Abstract
Oxidative stress is one of the underlying causes of Parkinson’s disease (PD). Because of its antioxidant effect, we hypothesize that green tea consumption (3 cups daily for 3 months) would improve antioxidant status and reduces oxidative damage in Parkinson’s disease. Fifteen subjects who were within the first five years of PD, on stable PD medication, and not regular green tea consumers were recruited. Iron status, oxidative stress and PD status were evaluated before and after 3 months of green tea consumption. Hemoglobin, serum iron, iron saturation and ferritin concentrations were used to assess iron status. Antioxidant enzymes including catalase, superoxide dismutase (SOD), and glutathione peroxidase (GPx) were measured to determine antioxidant status. Lipid peroxidation and protein carbonyls were measured as oxidative damage markers. There were no changes in total motor scores of the Unified Parkinson’s Disease Rating Scale (UPDRS), PDQ-39 total scores and various iron status markers after 3 months. Catalase (p < 0.05) and SOD activities (p < 0.005) were increased significantly indicating an improvement of antioxidant status. Both lipid peroxidation and protein carbonyls decreased by ~52% (p < 0.01) with green tea consumption, indicating less oxidative stress. In conclusion, 3 cups of green tea consumption for 3 months can improve antioxidant status and reduce oxidative damage in PD patients. Further studies are needed to determine if these changes result in slowing the disease progression.
Highlights
Parkinson’s disease (PD) is a slowly progressive, and neurodegenerative disorder
The purpose of this study is to identify the beneficial effect of green tea consumption in PD patients
One subject was withdrawn during the study period due to noncompliance with tea drinking, data are provided for 14 subjects
Summary
Parkinson’s disease (PD) is a slowly progressive, and neurodegenerative disorder. Several factors, such as aging, How to cite this paper: Chen, D., Zhou, Y., Lyons, K.E., Pahwa, R. and Reddy, M.B. Among these factors, oxidative stress is critical in initiating and promoting neurodegeneration [1] [2]. Excess iron accumulation in the brain leads to free radical formation via the Fenton reaction, contributing to oxidation damage of lipids and protein and promoting cell death [3]. Significant elevation of iron has been reported in the substantia nigra of PD patients compared with age-matched controls [4] [5], indicating the critical role of iron in PD progression
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