Ampelopsis Radix Protects Dopaminergic Neurons against 1-Methyl-4-phenylpyridinium/1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-Induced Toxicity in Parkinson’s Disease Models In Vitro and In Vivo

• Published in: Evidence-based complementary and alternative medicine Vol. 2013; no. 2013; pp. 1 - 9
• Main Authors: Park, Hanbyeol, Shim, Jin Sup, Kim, Hyo Geun, Lee, Hyejung, Oh, Myung Sook
• Format: Journal Article
• Language: English
• Published: Cairo, Egypt Hindawi Puplishing Corporation 01.01.2013; Hindawi Publishing Corporation; Hindawi Limited
• Subjects: 8-Hydroxydeoxyguanosine; Alzheimer's disease; Ampelopsis; Animal models; Antioxidants; Brain; Brain research; Colorimetry; Dopamine; Dopamine receptors; Free radicals; Herbal medicine; Hydroxylase; Immunohistochemistry; Metabolism; Metabolites; Movement disorders; MPTP; Neurodegeneration; Neurodegenerative diseases; Neuroprotection; Neurotoxicity; Oxidative stress; Parkinson's disease; Reactive oxygen species; Toxicity; United States > US; South Korea
• ISSN: 1741-427X; 1741-4288
• DOI: 10.1155/2013/346438

Ampelopsis Radix, the root of Ampelopsis japonica (Thunb.) Makino (Vitaceae), is a herbal medicine which has been widely used in East Asia. The present study was done to explore whether the standardized extract of Ampelopsis Radix (AJW) protects dopaminergic neurons via antioxidant mechanisms in Parkinson’s disease (PD) models. The effects of AJW on primary mesencephalic cultures stressed with 1-methyl-4-phenylpyridinium were investigated using tyrosine hydroxylase (TH) immunohistochemistry and reactive oxygen species measurement. The eliminative effects of AJW on the 2,2-diphenyl-1-picrylhydrazyl and 2,2′-azino-bis-(3-ethylbenzthiazoline-6-sulphonic acid) radicals were explored using colorimetric methods. The effects of AJW on the mice treated with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) were determined by pole test as well as TH and 8-hydroxydeoxyguanosine immunohistochemistry. AJW protected dopaminergic neurons by inhibiting reactive oxygen species generation in vitro. Moreover, AJW showed potent radical scavenging activities in vitro. In the mouse PD model, AJW protected the dopaminergic neurons in the brain, leading to motor improvements. AJW inhibited the MPTP-evoked accumulation of 8-hydroxydeoxyguanosine in the brain. These data suggest that AJW has neuroprotective effects with antioxidant mechanisms in PD models.