Scientists identify mechanism for brain dysfunction following seizures and drugs that prevent this impairment from occurring.
Six years ago, Cam Teskey, PhD, decided to follow a hunch. Armed with an advanced new tool designed to measure oxygen levels in tissues, he wanted to look at the brains of rats to see what was happening during seizures. Continue reading
Have you ever met someone who just wasn’t into music? They may have a condition called specific musical anhedonia, which affects three-to-five per cent of the population.
Researchers at the University of Barcelona and the Montreal Neurological Institute and Hospital of McGill University have discovered that people with this condition showed reduced functional connectivity between cortical regions responsible for processing sound and subcortical regions related to reward.
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Drug shown to reduce new attacks/symptom progression in some patients
In separate clinical trials, a drug called ocrelizumab has been shown to reduce new attacks in patients with relapsing remitting multiple sclerosis (MS), and new symptom progression in primary progressive MS.
Three studies conducted by an international team of researchers, which included Amit Bar-Or and Douglas Arnold from the Montreal Neurological Institute and Hospital of McGill University, have discovered that ocrelizumab can significantly reduce new attacks in patients with relapsing MS, as well as slow the progression of symptoms caused by primary progressive MS. Continue reading
Intellectual disability is characterized by significant impairment of cognitive and adaptive functions and affects 1-3 in 100 individuals worldwide. A few years ago, scientists at CHU Ste.Justine reported for the first time that genetic mutations in the gene SYNGAP1 cause a form of intellectual disability, which is often associated with autism spectrum disorders and epilepsy. Since then, DNA sequencing of SYNGAP1 in several groups of individuals with intellectual disability in Canada, the US and Europe has revealed that pathogenic mutations in SYNGAP1 are one of the most common cause of genetic intellectual disability. Continue reading
Scientists at McMaster University’s Stem Cell and Cancer Research Institute in collaboration with Sick Children’s Hospital have discovered genetic alterations in the gene DIXDC1 in individuals with autism spectrum disorders (ASD). This gene was found to change the way brain cells grow and communicate.
This finding, published today in Cell Reports, provides new insights into ASD that will guide identification of new medications for people with ASD. This is critical because ASD affects one in 68 individuals, and there are no medications that target the core symptoms of this complex disorder. Continue reading
It is known that neurodegenerative diseases such as Parkinson’s cause the gradual death of brain neurons. But what exactly are the mechanisms that go awry to cause degeneration of nerve cells? A team of researchers from Université Laval and the Quebec Mental Health Research Institute investigated the matter and show, in an article in Proceedings of the National Academy of Sciences (PNAS), the role played by two key regulatory proteins in the cascade of reactions leading to the death of neurons in Parkinson’s disease. Continue reading
3D depth-sensing camera shown to measure walking difficulties
A commonly used device found in living rooms around the world could be a cheap and effective means of evaluating the walking difficulties of multiple sclerosis (MS) patients.
The Microsoft Kinect is a 3D depth-sensing camera used in interactive video activities such as tennis and dancing. It can be hooked up to an Xbox gaming console or a Windows computer.
A team of researchers led by McGill University postdoctoral fellow Farnood Gholami, supervised by Jozsef Kövecses from the Department of Mechanical Engineering and Centre for Intelligent Machines, collaborated with Daria Trojan, a physiatrist in the Department of Neurology and Neurosurgery working at the Montreal Neurological Institute and Hospital, to test whether the Kinect could detect the differences in gait of MS patients compared to healthy individuals. Continue reading
Study confirms the existence of a molecular transport mechanism involved in fragile X syndrome
A team from the Centre de recherche de l’Institut universitaire en santé mentale de Québec– Université Laval has furthered our understanding of fragile X syndrome, the leading genetic cause of mental retardation in children. The article published by these researchers in a recent issue of PLoS Genetics confirms the model developed over 14 years by the team of Professor Edward Khandjian, and reveals new elements. Continue reading
Discovery could lead to ways to mitigate effects of jet lag and shift work
The brain’s biological clock stimulates thirst in the hours before sleep, according to a study published in the journalNature by McGill University researchers.
The finding — along with the discovery of the molecular process behind it — provides the first insight into how the clock regulates a physiological function. And while the research was conducted in mice, “the findings could point the way toward drugs that target receptors implicated in problems that people experience from shift work or jet lag,” Continue reading
Researchers find a mechanism that allows the brain to reconfigure connections between neurons in mere minutes.
A team from the Quebec Mental Health Institute – Université Laval has discovered a mechanism that allows the brain to rapidly reconfigure connections between its neurons. According to the researchers, whose findings were published in a recent issue of the journal Nature Communications, this mechanism plays a central role in brain plasticity. Continue reading