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, October 10, 2017

Injectable Functionalized Self-assembling Nanopeptide Hydrogel on Angiogenesis and Neurogenesis for Central Nervous System Regeneration

Ok, WHOM is going to follow this up in humans? Zebrafish are ok but we need to get to primates. 
http://pubs.rsc.org/en/content/articlelanding/2017/nr/c7nr06528k#!divAbstract
Could we do nasal route instead of injections?

Abstract

Brain injury is a devastating medical condition and represents a major health problem. For such disease, tissue and organ reconstruction has been regarded as a promising therapeutic strategy. Here, we propose a regenerative methodology focusing on the provision of functionalized nanopeptide scaffold to facilitate angiogenesis and neurogenesis at the brain injury site. The peptide, RADA16-SVVYGLR, undergoes self-assembling process to construct an interconnected network with intertwining nanofibers and can be controlled to display various physicochemical properties by the adjustment of microenvironmental factors such as pH value and ions concentration. Such scaffold is capable of supporting endothelial cells to form tube-like structure and neural stem cells to survive and proliferate. In in vivo zebrafish brain injury model, sprouting angiogenesis and developmental neurogenesis are achieved, and functional recovery of severed optic tectum is effectively enhanced in RADA16-SVVYGLR hydrogel-implanted group. Meanwhile, the nanopeptide hydrogel is non-toxic to zebrafish embryo during embryonic developmental stage. The angiogenic self-assembling peptide hydrogel has programmable physical properties, good biocompatibility, and regenerative ability for functional recovery in the injured brain. We suggest that functionalized self-assembling peptide encapsulated with neural stem cells or used alone could be an attractive and effective therapeutic modality for the applications in brain injury and diseases (viz., trauma, stroke, tumor, degenerative neurological disorder, etc).

No comments:

Post a Comment