Neural Regeneration Research ›› 2021, Vol. 16 ›› Issue (11): 2219-2221.doi: 10.4103/1673-5374.310686

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Alpha-synuclein preformed fibrils: a tool to understand Parkinson’s disease and develop disease modifying therapy

Piotr Chmielarz, Andrii Domanskyi   

  1. Institute of Biotechnology, HiLIFE, University of Helsinki, Finland (Chmielarz P, Domanskyi A)
    Maj Institute of Pharmacology, Polish Academy of Sciences, Department of Brain Biochemistry, Kraków, Poland (Chmielarz P)
    Orion Corporation Orion Pharma, Turku, Finland (Domanskyi A)
  • Online:2021-11-15 Published:2021-04-13
  • Contact: Andrii Domanskyi, PhD, andrii.domanskyi@helsinki.fi.
  • Supported by:
    The present work was supported by grants from the Academy of Finland #293392, #319195; and Päivikki and Sakari Sohlberg Foundation (to AD); and Polish National Science Centre grant 2019/35/D/NZ7/03200 - Sonata 15 (to PC).

Abstract: Parkinson’s disease (PD) is the second most common neurodegenerative disorder characterized by multiple motor and non-motor symptoms, which include, among others, constipation, sleep disturbance, bradykinesia, gait and balance abnormalities, muscle stiffness and resting tremor. The motor symptoms are caused by progressive age-related death of dopaminergic neurons and in the vast majority of patients suffering from age-related idiopathic PD the cause of dopaminergic neurodegeneration is unknown. Even in the familial early-onset PD where genetic mutations have been identified, the molecular mechanisms driving degeneration of dopaminergic neurons are far from clear. Consequently, there is no clinically approved disease-modifying therapy capable of stopping or at least slowing down the disease progression.