical tissue was obtained from brain operations at a neurosurgical department in Amsterdam, and additional data was obtained from light-microscope studies in pyramidal cells from post mortem studies at the Cajal Institute in Madrid.)
The theoretical study predicted that layer 2/3 pyramidal neurons from the human temporal cortex would have a specific membrane capacitance that is half of the commonly accepted “universal” value for biological membranes (~0.5 µF/cm2 vs. ~1 µF/cm2). Since membrane capacitance affects how quickly a cell can respond to its synaptic inputs, this finding has important implications for the transmission of signals within and between cells. The theoretical prediction regarding the specific membrane capacitance was then validated experimentally by direct measurements of membrane capacitance in human pyramidal neurons.
“This is the first direct evidence for the unique electrical properties of human neurons,” said researcher Guy Eyal, a Ph.D. student at the Hebrew University’s Department of Neurobiology. “Our finding shows that low membrane capacitance significantly improves the efficacy of signal processing and the speed of communication within and between cortical neurons in the human neocortex, as compared to rodents.”
“The results of this work imply that human cortical neurons are efficient electrical microchips, compensating for the larger brain and large cells in humans, and processing sensory information more effectively,” said Prof. Idan Segev from the Department of Neurobiology and the Edmond and Lily Safra Center for Brain Sciences at the Hebrew University. “Indeed, the study shows that already at the level of the individual building blocks of the nervous system (the nerve cells), humans are distinct as compared to rodents. More research should be performed in this direction on non-human primates.”
The researchers suggest the distinctive biophysical membrane properties of human pyramidal neurons are an outcome of evolutionary pressure to compensate for the increase in size and distances in the human brain.

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