Use the labels in the right column to find what you want. Or you can go thru them one by one, there are only 29,42 posts. Searching is done in the search box in upper left corner. I blog on anything to do with stroke. DO NOT DO ANYTHING SUGGESTED HERE AS I AM NOT MEDICALLY TRAINED, YOUR DOCTOR IS, LISTEN TO THEM. BUT I BET THEY DON'T KNOW HOW TO GET YOU 100% RECOVERED. I DON'T EITHER BUT HAVE PLENTY OF QUESTIONS FOR YOUR DOCTOR TO ANSWER.
Saturday, October 10, 2015
Three-dimensional macroporous nanoelectronic networks as minimally invasive brain probes
This seems like it would be very useful for our stroke researchers to listen in on neurons talking to each other. Then we could maybe find out exactly how neuroplasticity works. Why would a neuron give up its' current task to help out a neighboring neuron? How is that accomplished? Without knowing these answers neuroplasticity is not consistently repeatable. Which means that none of the research into neuroplasticity is valid right now.
The other possibilities for listening in on the brain:
Direct electrical recording and stimulation of neural
activity using micro-fabricated silicon and metal micro-wire probes have
contributed extensively to basic neuroscience and therapeutic
applications; however, the dimensional and mechanical mismatch of these
probes with the brain tissue limits their stability in chronic implants
and decreases the neuron–device contact. Here, we demonstrate the
realization of a three-dimensional macroporous nanoelectronic brain
probe that combines ultra-flexibility and subcellular feature sizes to
overcome these limitations. Built-in strains controlling the local
geometry of the macroporous devices are designed to optimize the
neuron/probe interface and to promote integration with the brain tissue
while introducing minimal mechanical perturbation. The ultra-flexible
probes were implanted frozen into rodent brains and used to record
multiplexed local field potentials and single-unit action potentials
from the somatosensory cortex. Significantly, histology analysis
revealed filling-in of neural tissue through the macroporous network and
attractive neuron–probe interactions, consistent with long-term
biocompatibility of the device.
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