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.

Wednesday, July 7, 2021

'Zombie cells' hold clues to spinal cord injury repair

 Will this do the same for stroke? WHOM do we ask to do the followup research? Specific names only. With NO LEADERSHIP AND NO STRATEGY NOTHING WILL BE DONE.

 

'Zombie cells' hold clues to spinal cord injury repair

The image represents a transversal cross-section of a mouse spinal cord. Neuronal cell bodies are represented in light blue delineating the butterfly shape characteristic of the gray matter, while glial projections are represented in orange-red. Credit: Diogo Paramos-de-Carvalho

Mammals have a poor ability to recover after a spinal cord injury, which can result in paralysis. A main reason for this is the formation of a complex scar associated with chronic inflammation that produces a cellular microenvironment blocking tissue repair. Now, a research team led by Leonor Saude, group leader at Instituto de Medicina Molecular Joao Lobo Antunes (iMM; Portugal) and Professor at Faculdade de Medicina da Universidade de Lisboa, have shown that the administration of drugs that target specific cellular components of this scar improve functional recovery after injury. The results now published in the scientific journal Cell Reports set the basis for a new promising therapeutic strategy not only for spinal cord injuries, but potentially for other organs that lack regenerative competence.

This study was performed at iMM with collaboration from researchers at CEDOC NOVA Medical School and was funded by "la Caixa" Foundation—CaixaResearch Call and Fundacao para a Ciencia e a Tecnologia (Portugal).

Leonor Saude and her team have been studying spinal cord using two different models: zebrafish, which exhibit spinal injury recovery, and mammals, which show poor recovery. The dense scar that forms at the lesion site has been of particular interest. In mammals, upon spinal cord injury, researchers observed that cells start to accumulate at the lesion periphery. But not any cells: "These cells are known as senescent cells. They have specific features and markers and are what we can call 'zombie cells', where growth and division is interrupted, but where the normal cell death program is not activated," explains Leonor Saude.

"While in zebrafish, the accumulation of these cells at the injury periphery is cleared out over time, in mammals, these cells persist and are important components of the dense scar observed. Because senescent cells have specific molecular markers, there are specific drugs that could be tested in this context," says Diogo Paramos-de-Carvalho, first author of the study. "With the administration of different senolytic drugs, that specifically target these , we have observed a progressive decrease of these , a decrease in the scar extension and lower levels of inflammation due to a decreased secretion of pro-fibrotic and pro-inflammatory factors. The observed changes at the underlie the improved locomotor, sensory and bladder functions that we have also found," explains Isaura Martins, also first author of the study.

"Although we are still far from healing spinal cord injuries in humans, we are learning more about the molecular signatures of these lesions and these new promising results can open new therapeutic strategies that can be applied not only to but in other conditions that lack regenerative competence," says Leonor Saude.

 

No comments:

Post a Comment