Parkinson’s disease brain cells at risk of burnout, like an overheating motor

The findings are in some ways a culmination of Trudeau's 17 years of studying the part of the brain that causes Parkinson's disease, schizophrenia and drug addiction. His findings could open the door to the creation of better animal models of Parkinson's disease and the identification of new treatment strategies. "For some unknown reason, it has been incredibly difficult to reproduce the symptoms of Parkinson's in mice, even when introducing in the genome of these animals the same mutations found in humans afflicted by familial forms of the disease. Our discovery provides a new lead to potentially overcome such difficulties" Trudeau explained.

Improved animal models open a variety of new avenues of research. "It's possible that new medications could be developed to help the neurons in question reduce their energy consumption or produce energy more efficiently, which would reduce accumulated damage over the years," Trudeau said. His team is already looking at the possible next steps with Professor Slack and her colleague Professor David Park.

Targeting the dark side

Unlike Alzheimer's, which has a wider-ranging impact on billions of brain neurons, the primary symptoms or Parkinson's are caused by the death of tens or hundreds of thousands of neurons in a few more restricted areas of the brain, including regions called the substantia nigra (literally "the black substance"), the locus ceruleus and the dorsal nucleus of the vagus nerve.

Key to the mystery may be mitochondria, the powerhouses that allow cells to grow and neurons to conduct electrical signals and release their chemical messengers such as dopamine, noradrenaline and acetylcholine. For the past three years, the research team carried out numerous experiments in order to identify why mitochondria in neurons of the substantia nigra work so hard and apparently lead neurons to "overheat."

They discovered that this overheating could be caused by the fact that these neurons have an amazingly complex structure with a large number of extensions and neurotransmitter release sites, much like a tree with numerous branches. Providing energy to these numerous branches may make the neurons particularly vulnerable, leading, in the context of aging, to malfunction and cell death, thus triggering Parkinson's, with the onset of symptoms generally at around age sixty. "Our work supports the theory that very complex neurons like those found in the substantia nigra force the mitochondria to constantly work at burnout rates to produce energy. This would explain the accelerated cell deterioration," Trudeau explained. "To use the analogy of a motor, a car that overheats will burn significantly more fuel, and, not surprisingly, end up at the garage more often."

Professor Trudeau notes that the most common neurodegenerative diseases are particularly challenging for researchers, because in a way, their increasing prevalence is the result of increased life expectancy. "From an evolutionary standpoint, some of our neurons are perhaps just not programmed to last 80, 90 or 100 years, as we are seeing more and more. It's to be expected that certain parts of our body are less able to withstand the effects of time," he said. However, given the more localized nature of Parkinson's disease (compared to other afflictions), an effective treatment may be discovered in the not-too-distant future. Nevertheless, Trudeau points out that his primary goal is to develop a fundamental understanding of the mechanisms of the brain in order to shed new light on neurological disorders.