Cellular ‘puncture repair kit’ to lessen brain trauma

July 1st, 2008 - 6:47 pm ICT by ANI  

London, July 1 (ANI): Punchstock researchers have developed a ‘puncture repair kit’ for cells, that would repair burst cell membranes in the brain, just like puncture sealants are used in bicycle tyres, and would thus help prevent brain damage after serious head injuries.
This new treatment may also help trauma victims avoid the severest injuries and the researchers showed that when brain-injured rats that are injected with a polymer called polyethylene glycol (PEG) soon after their injuries, they recover certain behavioural abilities better than untreated rats.
According to the author of the study, Richard Borgens of Purdue University in West Lafayette, Indiana said that the therapy “does not require sophisticated technology.
“It requires sophisticated thinking. It acts by absorbing water, promoting the healing of cell membranes and preventing “the exchange of things that cause decay and degeneration of the cell, Nature quoted Borgens, as saying.
He further added that the moment PEG reaches human trials; it could be carried by trauma units and administered as soon as emergency crews reach victims of blunt-force trauma.
In order to get uniform results, the authors gave a standard injury known to damage certain regions of the brain by dropping a weight onto 47 rats. Then the researchers injected a solution of PEG into the rats’ bloodstreams 2 hours, 4 hours or 6 hours after the injury.
It was found that the PEG treatment successfully improved behavioural results for the rats treated within 4 hours of injury. Also, people who were treated after a six-hour delay did not recover any more behavioural performance than the untreated rats.
David Brody of Washington University School of Medicine in St. Louis, Missouri, said that the behavioural test was innovative, as earlier studies with PEG and a related compound called poloxamer-188 have generally measured only their effect on tissues.
“These therapeutics could have side effects that would render the behavioural abnormalities worse, even if the histological abnormalities were improved, so it is very important that behavioural assessments are performed,” said Brody.
However, he warned that it is still too early to know whether humans will show similar results. For example, even though benefits are seen in rats treated up to 4 hours after injury, he said that “we dont know what that will translate to when this moves to human clinical testing”.
While Borgens said that the treatment will go for clinical testing within two years by an industrial licensee, but he claims that this work is gradual and is not a cure for victims of brain injuries.
“The idea that one treatment is going to give them an enormous change in quality of life or actually cure them is foolishness. We shouldnt talk about that. What we should talk about is how we can improve their quality of life, he said.
The study is published in this weeks Journal of Biological Engineering 1. (ANI)

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