Oxidative stress involvement in manganese-induced alpha-synuclein oligomerization in organotypic brain slice cultures

• DOI: 10.1016/j.tox.2013.01.006
• Publication Date: 2013-01-23T09:22:57Z
• Authors: Bin Xu; Sheng-Wen Wu; Chun-Wei Lu; Yu Deng; Wei Liu; Yan-Gang Wei; Tian-Yao Yang; Zhao-Fa Xu
• Keywords: Brain Chemistry; Neurons; Manganese; 0303 health sciences; L-Lactate Dehydrogenase; Manganese Poisoning; Blotting, Western; Brain; Apoptosis; Hydrogen Peroxide; Real-Time Polymerase Chain Reaction; Glutathione; Basal Ganglia; Rats; Protein Carbonylation; Oxidative Stress; 03 medical and health sciences; Organ Culture Techniques; Animals; RNA; Rats, Wistar; Reactive Oxygen Species

Overexposure to manganese (Mn) has been known to induce neuronal damage. However, little is known of the role that reactive oxygen species (ROS) play in protein aggregation resulting from Mn exposure. The current study investigated whether oxidative stress is involved in manganese-induced alpha-synuclein oligomerization in organotypic brain slices. After application of Mn (0-400μM) for 24h, there was a dose-dependent increase in average percentage of propidium iodide positive (PI(+)) nuclei in slices and levels of lactate dehydrogenase (LDH) in the culture medium. Moreover, the treatment with Mn resulted in a dose-dependent increase in neurocyte apoptosis, ROS level, and decrease in superoxide dismutase (SOD) activity. Mn also caused oxidative damage in cell lipid and protein. At the same time, the exposure of Mn leaded to significantly increase in the expression of alpha-synuclein mRNA and protein. Alpha-synuclein oligomerization occurred in Mn-treated slices, especially on membrane-bound form. It indicated that alpha-synuclein oligomers were more likely to combination cell membranes and resulting in membrane damage. Mn-induced neurocyte damage and alpha-synuclein oligomerization were also partially alleviated by the pretreatment with GSH and aggravated by H2O2 pretreatment. The findings revealed Mn might exert its neurotoxic effects by oxidative stress-mediated alpha-synuclein oligomerization in organotypic brain slices.