| Literature DB >> 27425033 |
Qi Hu1, Vladimir N Uversky2, Mengyang Huang3, Huicong Kang4, Feng Xu4, Xiaoyan Liu4, Lifei Lian4, Qiming Liang4, Hong Jiang1, Anding Liu5, Cuntai Zhang1, Francisco Pan-Montojo6, Suiqiang Zhu7.
Abstract
Parkinson's disease (PD) is a progressive neurodegenerative disease. α-Synuclein (α-syn) oligomers play a critical role in the progression of PD. Baicalein, a typical flavonoid compound, can inhibit the formation of the α-syn oligomers, and disaggregate existing α-syn oligomers in vitro. However, whether baicalein could inhibit or disaggregate α-syn oligomers in vivo has not been investigated. Therefore, this study was designed to investigate the inhibitory effects of baicalein on α-syn oligomers in vivo and to explore the possible mechanisms of such inhibition. A chronic PD mouse model was created by continuous intragastric administration of rotenone (5mg/kg, 12weeks). Baicalein (100mg/kg) was intraperitoneally injected from 7week to 12week. Our result showed that the amount of α-syn, changes in the levels of the striatal neurotransmitters, and the behavioral changes found in the chronic PD mouse model were prevented after the baicalein injections. Although baicalein did not decrease α-syn mRNA expression, α-syn oligomers were significantly decreased in the ileum, thoracic spinal cord, and midbrain. Furthermore, transmission electron microscopy analysis showed that baicalein could prevent α-syn monomers from the oligomer formation in vitro. Taken together, these results suggest that baicalein could prevent the progression of α-syn accumulation in PD mouse model partly by inhibiting formation of the α-syn oligomers.Entities:
Keywords: Baicalein; Flavonoid; Neurodegenerative disease; Parkinson's disease; Rotenone; α-Synuclein
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Year: 2016 PMID: 27425033 DOI: 10.1016/j.bbadis.2016.07.008
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002