Tag: University of Ottawa

  • The international research team’s ambitious work has implications across multiple fields and sheds compelling new light on the extraordinarily complex serotonin system.

    In our day-to-day lives, we’re constantly making a slew of decisions from immediate matters to prospects on the far horizon. But the evolutionary nuts-and-bolts of how our brains weigh these numerous daily decisions and what role is played by the neurotransmitter serotonin has been shrouded in mystery.

    Now, a new study led by an interdisciplinary uOttawa Faculty of Medicine team delivers fascinating findings on this big topic and potentially unravels a hidden aspect of what our nervous system’s complex serotonin system is really doing inside the enigmatic organ in our skulls.

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  • Source of text: David McFadden, Communications Advisor & Research Writer, University of Ottawa

    The study’s findings could potentially help develop targeted therapeutics for mood disorders like major depressive disorder.

    Our lives are filled with binary decisions – choices between one of two alternatives. But what’s really happening inside our brains when we engage in this kind of decision making?

    uOttawa Faculty of Medicine-led study published in Nature Neuroscience sheds new light on these big questions, illuminating a general principle of neural processing in a mysterious region of the midbrain that is the very origin of our central serotonin (5-HT) system, a key part of the nervous system involved in a remarkable range of cognitive and behavioral functions.

    “The current dominating model is that individual 5-HT neurons are acting independently one from another. While it had previously been suggested that 5-HT neurons may rather be connected with one another, it had not been directly demonstrated. That is what we did here. We also identify an intriguing processing role – or a computation – that is supported by this particular type of connectivity between 5-HT neurons,” says Dr. Jean-Claude Béïque, full professor in the Faculty’s Department of Cellular and Molecular Medicine and co-director of the uOttawa Brain and Mind Research Institute’s Centre for Neural Dynamics and Artificial Intelligence.

    The international research team’s work involved a mixture of several experimental approaches such as electrophysiology, cellular imaging, optogenetics and behavioral approaches, along with mathematical modeling and computer simulations.

    Forging advances

    So what does it mean that serotonin neurons clustered together in the brainstem are not independent actors largely keeping to themselves but are actually sending axons to the rest of the brain?

    “In my view, the paper’s main takeaway is that the mammalian serotonin system is far more anatomically and functionally complex than what we previously imagined. This is knowledge that could potentially help develop targeted therapeutics for mood disorders like major depressive disorder,” says Dr. Michael Lynn, the study’s first author and a former member of Dr. Béïque’s Faculty of Medicine lab.

    Dr. Lynn received his PhD in Neuroscience from the University of Ottawa in October 2023. He’s now working as a postdoctoral fellow at the University of Oxford, in the Department of Physiology, Anatomy and Genetics.

    He says the team’s findings are important because it turns out that there are distinct groups of serotonin neurons with their own activity patterns, each controlling serotonin release in a particular region of the brain. This has implications for the “winner-takes-all” principle of neuroscience – an idea applied in computational models of neural networks in which neurons essentially compete to get activated.

    “The new principles uncovered in this paper suggest that these distinct ensembles can interact in some scenarios: ‘winning’ serotonin ensembles with high activity can strongly reduce serotonin release from ‘losing’ serotonin ensembles with lower activity levels,” he says. “These imply a more complex, dynamic set of rules about how and when serotonin is released throughout the brain, contrasting with an older view of a more monolithic signal.”

    Decisions, decisions

    The research team’s work has implications for how our brain – an organ with profoundly intricate wiring of neurons with multitudes of enmeshed connections – is involved in day-to-day decision making.

    They determined how the lateral habenula, a region that is activated when we are frustrated and that is implicated in major depression, ultimately controls the activity of serotonin neurons. Habenular neurons are also believed to encode the level of threat that is perceived from a particular environment, or perhaps even from our actions.

    Dr. Béïque explains it like this: “Do we jump from the high diving board at the pool? Or only from the low one? Do we walk down that very dark alley, or do we avoid it?  When is dark too dark?  Somehow our brain must compute features of our world – including how threatening a particular environment is – and come up with a binary output: you go, or you don’t.”

    “We think we have identified a circuit that participates in that very computation that guides our everyday decisions,” he says.

    Next steps

    What’s next for the research team as they build on the advances they have forged over several years with this methodical, innovative examination of the serotonin system? They aim to focus on behavioral studies with mouse models.

    “At this point, the behavioral manifestations of the computation we discovered were somewhat artificial behavior. We’re currently trying to see if we can see similar things when mice are behaving in more naturalistic environments,” Dr. Béïque says.

    The talent-rich research team for the new Nature Neuroscience paper included the uOttawa Faculty of Medicine’sDr. Richard Naud, a computational neuroscientist who was the senior author on a recent serotonin-related study published in Nature, and Sean Geddes, director of Innovation and Partnerships at uOttawa.


  • New research could pave a way for pharmacological interventions for a devastating brain abnormality, announces a recent press release by the University of Ottawa.

    An international team led by Armen Saghatelyan, a newly appointed Canada Research Chair at the University of Ottawa’s Faculty of Medicine has shed light on the underlying mechanisms of a mysterious brain abnormality that occurs during human fetal development called Perfiventricula Heterotopia (abbreviated PH). PH is a neurodevelopmental affliction that is characterized by an abnormal migration of neuronal cells. These cells end up clustering around ventricles, the cavities of the brain. The disorder typically becomes apparent with recurrent seizures. 

    The collaborative research team led by Dr. Armen Saghatelyan aimed to uncover the migratory mechanisms of grafted human neuronal progenitor cells derived from PH patients in the brains of an immunodeficient mouse model. They wanted to test the hypothesis that changes in autophagy – a kind of cellular recycling process – impact the neuronal cells’ abnormal migratory behaviours.

    The team found that a drug called metformin restored the cells’ migratory properties by triggering autophagy.

    This discovery could potentially lead to the design of new strategies to better understand Periventricular heterotopia (PH) and treat this devastating disorder.

    The team’s findings were published recently in the journal EMBO Molecular Medicine. It was supported by a CIHR operating grant to Dr. Saghatelyan’s lab.

    Read the full press release on the eurekalert.org website.


  • Dr. Baptiste Lacoste wants to find out what’s going wrong with the blood vessels in the autistic brain. His team was the first to discover that these blood vessels don’t work properly in mouse models of autism, and there’s some cellular evidence that this happens in humans as well. Now, in a new study published in Cell Reports, the team has found that blood vessel problems in this mouse model cause the brain to absorb glucose at a much higher rate than a neurotypical brain, consistent with less efficient metabolism. Glucose is a sugar that the body uses for energy, and the blood vessels control how much glucose gets into the brain cells. The team also found that the cells lining these blood vessels (known as endothelial cells) have fewer mitochondria, the cell’s powerhouses, because a genetic switch that controls their production is missing. This problem in the blood vessels forces the brain to change the way it uses energy, which may be causing the behavioural changes seen in autism. Now that they’ve identified this problem, Dr. Lacoste’s team is looking to bring back this energy switch. Their preliminary findings, presented at recent scientific conferences, suggest this may help normalize function in the autistic brain.

    Original research article:

    Béland-Millar A, Kirby A, Truong Y, Ouellette J, Yandiev S, Bouyakdan K, Pileggi C, Naz S, Yin M, Carrier M, Kotchetkov P, St-Pierre MK, Tremblay MÈ, Courchet J, Harper ME, Alquier T, Messier C, Shuhendler AJ, Lacoste B. 16p11.2 haploinsufficiency reduces mitochondrial biogenesis in brain endothelial cells and alters brain metabolism in adult mice. Cell Rep. 2023 May 30;42(5):112485. doi: 10.1016/j.celrep.2023.112485. Epub 2023 May 6. PMID: 37149866.

    https://www.cell.com/cell-reports/fulltext/S2211-1247(23)00496-5


  • All humans require sleep daily to be physically and mentally healthy. Sleep is known to play a role in solidifying new memories and learning. However, researchers do not fully understand the processes in the brain that underlie the consolidation of newly acquired information and skills during sleep.

    With the support of a CIHR Fellowship, Dr. Dylan Smith from University of Ottawa Institute for Mental Health Research is combining electroencephalography (EEG) with functional magnetic resonance imaging (fMRI) to peer inside the brains of healthy volunteers and study these processes at work.

    Study participants are placed inside an MRI brain scanner wherein they are instructed to solve a visual puzzle before falling asleep. Dr. Smith is analyzing the data from these brain scans with a focus on sleep spindles – fast bursts of brain activity linked to sleep and memory – in parts of the brain associated with learning, such as the prefrontal cortex, hippocampus, and striatum. This research is providing new insight into how our brains integrate new learning while we’re sleeping.

    Learn more about the Faces of health research 2022 on the CIHR website.

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