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.

Tuesday, December 17, 2024

Lab-Grown Neurons Mimic Brain Networks, Exhibit Neuroplasticity

 The simple next goal is to listen in on neurons signaling each other to drop your current function and take on your neighbors' functions. You can easily do that by these methods.  Until that is figured out neuroplasticity will never be repeatable on demand.  

1. Use nanowires to listen in on single neurons

2. Or lay a grid across the cortex to listen in. 

Lab-Grown Neurons Mimic Brain Networks, Exhibit Neuroplasticity

Summary: Researchers have developed lab-grown neurons that behave more like real brain networks, advancing the study of learning and memory. Using microfluidic devices, the neurons formed diverse and functional networks, resembling those seen in living nervous systems.

These networks exhibited complex activity patterns and showed neural plasticity, reconfiguring in response to repetitive stimulation. This breakthrough provides scientists with a powerful new tool to study brain functions under controlled lab conditions.

Key Facts

  • Realistic Networks: Microfluidic devices enabled neurons to form natural-like brain networks.
  • Neural Plasticity: Repeated stimulation altered neuronal ensembles, mimicking learning processes.
  • Advanced Models: This technology can be used to study memory formation and brain function.

Source: Tohoku University

“Neurons that fire together, wire together” describes the neural plasticity seen in human brains, but neurons grown in a dish don’t seem to follow these rules. Neurons that are cultured in-vitro form random and meaningless networks that all fire together. They don’t accurately represent how a real brain would learn, so we can only draw limited conclusions from studying it.

But what if we could develop in-vitro neurons that actually behaved more naturally?

A research team at Tohoku University has used microfluidic devices to reconstitute biological neuronal networks bearing connectivity resembling that found in animal nervous systems.

This shows a neuron.
By changing the size and shape of the tiny tunnels (called microchannels) that connect the neurons, the team controlled how strongly the neurons interacted. Credit: Neuroscience News

They showed that such networks exhibit complex activity patterns that were able to be “reconfigured” by repetitive stimulation. This remarkable finding provides new tools for studying learning and memory.

The results were published online in Advanced Materials Technologies on November 23, 2024.

In certain areas of the brain, information is encoded and stored as “neuronal ensembles,” or groups of neurons that fire together. Ensembles change based on input signals from the environment, which is considered to be the neural basis of how we learn and remember things. However, studying these processes using animal models is difficult because of its complex structure.

“The reason there is a need to grow neurons in the lab is because the systems are much simpler,” remarks Hideaki Yamamoto (Tohoku University), “Lab-grown neurons allow scientists to explore how learning and memory work in highly controlled conditions. There is a demand for these neurons to be as close to the real thing as possible.”

The research team created a special model using a microfluidic device–a small chip with tiny 3D structures. This device allowed neurons to connect and form networks similar to those in the animals’ nervous system. By changing the size and shape of the tiny tunnels (called microchannels) that connect the neurons, the team controlled how strongly the neurons interacted.

The researchers demonstrated that networks with smaller microchannels can maintain diverse neuronal ensembles. For example, the in-vitro neurons grown in traditional devices tended to only exhibit a single ensemble, while those grown with the smaller microchannels showed up to six ensembles.

Additionally, the team found that repeated stimulation modulates these ensembles, showing a process resembling neural plasticity, as if the cells were being reconfigured.

This microfluid technology in conjunction with in-vitro neurons could be used in the future to develop more advanced models that can mimic specific brain functions, like forming and recalling memories.

About this neuroplasticity research news

Author: Public Relations
Source: Tohoku University
Contact: Public Relations – Tohoku University
Image: The image is credited to Neuroscience News

Original Research: Open access.
Precision Microfluidic Control of Neuronal Ensembles in Cultured Cortical Networks” by Hideaki Yamamoto et al. Advanced Materials Technologies

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