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L-DOPA neurotoxicity is prevented by neuroprotective effects of erythropoietin

Title
L-DOPA neurotoxicity is prevented by neuroprotective effects of erythropoietin
Author
이영주
Keywords
L-DOPA; Erythropoietin; Phosphatidylinositol 3-kinase; Neurotoxicity
Issue Date
2011-12
Publisher
Elsevier Science B.V., Amsterdam.
Citation
Neurotoxicology December 2011 32(6):879-887
Abstract
The neurotoxicity of L-3,4-dihydroxyphenylalanine (L-DOPA), one of the most important drugs for the treatment of Parkinson's disease, still remains controversial, although much more data on L-DOPA neurotoxicity have been presented. Considering the well known neuroprotective effects of erythropoietin (EPO), the inhibitory effects of EPO on L-DOPA neurotoxicity need to be evaluated. Neuronally differentiated PC12 (nPC12) cells were treated with different concentrations of L-DOPA and/or EPO for 24 h. Cell viability was evaluated using trypan blue, 4',6-diamidino-2-phenylindole (DAPI) and TUNEL staining, and cell counting. Free radicals and intracellular signaling protein levels were measured with 2',7'-dichlorodihydrofluorescein diacetate (DCFH-DA) and Western blotting, respectively. L-DOPA reduced nPC12 cell viability at higher concentrations, but combined treatment with EPO and L-DOPA significantly restored cell viability. Free radicals and hydroxyl radical levels increased by L-DOPA were decreased after combined treatment of L-DOPA and EPO. Levels of survival-related intracellular signaling proteins decreased in nPC12 cells treated with 200 mu M L-DOPA but increased significantly in cells treated with 200 mu M L-DOPA and 5 mu M EPO. However, cleaved caspase-3, a death-related protein, increased in nPC12 cells treated with 200 mu M L-DOPA but decreased significantly in cells treated with 200 mu M L-DOPA and 5 mu M EPO. Pretreatment with LY294002, a phosphatidylinositol 3-kinase inhibitor, prior to combined treatment with EPO and L-DOPA almost completely blocked the protective effects of EPO. These results indicate that EPO can prevent L-DOPA neurotoxicity by activating the PI3K pathway as well as reducing oxidative stress. (C) 2011 Elsevier Inc. All rights reserved.
URI
https://www.sciencedirect.com/science/article/pii/S0161813X11000982http://hdl.handle.net/20.500.11754/66044
ISSN
0161-813X
DOI
10.1016/j.neuro.2011.05.009
Appears in Collections:
COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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