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DA-9801, a standardized Dioscorea extract, improves memory function via the activation of nerve growth factor-mediated signaling

神经生长因子 奶油 MAPK/ERK通路 海马结构 神经突 神经科学 海马体 神经营养因子 内分泌学 内科学 生物 信号转导 细胞生物学 体外 医学 转录因子 受体 生物化学 基因
作者
Jin Gyu Choi,Zahra Khan,Sang-Zin Choi,Sun Yeou Kim,Myung Sook Oh
出处
期刊:Nutritional Neuroscience [Taylor & Francis]
卷期号:25 (2): 219-230 被引量:5
标识
DOI:10.1080/1028415x.2020.1743916
摘要

Nerve growth factor (NGF) is a neurotrophin that plays a critical role in mammalian learning and memory functions. NGF also regulates neuronal cell differentiation and neurite outgrowth by activating ERK/CREB signaling. This present study examined the effects of a standardized Dioscorea extract (DA-9801), which is composed of Dioscorea japonica Thunb and Dioscorea nipponica Makino on memory function via its NGF-potentiating activities using an in vitro and in vivo paradigm.Cells were incubated with or without different concentrations of DA-9801 (10, 25, and 50 μg/ml) extract for 24 h. The cultured conditioned medium from C6 glioma cells was used for NGF production assay, and neurite length in N2a cells was measured after every 2 h. Mice were orally treated with DA-9801 (10 and 100 mg/kg/day) once daily for 7 days. They were subjected to passive avoidance test to evaluate memory functions. The question of whether DA-9801 induced NGF synthesis was assessed by measuring the levels of NGF in the mouse cortical and hippocampal tissues. Hippocampal cell differentiation and NGF-mediated ERK/CREB signaling were evaluated by performing immunohistochemical analysis using BrdU, ki67, DCX, phosphorylated ERK and CREB in the mouse hippocampus.DA-9801 treatment increased the NGF contents and neurite length, respectively. Mice with DA-9801 administration showed memory enhancement in the passive avoidance test. DA-9801 also increased newborn cell differentiation, neurite length, NGF secretion, and ERK/CREB phosphorylation in the mouse hippocampus.These results suggest that DA-9801 treatment could improve memory function by inducing hippocampal NGF synthesis and ERK/CREB signaling.

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