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Ginger improves cognitive function via NGF-induced ERK/CREB activation in the hippocampus of the mouse

Authors
Lim, SoonminMoon, MinhoOh, HyeinKim, Hyo GeunKim, Sun YeouOh, Myung Sook
Issue Date
Oct-2014
Publisher
ELSEVIER SCIENCE INC
Keywords
Leaning and memory; Zingiber officinale; Ginger; NGF; ERK/CREB; Synaptogenesis
Citation
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, v.25, no.10, pp.1058 - 1065
Journal Title
JOURNAL OF NUTRITIONAL BIOCHEMISTRY
Volume
25
Number
10
Start Page
1058
End Page
1065
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/12246
DOI
10.1016/j.jnutbio.2014.05.009
ISSN
0955-2863
Abstract
Ginger (the rhizome of Zingiber officinale Roscoe) has been used worldwide for many centuries in cooking and for treatment of several diseases. The main pharmacological properties of ginger include anti-inflammatory, antihyperglycemic, antiarthritic, antiemetic and neuroprotective actions. Recent studies demonstrated that ginger significantly enhances cognitive function in various cognitive disorders as well as in healthy brain. However, the biochemical mechanisms underlying the ginger-mediated enhancement of cognition have not yet been studied in normal or diseased brain. In the present study, we assessed the memory-enhancing effects of dried ginger extract (GE) in a model of scopolamine-induced memory deficits and in normal animals by performing a novel object recognition test. We found that GE administration significantly improved the ability of mice to recognize novel objects, indicating improvements in learning and memory. Furthermore, to elucidate the mechanisms of GE-mediated cognitive enhancement, we focused on nerve growth factor (NGF)-induced signaling pathways. NGF enzyme-linked immunosorbent assay analysis revealed that GE administration led to elevated NGF levels in both the mouse hippocampus and rat glioma C6 cells. GE administration also resulted in phosphorylation of extracellular-signal-regulated kinase (ERK) and cyclic AMP response element-binding protein (CREB), as revealed by Western blotting analysis. Neutralization of NGF with a specific NGF antibody inhibited GE-triggered activation of ERK and CREB in the hippocampus. Also, GE treatment significantly increased pre- and postsynaptic markers, synaptophysin and PSD-95, which are related to synapse formation in the brain. These data suggest that GE has a synaptogenic effect via NGF-induced ERK/CREB activation, resulting in memory enhancement. (C) 2014 Elsevier Inc. All rights reserved.
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