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.

Saturday, October 8, 2011

Can magnetism help us control the brain, remotely?

I like the comment about controlling a worm. And I personally think we should attach tPA to them and direct it directly to the clot. It would take a lot smaller amount and probably extend the timeframe a lot without the risk of bleeding.
http://www.physorg.com/news/2011-10-magnetism-brain-remotely.html

Scientists at the University at Buffalo have received $1.3 million from the National Institute of Mental Health (NIMH) to test how tiny, can be used to remotely control neurons in the brains of mice.

If the work is successful, the research team will have given neuroscientists a powerful, new tool: a non-invasive technique for triggering activity deep inside the .

This kind of remote, neuro-stimulation would help researchers learn more about how the brain's complicated controls behavior, leading eventually to better understanding and possibly treatment of ailments that involve the injury or malfunction of specific sets of neurons. Traumatic brain injuries, Parkinson's disease, and peripheral paralysis all fall into this category.

"Our early understanding about the brain's functional regions came from patients who showed changes in their behavior after losing a part of their brain to or a tumor," said Arnd Pralle, the assistant professor of physics who is leading the new UB study. "The ability to now reversibly turn individual cells off or on and to observe the animal's behavior brings us finally to the level of the actual neurological circuit, which is extremely exciting."

The new NIMH funding, which comes from the National Institute of Health's program for Exceptional, Unconventional Research Enabling Knowledge Acceleration (EUREKA), is a testament to the promise of Pralle's work.

He and his colleagues have already succeeded in using their remote control technique to open calcium ion channels, activate neurons in cell culture, and even manipulate the behavior of C. elegans, a tiny worm.

The approach involves the use of heated, in conjunction with some clever genetic engineering.

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Here's how it works in the brain: First, scientists employ harmless viruses to carry a special strand of DNA into the brain. The new genetic material induces specific, targeted cells to build a special ion channel containing a receptor that magnetic nanoparticles will recognize.

When the nanoparticles latch onto these ion channels, scientists apply an alternating magnetic field to the brain that causes the particles' magnetization to flip rapidly, generating heat. That heat then stimulates the ion channels to open, depolarizing the neurons and causing them to fire.

With the new NIMH funding, Pralle's research team plans to test this method on neurons in the olfactory bulb, which lies in the forward region of the brain and controls how animals perceive odors.

Specifically, the scientists will see if they can use the nanoparticles' localized heating to activate specific neurons in the olfactory bulb, causing the mice to "smell" a particular odor even when no actual chemicals are present.

As neuroscientists search for better ways to probe the brain, Pralle's method is particularly attractive because magnetic fields are able to penetrate tissues without harming them. Other methods for remotely controlling brain cells are more invasive, including a state-of-the-art technique involving the use of an implanted optical fiber to stimulate light-activated .

Pralle's prior work on magnetic nanoparticles was supported by the UB 2020 Interdisciplinary Research Development Fund, which provides start-up money to projects with the potential to receive larger, external grants.

That seed funding enabled Pralle and his collaborators to complete a number of studies, including one in which they attached magnetic nanoparticles to cells near the mouth of C. elegans.

When the scientists used their remote technique to heat the nanoparticles, most of the worms began reflexively crawling backward in an attempt to escape the heat when the temperature hit 34 degrees Celsius.

The university is in full compliance with mandates of state and federal regulatory agencies pertaining to the humane use and care of research animals

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