Protein could prevent brain damage caused by stroke
The University of Queensland News Mar 30, 2017
A small protein that could protect the brain from stroke–induced injury has been discovered by researchers from The University of Queensland and Monash University.
UQ Institute for Molecular Bioscience researcher Professor Glenn King, who led the research, said the small protein showed great promise as a future stroke treatment.
ÂWe believe that we have, for the first time, found a way to minimise the effects of brain damage after a stroke, Professor King said.
ÂThe small protein we discovered, Hi1a, blocks acid–sensing ion channels in the brain, which are key drivers of brain damage after stroke.
ÂDuring preclinical studies, we found that a single dose of Hi1a administered up to eight hours after stroke protected brain tissue and drastically improved neurological performance.
ÂThis world–first discovery will help us provide better outcomes for stroke survivors by limiting the brain damage and disability caused by this devastating injury.Â
Stroke claims six million lives worldwide each year, and five million survivors are left with a permanent disability.
The Royal Melbourne HospitalÂs Melbourne Brain Centre Director Professor Stephen Davis AM said the preclinical work was very promising.
"A safe and effective neuroprotectant could be given in the ambulance to most stroke patients before hospital arrival and enable many more stroke victims to be treated, Professor Davis said.
ÂThe next step is to determine whether these very encouraging results can be translated into successful human benefits in clinical trials.Â
Professor King said he hoped this discovery could radically improve outcomes for stroke patients.
ÂOne of the most exciting things about Hi1a is that it provides exceptional levels of protection for eight hours after stroke onset, which is a remarkably long window of opportunity for treatment, he said.
ÂHi1a even provides some protection to the core brain region most affected by oxygen deprivation, which is generally considered unrecoverable due to the rapid cell death caused by stroke.
ÂWe are now working to secure financial support to fast–track this promising stroke therapy towards clinical trials.Â
This research was published in Proceedings of the National Academy of Sciences journal.
Go to Original
UQ Institute for Molecular Bioscience researcher Professor Glenn King, who led the research, said the small protein showed great promise as a future stroke treatment.
ÂWe believe that we have, for the first time, found a way to minimise the effects of brain damage after a stroke, Professor King said.
ÂThe small protein we discovered, Hi1a, blocks acid–sensing ion channels in the brain, which are key drivers of brain damage after stroke.
ÂDuring preclinical studies, we found that a single dose of Hi1a administered up to eight hours after stroke protected brain tissue and drastically improved neurological performance.
ÂThis world–first discovery will help us provide better outcomes for stroke survivors by limiting the brain damage and disability caused by this devastating injury.Â
Stroke claims six million lives worldwide each year, and five million survivors are left with a permanent disability.
The Royal Melbourne HospitalÂs Melbourne Brain Centre Director Professor Stephen Davis AM said the preclinical work was very promising.
"A safe and effective neuroprotectant could be given in the ambulance to most stroke patients before hospital arrival and enable many more stroke victims to be treated, Professor Davis said.
ÂThe next step is to determine whether these very encouraging results can be translated into successful human benefits in clinical trials.Â
Professor King said he hoped this discovery could radically improve outcomes for stroke patients.
ÂOne of the most exciting things about Hi1a is that it provides exceptional levels of protection for eight hours after stroke onset, which is a remarkably long window of opportunity for treatment, he said.
ÂHi1a even provides some protection to the core brain region most affected by oxygen deprivation, which is generally considered unrecoverable due to the rapid cell death caused by stroke.
ÂWe are now working to secure financial support to fast–track this promising stroke therapy towards clinical trials.Â
This research was published in Proceedings of the National Academy of Sciences journal.
Only Doctors with an M3 India account can read this article. Sign up for free or login with your existing account.
4 reasons why Doctors love M3 India
-
Exclusive Write-ups & Webinars by KOLs
-
Daily Quiz by specialty
-
Paid Market Research Surveys
-
Case discussions, News & Journals' summaries