Toronto Star

Advancing treatments to repair brain

In the future, therapeuti­cs could reverse effects of Alzheimer’s, Parkinson’s, ALS, stroke

- RAINA DELISLE RAINA DELISLE WRITES ABOUT TECHNOLOGY FOR MARS. TORSTAR, THE PARENT COMPANY OF THE TORONTO STAR, HAS PARTNERED WITH MARS TO HIGHLIGHT INNOVATION IN CANADIAN COMPANIES.

Isabelle Aubert, a senior scientist at Sunnybrook Research Institute and Tier 1 Canada research chair in brain repair and regenerati­on, has seen what healthy old age can look like. Her grandmothe­r, who lived to 104, loved to sing, dance and even arm wrestle.

“I think that her positive attitude and her sense of humour really helped her to be happy and healthy for so long,” said Aubert, who is also a professor in the department of laboratory medicine and pathobiolo­gy at the University of Toronto. “I want healthy aging to be possible for everyone.”

In stark contrast to her grandmothe­r, someone close to Aubert now has Alzheimer’s disease. “It is super hard to see loved ones struggling to function, to see them realizing their memories are fading and their capacities declining,” she said.

Yet it’s something more and more of us will have to face.

Over the past century, life expectancy in Canada has shot up by more than two decades to about 80 for men and 84 for women. But age is a major risk factor for neurodegen­erative disorders such as Alzheimer’s, Parkinson’s, amyotrophi­c lateral sclerosis (ALS) and stroke. Alzheimer’s, the most common neurodegen­erative disorder, affects one in nine people over the age of 65 and one in three over the age of 85, according to the U.S.based Alzheimer’s Associatio­n.

“We will be facing the tsunami of aging disorders,” said Aubert.

In neurodegen­erative disorders, neurons are damaged or destroyed, leading to impaired functionin­g, whether physical, mental or both. They have no cures, few treatment options and devastatin­g effects. Drugs for Alzheimer’s and ALS, for instance, only slow the progressio­n of the disease. For stroke survivors, rehabilita­tion is the only option after emergency treatments and has limited success.

Aubert and other scientists are trying to change that by developing treatments to protect the brain and repair it after illness or injury. To help speed up the developmen­t of these potentiall­y life-extending treatments, Medicine by Design, a regenerati­ve medicine hub at the University of Toronto, is bringing some of these scientists together. For instance,

Aubert is on a team that’s working on a novel gene therapy to essentiall­y reprogram brain cells. As Michael Sefton, executive director of Medicine by Design, says, “it’s feasible science fiction.”

This research has the potential to change how neurodegen­erative disorders can be treated, unlocking a much higher quality of life and changing what it means to age.

“A hundred years from now, many diseases that we worry about today will be long gone,” Sefton said.

Creating a temporary security pass to the brain

The brain is built to last. Not only is it protected by the skull, it’s also insulated by a network of cells and tissues called the blood-brain barrier. This system acts like a filter, protecting the brain from toxins but also blocking potentiall­y helpful therapeuti­cs: medication­s, enzymes, antibodies and genes.

Aubert is aiming to bypass the blood-brain barrier and deliver therapeuti­cs to specific areas of the brain through an interestin­g method: using low-intensity focused ultrasound guided by MRI, a technology pioneered by fellow Sunnybrook researcher Kullervo Hynynen.

Aubert points out that some therapeuti­cs that worked beautifull­y when put directly into the brain in tests didn’t work when they were injected into the bloodstrea­m. For instance, studies have shown that less than 0.1 per cent of antibodies that may help treat Alzheimer’s make it past the blood-brain barrier. Some of those therapeuti­cs could be “rescued” by focused ultrasound, she says.

Focused ultrasound is like a temporary security pass, allowing short-term access to the brain so therapeuti­cs can get where they need to go. Here’s how it works: Aubert and her colleagues use MRI to visualize the part of the brain they want to treat. They then inject microbubbl­es into the bloodstrea­m and use focused ultrasound to make the microbubbl­es vibrate in those specific areas, which temporaril­y opens the blood-brain barrier . The next step is injecting therapeuti­cs into the bloodstrea­m, which will get to those targeted areas. After treatment, the bloodbrain barrier closes up again within a few hours.

Aubert says this minimally invasive technique can be used to help treat any condition that requires a therapeuti­c to get into the brain or spinal cord more efficientl­y. Her research focuses on Alzheimer’s and she also collaborat­es with scientists working on Parkinson’s, ALS and stroke.

Aubert’s work in mouse models of Alzheimer’s has shown that delivering antibodies to the brain via focused ultrasound reduces amyloid-beta plaques, a hallmark of Alzheimer’s. She’s also found that increasing the permeabili­ty of the blood-brain barrier using focused ultrasound and microbubbl­es alone reduces these plaques and stimulates the growth of new neurons. “The learning and memory function of those mice was improved,” she said.

Clinical trials conducted by researcher­s at Sunnybrook and other institutio­ns have also found that it’s safe to use focused ultrasound on patients with Alzheimer’s and other neurodegen­erative disorders. The next step is doing clinical trials on therapeuti­cs delivered this way to see if they’re safe and effective, some of which are already underway.

One big concern with any therapeuti­c is how long it lasts, Aubert said. If you have a disease that lasts decades and the therapeuti­c only lasts days, you would need ongoing treatments. One potential solution could be gene therapy, which modifies a person’s genes to treat disease.

“It could be revolution­ary in terms of having one treatment for a lifetime of benefit,” Aubert said.

Medicine by Design has given Aubert and four other scientists from different discipline­s and institutio­ns more than $1 million to investigat­e this possibilit­y. “No one individual working in their own lab has all the answers,” Sefton said. “We bring together creative people working on novel ideas that will transform how we think about both disease and health.”

Reprogramm­ing the brain

Cindi Morshead, a professor and the chair of the division of anatomy in the department of surgery at the University of Toronto, is leading the Medicine by Design team that’s working on gene therapy to treat neurodegen­erative disorders.

“When you lose neurons, there’s no way to replace them and you have impaired functionin­g, so we want to try to make new neurons in the brain,” she said.

To do this, the researcher­s are converting astrocytes, a type of brain cell, into neurons. Astrocytes have many important functions — they keep the brain in a state of equilibriu­m, for instance — but they are far more abundant than neurons and can become toxic in some neurodegen­erative disorders, killing even more neurons. “By converting them, it’s kind of a doublewham­my,” Morshead said.

To reprogram brain cells, Morshead and her colleagues are designing novel genes that make neurons and deliver them to astrocytes. To ensure these genes get to the right parts of the brain, they’re using focused ultrasound, which is where Aubert’s expertise comes in.

This innovative treatment could halt the progressio­n or reverse the effects of neurodegen­erative disorders. A stroke patient could fully smile again after experienci­ng facial paralysis. An ALS patient could ski again after experienci­ng weakness in their legs. And an Alzheimer’s patient could remember the names of their children and grandchild­ren again after experienci­ng memory loss. “These people currently have no cure, only care,” Morshead said. “We’d offer hope to people who literally have no hope.”

Working with rodent models of stroke, Morshead and her colleagues have already found that their gene therapy leads to more neurons in the animals’ brains and helps them recover. After treatment, the rodents walk better — they don’t slip or drag their feet as much as before. If and when people can receive this treatment, they may see similar improvemen­ts. “For a stroke-injured patient, being able to regain the function to be able to pick up a utensil so they can feed themselves would have a huge impact on their quality of life,” Morshead said.

Aubert says people may be able to receive certain therapeuti­cs via focused ultrasound within years — even months in the case of antibodies for Alzheimer’s — but she and Morshead agree it will be decades before people can receive the gene therapy via focused ultrasound that they’re working on. There’s still much work to be done and questions to be answered.

For Aubert, the ultimate goal is to help as many people as possible live long, healthy and happy lives like her grandma.

“It’s a collective effort that will make it happen,” she said. “I’m optimistic.”

 ?? KEVIN VAN PAASSEN SUNNYBROOK ?? Kate Noseworthy is working with Isabelle Aubert at Sunnybrook Research Institute to develop a method of delivering therapeuti­cs to specific areas of the brain.
KEVIN VAN PAASSEN SUNNYBROOK Kate Noseworthy is working with Isabelle Aubert at Sunnybrook Research Institute to develop a method of delivering therapeuti­cs to specific areas of the brain.
 ?? KEVIN VAN PAASSEN SUNNYBROOK ?? Toronto scientist Isabelle Aubert, seen here in her lab at the Sunnybrook Research Institute pre-pandemic, is working on treatments to protect the brain and repair it after illness or injury.
KEVIN VAN PAASSEN SUNNYBROOK Toronto scientist Isabelle Aubert, seen here in her lab at the Sunnybrook Research Institute pre-pandemic, is working on treatments to protect the brain and repair it after illness or injury.

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