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Effects of chronic low dose rotenone treatment on human microglial cells
by
Shaikh, Shamim B
, Nicholson, Louise FB
in
Biomedical and Life Sciences
/ Biomedicine
/ Brain
/ Disease
/ Experiments
/ Health aspects
/ Health sciences
/ Herbicides
/ Medical research
/ Molecular Medicine
/ Neurology
/ Neurons
/ Neurosciences
/ Nitric oxide
/ Pathogenesis
/ Physiological aspects
/ Research Article
/ Rodents
/ Standard deviation
/ Statistical analysis
/ Studies
2009
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Effects of chronic low dose rotenone treatment on human microglial cells
by
Shaikh, Shamim B
, Nicholson, Louise FB
in
Biomedical and Life Sciences
/ Biomedicine
/ Brain
/ Disease
/ Experiments
/ Health aspects
/ Health sciences
/ Herbicides
/ Medical research
/ Molecular Medicine
/ Neurology
/ Neurons
/ Neurosciences
/ Nitric oxide
/ Pathogenesis
/ Physiological aspects
/ Research Article
/ Rodents
/ Standard deviation
/ Statistical analysis
/ Studies
2009
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Do you wish to request the book?
Effects of chronic low dose rotenone treatment on human microglial cells
by
Shaikh, Shamim B
, Nicholson, Louise FB
in
Biomedical and Life Sciences
/ Biomedicine
/ Brain
/ Disease
/ Experiments
/ Health aspects
/ Health sciences
/ Herbicides
/ Medical research
/ Molecular Medicine
/ Neurology
/ Neurons
/ Neurosciences
/ Nitric oxide
/ Pathogenesis
/ Physiological aspects
/ Research Article
/ Rodents
/ Standard deviation
/ Statistical analysis
/ Studies
2009
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Effects of chronic low dose rotenone treatment on human microglial cells
Journal Article
Effects of chronic low dose rotenone treatment on human microglial cells
2009
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Overview
Background
Exposure to toxins/chemicals is considered to be a significant risk factor in the pathogenesis of Parkinson's disease (PD); one putative chemical is the naturally occurring herbicide rotenone that is now used widely in establishing PD models. We, and others, have shown that chronic low dose rotenone treatment induces excessive accumulation of Reactive Oxygen Species (ROS), inclusion body formation and apoptosis in dopaminergic neurons of animal and human origin. Some studies have also suggested that microglia enhance the rotenone induced neurotoxicity. While the effects of rotenone on neurons are well established, there is little or no information available on the effect of rotenone on microglial cells, and especially cells of human origin. The aim of the present study was to investigate the effects of chronic low dose rotenone treatment on human microglial CHME-5 cells.
Methods
We have shown previously that rotenone induced inclusion body formation in human dopaminergic SH-SY5Y cells and therefore used these cells as a control for inclusion body formation in this study. SH-SY5Y and CHME-5 cells were treated with 5 nM rotenone for four weeks. At the end of week 4, both cell types were analysed for the presence of inclusion bodies, superoxide dismutases and cell activation (only in CHME-5 cells) using Haematoxylin and Eosin staining, immunocytochemical and western blotting methods. Levels of active caspases and ROS (both extra and intra cellular) were measured using biochemical methods.
Conclusion
The results suggest that chronic low dose rotenone treatment activates human microglia (cell line) in a manner similar to microglia of animal origin as shown by others. However human microglia release excessive amounts of ROS extracellularly, do not show excessive amounts of intracellular ROS and active caspases and most importantly do not show any protein aggregation or inclusion body formation. Human microglia appear to be resistant to rotenone (chronic, low dose) induced damage.
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