رژیم ورزش شدید به پیشرفت آهسته بیماری کمک می کند

Paolo Calabresi, the Full Professor of Neurology at the Catholic University and Director of the UOC Neurology at the University Polyclinic A. Gemelli IRCCS, said: “We have discovered a never observed mechanism, through which exercise performed in the early stages of the disease induces beneficial effects on movement control that may last over time even after training is suspended.” He added that this finding could guide the development of new non-drug treatments to be used alongside existing drug therapies.

Previous Knowledge and New Evidence

Previous research had indicated that intensive physical activity was linked to increased production of a vital growth factor, the brain-derived neurotrophic factor (BDNF). The authors successfully replicated this phenomenon using a four-week treadmill training protocol in an animal model of early-stage Parkinson’s disease. They demonstrated, for the first time, how this neurotrophic factor contributes to the beneficial effects of physical activity on the brain.

Investigating the Neuroprotective Effect

The study, led by Drs. Gioia Marino and Federica Campanelli, researchers at the Faculty of Medicine, Catholic University, Rome, lends experimental support to the neuroprotective effect of exercise. They employed a multidisciplinary approach using different techniques to measure improvements in neuronal survival, brain plasticity, motor control, and visuospatial cognition.

A key observation was that daily treadmill training sessions reduced the spread of pathological alpha-synuclein aggregates. In Parkinson’s disease, these aggregates cause gradual and progressive dysfunction of neurons in specific brain areas (the substantia nigra pars compacta and the striatum – constituting the so-called nigrostriatal pathway) essential to motor control.

Understanding the Biological Mechanism

The neuroprotective effect of physical activity is associated with the survival of neurons that release the neurotransmitter dopamine. This survival is crucial for striatal neurons’ ability to express a form of dopamine-dependent plasticity, which is otherwise impaired by the disease. Consequently, motor control and visuospatial learning, both dependent on nigrostriatal activity, are preserved in animals undergoing intensive training.

The study also revealed that BDNF, whose levels rise with exercise, interacts with the NMDA receptor for glutamate. This interaction enables neurons in the striatum to respond effectively to stimuli, with effects that endure beyond the exercise period.

Looking to the Future

Professor Paolo Calabresi said: “Our research team is involved in a clinical trial to test whether intensive exercise can identify new markers to monitor the disease progression slowing in early-stage patients and the profile of the progression of the disease. As Parkinson’s disease is characterized by important neuroinflammatory and neuroimmune components, which play a key role in the early stages of the disease, the research will keep on investigating the involvement of glial cells, highly specialized groups of cells that provide physical and chemical support to neurons and their environment. This will allow us to identify molecular and cellular mechanisms underlying the observed beneficial effects,” he concluded.

Reference: “Intensive exercise ameliorates motor and cognitive symptoms in experimental Parkinson’s disease restoring striatal synaptic plasticity” by Gioia Marino, Federica Campanelli, Giuseppina Natale, Maria De Carluccio, Federica Servillo, Elena Ferrari, Fabrizio Gardoni, Maria Emiliana Caristo, Barbara Picconi, Antonella Cardinale, Vittorio Loffredo, Francesco Crupi, Elvira De Leonibus, Maria Teresa Viscomi, Veronica Ghiglieri and Paolo Calabresi, 14 July 2023, Science Advances.
DOI: 10.1126/sciadv.adh1403