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Ginsenoside Re and Rd Enhance the Expression of Cholinergic Markers and Neuronal Differentiation in Neuro-2a Cells

Authors
Kim, Min SooYu, Jung MinKim, Hee JungKim, Hae BokKim, Seung TaeJang, Su KilChoi, Young WookLee, Do IkJoo, Seong Soo
Issue Date
May-2014
Publisher
PHARMACEUTICAL SOC JAPAN
Keywords
ginsenoside; choline acetyltransferase; vesicular acetylcholine transporter; acetylcholine; Alzheimer's disease
Citation
BIOLOGICAL & PHARMACEUTICAL BULLETIN, v.37, no.5, pp 826 - 833
Pages
8
Journal Title
BIOLOGICAL & PHARMACEUTICAL BULLETIN
Volume
37
Number
5
Start Page
826
End Page
833
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/12262
DOI
10.1248/bpb.b14-00011
ISSN
0918-6158
1347-5215
Abstract
In Alzheimer's disease (AD), extensive neuronal loss and a deficiency of the neurotransmitter acetylcholine (ACh) are the major characteristics during pathogenesis in the brain. In the present study, we aimed to investigate whether representative ginsenosides from ginseng can regulate choline acetyltransferase (ChAT) and vesicular acetylcholine transporter (VAChT), which are required for cholinergic neurotransmission. Our results revealed that Re and Rd induced effectively the expression of ChAT/VAChT genes in Neuro-2a cells as well as ACh elevation. Microtubule-associated protein-2 (MAP-2), nerve growth factor receptor (p75), p21, and TrkA genes and proteins were also significantly expressed. Moreover, both activated extracelullar signal-regulated protein kinase (ERK) and Akt were inhibited by K252a, a selective Trk receptor inhibitor. These findings strongly indicate that Re and Rd play an important role in neuronal differentiation and the nerve growth factor (NGF)-TrkA signaling pathway. High performance liquid chromatography analysis showed that Re and Rd administered orally were transported successfully into brain tissue and increased the level of ChAT and VAChT mRNA. The present study demonstrates that Re and Rd are selective candidates for upregulation of the expression of cholinergic markers, which may counter the symptoms and progress of AD.
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