Eccles Institute of Neuroscience Seminar Series: Cerebral ischaemia: Novel mechanisms and potential therapies

Associate Professor Chris Sobey,  NHMRC Senior Research Fellow & Department of Pharmacology, Monash University.

Strokes are a major killer, second only to heart disease, but they are also a leading cause of adult disability. Many survivors are left severely incapacitated. Because strokes mainly affect older people, they will be an increasing problem for an ageing population. But little can be done to limit their damage.

Most strokes are caused by a blockage of blood to the brain: neurons die very quickly without oxygen. A ‘clot-buster’ drug called tPA can help restore blood flow, but has limited use as it must be given within several hours and will help only some types of stroke.  

Chris, an NHMRC senior research fellow whose work is also supported by the National Heart Foundation, is interested in cardiovascular research generally. As a pharmacologist he is in the business of identifying new treatments, and has an interest in both drug and cell-based therapies. 

His group’s drug research is based on awareness that the initial damage caused by a stroke tends to worsen during the following hours or days. 

This is probably related to inflammation sparked by white blood cells rushing into the brain. Their role is to repair, but they may create more problems as they cause the tissue to swell. The brain, in its hard skull, cannot expand as injured tissue elsewhere can, so pressure builds up, preventing more blood coming in.

“There’s a real case for drugs to be developed to be given in conjunction with the tPA, to quieten the inflammation down,” Chris says. 

“There’s lots of sophisticated signalling that underlies the entrance of these white blood cells to the brain. We’re trying to understand which ones we should be trying to block and which ones we should be trying to enhance and what drugs are the best to do that.”

While this work is sufficiently advanced to give hope, it is Chris’s work on stem cells that really fires the imagination. He uses cells from the amniotic fluid that surrounds a baby in the womb, and is usually discarded at birth. 

These cells have extraordinary healing capacity, he says, going to wherever damage has occurred and repairing it. Unlike a drug, which needs repeated doses, they continue working for a period of time: “I think of them as little pharmacies coming in to where they need to be.” 

Given soon after a stroke, the cells reduce damage. Perhaps even more remarkably, it seems that even if they are administered days later, they can help promote the capacity of the undamaged part of the brain to pick up lost functions.

Date & time

3.30–4.30pm 25 May 2012


The Finkel Lecture Theatre, The John Curtin School of Medical Research, Building 131, Garran Road, ANU


 Danielle Khalidi
 +61 2 612 53926

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