Mountain-cultivated ginseng protects against cognitive impairments in aged GPx-1 knockout mice via activation of Nrf2/ChAT/ERK signaling pathway

胆碱乙酰转移酶 谷胱甘肽过氧化物酶 MAPK/ERK通路 人参 基因剔除小鼠 人口 内分泌学 内科学 药理学 医学 化学 信号转导 生物 胆碱能的 细胞生物学 氧化应激 过氧化氢酶 受体 病理 环境卫生 替代医学
作者
Bao Trong Nguyen,Eun‐Joo Shin,Ji Hoon Jeong,Naveen Sharma,Ngoc Kim Cuong Tran,Yen Nhi Doan Nguyen,Dae-Joong Kim,Myung Bok Wie,Yi Lee,Jae Kyung Byun,Sung Kwon Ko,Seung-Yeol Nah,Hyoung‐Chun Kim
出处
期刊:Journal of Ginseng Research [Elsevier BV]
卷期号:47 (4): 561-571 被引量:3
标识
DOI:10.1016/j.jgr.2023.01.005
摘要

Escalating evidence shows that ginseng possesses an antiaging potential with cognitive enhancing activity. As mountain cultivated ginseng (MCG) is cultivated without agricultural chemicals, MCG has emerged as a popular herb medicine. However, little is known about the MCG-mediated pharmacological mechanism on brain aging.As we demonstrated that glutathione peroxidase (GPx) is important for enhancing memory function in the animal model of aging, we investigated the role of MCG as a GPx inducer using GPx-1 (a major type of GPx) knockout (KO) mice. We assessed whether MCG modulates redox and cholinergic parameters, and memory function in aged GPx-1 knockout KOmice.Redox burden of aged GPx-1 KO mice was more evident than that of aged wild-type (WT) mice. Alteration of Nrf2 DNA binding activity appeared to be more evident than that of NFκB DNA binding activity in aged GPx-1 KO mice. Alteration in choline acetyltransferase (ChAT) activity was more evident than that in acetylcholine esterase activity. MCG significantly attenuated reductions in Nrf2 system and ChAT level. MCG significantly enhanced the co-localization of Nrf2-immunoreactivity and ChAT-immunoreactivity in the same cell population. Nrf2 inhibitor brusatol significantly counteracted MCG-mediated up-regulation in ChAT level and ChAT inhibition (by k252a) significantly reduced ERK phosphorylation by MCG, suggesting that MCG might require signal cascade of Nrf2/ChAT/ERK to enhance cognition.GPx-1 depletion might be a prerequisite for cognitive impairment in aged animals. MCG-mediated cognition enhancement might be associated with the activations of Nrf2, ChAT, and ERK signaling cascade.

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