黑质
神经退行性变
鱼藤酮
粒体自噬
神经发生
酪氨酸羟化酶
内分泌学
内科学
自噬
神经科学
医学
生物
多巴胺
线粒体
细胞生物学
多巴胺能
细胞凋亡
生物化学
疾病
作者
Michael F. Almeida,Carolliny M. Silva,Rodrigo S. Chaves,Nathan C. R. Lima,Renato S. Almeida,Karla P. Melo,Marilene Demasi,Tiago Fernandes,Edilamar Menezes de Oliveira,Luís Eduardo Soares Netto,Sandra M. Cardoso,M Ferrari
标识
DOI:10.1080/02640414.2017.1378494
摘要
Moderate physical exercise acts at molecular and behavioural levels, such as interfering in neuroplasticity, cell death, neurogenesis, cognition and motor functions. Therefore, the aim of this study is to analyse the cellular effects of moderate treadmill running upon substantia nigra during early neurodegeneration. Aged male Lewis rats (9-month-old) were exposed to rotenone 1mg/kg/day (8 weeks) and 6 weeks of moderate treadmill running, beginning 4 weeks after rotenone exposure. Substantia nigra was extracted and submitted to proteasome and antioxidant enzymes activities, hydrogen peroxide levels and Western blot to evaluate tyrosine hydroxylase (TH), alpha-synuclein, Tom-20, PINK1, TrkB, SLP1, CRMP-2, Rab-27b, LC3II and Beclin-1 level. It was demonstrated that moderate treadmill running, practiced during early neurodegeneration, prevented the increase of alpha-synuclein and maintained the levels of TH unaltered in substantia nigra of aged rats. Physical exercise also stimulated autophagy and prevented impairment of mitophagy, but decreased proteasome activity in rotenone-exposed aged rats. Physical activity also prevented H2O2 increase during early neurodegeneration, although the involved mechanism remains to be elucidated. TrkB levels and its anterograde trafficking seem not to be influenced by moderate treadmill running. In conclusion, moderate physical training could prevent early neurodegeneration in substantia nigra through the improvement of autophagy and mitophagy.
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