Authors
S Pchelina, A Emelyanov, G Baydakova, P Andoskin, K Senkevich, M Nikolaev, I Miliukhina, A Yakimovskii, A Timofeeva, E Fedotova, N Abramycheva, T Usenko, D Kulabukhova, A Lavrinova, A Kopytova, L Garaeva, E Nuzhnyi, S Illarioshkin, E Zakharova
Publication date
2017/1/1
Journal
Neuroscience letters
Volume
636
Pages
70-76
Publisher
Elsevier
Description
Alpha-synuclein oligomerization plays a key role in the development of Parkinson’s disease (PD). Being the most common genetic contributor to PD, glucocerebrosidase 1 (GBA) mutations have been associated with decreased GBA enzymatic activity in PD patients with mutations in the GBA gene (GBA-PD). However, it is unknown whether the activities of other lysosomal hydrolases are being altered in GBA-PD patients and are accompanied by an increase in alpha-synuclein oligomerization.
The aim of our study was to estimate GBA enzymatic activity as well as the activities of five other lysosomal hydrolases (galactocerebrosidase, alpha-glucosidase, alpha-galactosidase, sphingomyelinase, alpha-iduronidase) in dried blood spots with assessing plasma oligomeric alpha-synuclein levels in sporadic PD (sPD) patients, in GBA-PD patients and in controls.
GBA enzymatic activity and plasma oligomeric alpha …
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