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http://dx.doi.org/10.20307/nps.2016.22.3.187

Effects of Gypenosides on Dopaminergic Neuronal Cell Death in 6-Hydroxydopamine-lesioned Rat Model of Parkinson's Disease with Long-term L-DOPA Treatment  

Shin, Keon Sung (College of Pharmacy and Research Center for Bioresource and Health, Chungbuk National University)
Zhao, Ting Ting (College of Pharmacy and Research Center for Bioresource and Health, Chungbuk National University)
Park, Hyun Jin (College of Pharmacy and Research Center for Bioresource and Health, Chungbuk National University)
Kim, Kyung Sook (College of Pharmacy and Research Center for Bioresource and Health, Chungbuk National University)
Choi, Hyun Sook (Department of Food and Nutrition, Chungcheong University)
Lee, Myung Koo (College of Pharmacy and Research Center for Bioresource and Health, Chungbuk National University)
Publication Information
Natural Product Sciences / v.22, no.3, 2016 , pp. 187-192 More about this Journal
Abstract
The goal of this study was to determine whether gypenosides (GPS) exert protective effects against dopaminergic neuronal cell death in a 6-hydroxydopamine (OHDA)-lesioned rat model of Parkinson's disease (PD) with or without long-term 3,4-dihydroxyphenylalanine (L-DOPA) treatment. Rats were injected with 6-OHDA in the substantia nigra to induce PD-like symptoms; 14 days after injection, groups of 6-OHDA-lesioned animals were treated for 21 days with GPS (25 or 50 mg/kg) and/or L-DOPA (20 mg/kg). Dopaminergic neuronal cell death was assessed by counting tyrosine hydroxylase (TH)-immunopositive cells in the substantia nigra and measuring levels of dopamine, norepinephrine, 3,4-dihydroxyphenylacetic acid (DOPAC), and homovanillic acid (HVA) in the striatum. Dopaminergic neuronal cell death induced by 6-OHDA lesions was ameliorated by GPS treatment (50 mg/kg). L-DOPA treatment exacerbated 6-OHDA-induced dopaminergic neuronal cell death; however, these effects were partially reversed by GPS treatment (25 and 50 mg/kg). These results suggest that GPS treatment is protective against dopaminergic neuronal cell death in a 6-OHDA-lesioned rat model of PD with long-term L-DOPA treatment. Therefore, GPS may be useful as a phytotherapeutic agent for the treatment of PD.
Keywords
Gypenosides; 6-Hydroxydopamine-lesioned rat; Parkinson's disease; Tyrosine hydroxylase immunohistochemistry; L-DOPA;
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