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, November 17, 2017

New dye gives scientists a clearer insight into the brain

We should be able to use this to listen in on the signals being passed as neuroplasticity occurs. Then we might be able to make neuroplasticity repeatable.
And matching it with this could make understanding neuronal signals easy. Now we just need our stroke medical 'professionals' to put two and two together and we might make progress in 50 years. Long after I'm dead.

Hi-Res Probes Will Change Our Understanding of the Brain

New dye gives scientists a clearer insight into the brain

14 November 2017 Keele University
Keele University researchers have designed a new dye that can be used to observe the electrical activity of neurons in the brain and could lead to finding a new and more efficient way of treating neurological diseases, as presented at the prestigious Society for Neuroscience annual conference in Washington, D.C. this week.
As part of a two-year collaborative study between neuroscientists at Keele University and chemists at Newcastle University, funded by the Leverhulme Trust, a new near-infrared voltage-sensitive dye has been designed - JULBD6 - which offers comparable signal quality and toxicity when compared to the commonly used voltage-sensitive dye di-4-ANEPPS. These findings were recently published in Chemistry: A European Journal.
To observe networks of neurons and their interactions, neuroscientists most commonly use calcium imaging or voltage-sensitive dyes. Voltage-sensitive dyes respond to neuronal events faster than calcium dyes, allowing single neuron spikes to be observed as a change in fluorescence, but a major limitation of voltage-sensitive dyes is that the observed fluorescent changes are weaker than calcium dyes, which this research project aimed to improve.
A clearer insight into neuronal networks could improve treatment for neurological diseases, for example it may help further uncover how neuromodulators, such as dopamine, impact the functionality of neural circuits, which could lead to finding a new and more efficient way of treating people with Parkinson’s disease.
Keele University Research Associate Dr John Butcher commented: “This could have a large impact on neuroscience as a field. The structure of the new dye, JULBD6, is completely different from other dyes such as the widely used di-4-ANEPPS, but offers the same signal quality in terms of the change in fluorescence during neuronal spiking and does not affect the health of the neurons.”
Professor Peter Andras, the Keele lead on the project, said: “These results are very promising as we have shown a completely new voltage-sensitive dye that allows rational design of key molecular features and offers similar performance to other dyes which are widely used in neuroscience. This dye is also in the near-infrared range, rather than some green dyes which have higher toxicity, making it more suited to longitudinal studies. Based on these findings we now aim to design dyes based on the structure of JULBD6 in order to improve the fluorescence signal quality whilst making them as less toxic as possible. This new technology could really benefit neuron imaging studies.”

Attached files

  • fluorescent brain scan

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