SASKATOON – There’s a stroke every 10 minutes in Canada. Of those, about 10-15 per cent are triggered by arterial ruptures and uncontrolled bleeding in the brain, and are incredibly devastating. These are the strokes that University of Saskatchewan researcher Dr. Mark Hackett studies, with hopes to help improve post-stroke health. 

“Many people initially survive a stroke, but unfortunately a large percentage of the survivors retain long term damage” says Hackett.

Known as intracerebral haemorrhages, these strokes are a major health concern for Canadian men and woman of all ages. Brain damage is immediate and can continue in the hours, days and even weeks following a stroke. That damage can severely affect motor, logic, and verbal skills, and without immediate treatment, the brain can lose as many brain cells every hour as it does in about three and a half years of normal aging.

It is impossible to treat stroke immediately, even if you have a stroke in-hospital. That means that the best way to protect stroke victims is to understand the mechanisms behind damage after a stroke, and basic research is vital to developing therapies to reduce brain injury and improving stroke victims’ quality of life, which is exactly the sort of data Hackett’s team collects.

“We hope that by identifying mechanisms or harmful processes that are activated during intracerebral haemorrhage which then drive brain damage, we may be able to develop new therapeutic options for stroke patients. Such new therapies may help minimise or in some case prevent the loss of motor, logic, and verbal skills that occur after stroke” says Hackett.            

In order to identify the pathways responsible for delayed brain cell damage, the team needed to precisely visualize chemicals in the brain.

Visualizations of brain tissues help indicate the toxic iron pathways following haemorrhagic stroke. This data is vital to developing effective treatments for this severe type of stroke.

Iron released into the brain from blood is thought to be a major contributing factor in chemical reactions that damage brain tissue after a haemorrhagic stroke. However, the brain has its own defense mechanisms that act to detoxify the iron released from blood, and being able to identify toxic and detoxified iron is key to developing effective stroke therapies.

“There are other techniques that you could use to detect harmful iron in the brain, but it would require dissecting a piece of tissue and grinding it up. Then information about exactly which brain cells have harmful iron is lost,” says Hackett. So, Hackett developed a new synchrotron method to identify dangerous forms of iron in the brain.

Specifically, their new imaging method combines Raman spectroscopy, a technique commonly used for chemical analysis, and synchrotron-based X-ray Fluorescence Imaging, which can visualize the distribution of iron down to the cellular and even subcellular levels. Using this combination of techniques, it was possible for the team to not only identify where iron was present in the brain, but where and when it was dangerous to the brain’s health.

The SMI team has now started new studies where they are using this suite of imaging tools to study how several potential therapeutic strategies may alter the amounts and location of toxic and non-toxic iron within the brain after intracerebral haemorrhage. They hope that this knowledge will then translate to the clinical setting for improved therapies for stroke victims.

This work was performed by members of the Synchrotron Medical Imaging Team, an international collaboration of researchers who use advanced synchrotron techniques to better understand stroke. The team receives funding from the Canadian Institutes of Health Research and the Heart and Stroke Foundation of Canada.
Fred Colbourne is a Canada Research Chair in Intracerebral Hemorrhagic Stroke.
Mark Hackett has been supported by a Saskatchewan Health Research Foundation fellowship, a Canadian Institute of Health Research fellowship and is a CIHR-THRUST fellow.

Cite: Hackett, M. J., Desouza, M., Caine, S., Bewer, B., Nichol, H., Paterson, P. G., & Colbourne, F. (2015). A new method to image heme-Fe, total Fe and aggregated protein levels after intra-cerebral hemorrhage. ACS chemical neuroscience. DOI: 10.1021/acschemneuro.5b00037

About the CLS:

The Canadian Light Source is Canada’s national centre for synchrotron research and a global centre of excellence in synchrotron science and its applications. Located on the University of Saskatchewan campus in Saskatoon, the CLS has hosted over 2,000 researchers from academic institutions, government, and industry from 10 provinces and 2 territories; delivered over 32,000 experimental shifts; received over 8,300 user visits; and provided a scientific service critical in over 1,000 scientific publications, since beginning operations in 2005. The CLS has over 200 full-time employees.

CLS operations are funded by Canada Foundation for Innovation, Natural Sciences and Engineering Research Council, Western Economic Diversification Canada, National Research Council of Canada, Canadian Institutes of Health Research, the Government of Saskatchewan and the University of Saskatchewan.

Synchrotrons work by accelerating electrons in a tube to nearly the speed of light using powerful magnets and radio frequency waves. By manipulating the electrons, scientists can select different forms of very bright light using a spectrum of X-ray, infrared, and ultraviolet light to conduct experiments.

Synchrotrons are used to probe the structure of matter and analyze a host of physical, chemical, geological and biological processes. Information obtained by scientists can be used to help design new drugs, examine the structure of surfaces in order to develop more effective motor oils, build more powerful computer chips, develop new materials for safer medical implants, and help clean up mining wastes, to name a few applications.

For more information visit the CLS website or contact:

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1 (306) 657-3771 

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