Science Daily
Accounting for sex differences in research animals is vital for the development of better treatments as drug shows promise in female mice alone
Date: September 11, 2019
Source: University of Toronto
Summary: Study finds that the diabetes drug metformin, known to promote brain repair, can also help restore cognitive function in adult mice but only in females and in a way that is dependent on the sex hormone estradiol.
Males are straightforward while females are complicated. This false dichotomy prompted a decades-long exclusion of female animals from research out of fear that their fluctuating hormone levels will muddle the data. But now a new study by Toronto scientists shows that a female sex hormone plays a key role in promoting brain repair and opens the door to the development of more effective treatments.
A team of researchers led by Cindi Morshead, a professor in the Donnelly Centre for Cellular and Biomolecular Research, found that metformin, a widely prescribed drug to treat diabetes, promotes repair in adult female brains and is dependent on the sex hormone estradiol.
Their findings are described in a study to be published in the September 11, 2019, issue of the journal Science Advances.
The research builds on a previous study, in collaboration with Freda Miller's group at the Hospital for Sick Children in Toronto, which sought to find treatment for childhood brain injury. They found that the widely prescribed drug metformin can induce brain repair and improve motor function in newborn mice that had a stroke. Metformin works by activating stem cells in the brain, which can self-renew and give rise to different types of brain cells to replace those killed by injury.
Because brain injury in early life can lead to lifelong cognitive problems, the researchers now wanted to find out if metformin also promoted cognitive recovery.
"You can fix a hole in someone's brain but if they don't function better it's irrelevant to them," says Morshead.
Graduate student Rebecca Ruddy induced stroke in newborn mice, followed by daily metformin treatment before the animals were tested in a puzzle box test that measured learning and memory.
To the researchers' delight, metformin was able to activate neural stem cells in the brain and promote cognitive recovery. But the data also revealed something unexpected. Metformin did not affect all the animals in equal manner. It only worked in adult females.
"When we first looked at the data, we did not see the benefit of the metformin treatment," says Morshead. "Then we noticed that adult females tended to do better than the males."
A closer look revealed that metformin selectively activated the adult female neural stem cells while having no effect on the males. This turned out to be due to the female sex hormone estradiol which somehow enhances the stem cells' ability to respond to metformin. Conversely, the male hormone testosterone appears to inhibit this process. When female mice had their ovaries removed and lacked the female sex hormone, the stem cells did not respond to metformin treatment.
"To know that there are both age and sex dependent effects -- it has such implications for treatment and therapeutics," says Morshead.
The findings come at a time when scientists are reckoning with the data bias that is skewed against women due to the predominant use of male animals in research.
"The thinking was that we're going to study males because everything you need to know is found in the male brain, and then the female brain just complicates things with hormones," says Morshead. "It's very misguided and troublesome for advancing neurological health."
As animal research informs human studies, the sex bias is believed to have led to failed clinical trials, misdiagnosis and inappropriate therapies for women, as highlighted in a recent article in Science.
Human trials of repurposing metformin as a brain repair drug are ongoing, with a pilot study testing it in children who suffered brain injury, led by Morshead's collaborators Dr. Donald Mabbott and Dr. Eric Bouffet, Head of Neurosciences and Mental Health Program and Director of Brain Tumour Programs, respectively, at SickKids. Although the current patient cohort is too small to detect any sex effects, the plan is to increase the number of patients to see if sex also affects treatment outcome in people, said Morshead.
The research was supported by the funding from the Canadian Institutes of Health Research, which in 2016 mandated its grant holders to account for sex dependent differences in animal research, as well as from the Ontario Institute for Regenerative Medicine, Medicine by Design, Brain Canada, the Stem Cell Network and the Ontario Brain Institute.
Story Source:
Materials provided by University of Toronto. Original written by Jovana Drinjakovic. Note: Content may be edited for style and length.
Journal Reference:
Rebecca M. Ruddy, Kelsey V. Adams, Cindi M. Morshead. Age- and sex-dependent effects of metformin on neural precursor cells and cognitive recovery in a model of neonatal stroke. Science Advances, 2019; 5 (9): eaax1912 DOI: 10.1126/sciadv.aax1912
Accounting for sex differences in research animals is vital for the development of better treatments as drug shows promise in female mice alone
Date: September 11, 2019
Source: University of Toronto
Summary: Study finds that the diabetes drug metformin, known to promote brain repair, can also help restore cognitive function in adult mice but only in females and in a way that is dependent on the sex hormone estradiol.
Males are straightforward while females are complicated. This false dichotomy prompted a decades-long exclusion of female animals from research out of fear that their fluctuating hormone levels will muddle the data. But now a new study by Toronto scientists shows that a female sex hormone plays a key role in promoting brain repair and opens the door to the development of more effective treatments.
A team of researchers led by Cindi Morshead, a professor in the Donnelly Centre for Cellular and Biomolecular Research, found that metformin, a widely prescribed drug to treat diabetes, promotes repair in adult female brains and is dependent on the sex hormone estradiol.
Their findings are described in a study to be published in the September 11, 2019, issue of the journal Science Advances.
The research builds on a previous study, in collaboration with Freda Miller's group at the Hospital for Sick Children in Toronto, which sought to find treatment for childhood brain injury. They found that the widely prescribed drug metformin can induce brain repair and improve motor function in newborn mice that had a stroke. Metformin works by activating stem cells in the brain, which can self-renew and give rise to different types of brain cells to replace those killed by injury.
Because brain injury in early life can lead to lifelong cognitive problems, the researchers now wanted to find out if metformin also promoted cognitive recovery.
"You can fix a hole in someone's brain but if they don't function better it's irrelevant to them," says Morshead.
Graduate student Rebecca Ruddy induced stroke in newborn mice, followed by daily metformin treatment before the animals were tested in a puzzle box test that measured learning and memory.
To the researchers' delight, metformin was able to activate neural stem cells in the brain and promote cognitive recovery. But the data also revealed something unexpected. Metformin did not affect all the animals in equal manner. It only worked in adult females.
"When we first looked at the data, we did not see the benefit of the metformin treatment," says Morshead. "Then we noticed that adult females tended to do better than the males."
A closer look revealed that metformin selectively activated the adult female neural stem cells while having no effect on the males. This turned out to be due to the female sex hormone estradiol which somehow enhances the stem cells' ability to respond to metformin. Conversely, the male hormone testosterone appears to inhibit this process. When female mice had their ovaries removed and lacked the female sex hormone, the stem cells did not respond to metformin treatment.
"To know that there are both age and sex dependent effects -- it has such implications for treatment and therapeutics," says Morshead.
The findings come at a time when scientists are reckoning with the data bias that is skewed against women due to the predominant use of male animals in research.
"The thinking was that we're going to study males because everything you need to know is found in the male brain, and then the female brain just complicates things with hormones," says Morshead. "It's very misguided and troublesome for advancing neurological health."
As animal research informs human studies, the sex bias is believed to have led to failed clinical trials, misdiagnosis and inappropriate therapies for women, as highlighted in a recent article in Science.
Human trials of repurposing metformin as a brain repair drug are ongoing, with a pilot study testing it in children who suffered brain injury, led by Morshead's collaborators Dr. Donald Mabbott and Dr. Eric Bouffet, Head of Neurosciences and Mental Health Program and Director of Brain Tumour Programs, respectively, at SickKids. Although the current patient cohort is too small to detect any sex effects, the plan is to increase the number of patients to see if sex also affects treatment outcome in people, said Morshead.
The research was supported by the funding from the Canadian Institutes of Health Research, which in 2016 mandated its grant holders to account for sex dependent differences in animal research, as well as from the Ontario Institute for Regenerative Medicine, Medicine by Design, Brain Canada, the Stem Cell Network and the Ontario Brain Institute.
Story Source:
Materials provided by University of Toronto. Original written by Jovana Drinjakovic. Note: Content may be edited for style and length.
Journal Reference:
Rebecca M. Ruddy, Kelsey V. Adams, Cindi M. Morshead. Age- and sex-dependent effects of metformin on neural precursor cells and cognitive recovery in a model of neonatal stroke. Science Advances, 2019; 5 (9): eaax1912 DOI: 10.1126/sciadv.aax1912