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논문 기본 정보

자료유형
학술저널
저자정보
Hee Jin Kim (Sahmyook University) Min Yeong Lee (Sahmyook University) Gyu Ri Kim (Sahmyook University) Hyun Jun Lee (Sahmyook University) Leandro Val Sayson (Sahmyook University) Darlene Mae D. Ortiz (Sahmyook University) Jae Hoon Cheong (Jeonbuk National University) Mikyung Kim (Sahmyook University)
저널정보
고려인삼학회 Journal of Ginseng Research Journal of Ginseng Research Vol.47 No.4
발행연도
2023.7
수록면
583 - 592 (10page)

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초록· 키워드

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Background: Alcohol is one of the most commonly used psychoactive drugs. Due to its addictive characteristics, many people struggle with the side effects of alcohol. Korean Red Ginseng (KRG) is a traditional herbal medicine that is widely used to treat various health problems. However, the effects and mechanisms of KRG in alcohol-induced responses remain unclear. Therefore, the purpose of this study was to investigate the effects of KRG in alcohol-induced responses.
Methods: We investigated two aspects: alcohol-induced addictive responses and spatial working memory impairments. To determine the effects of KRG in alcohol-induced addictive responses, we performed conditioned place preference tests and withdrawal symptom observations. To assess the effects of KRG in alcohol-induced spatial working memory impairment, Y-maze, Barnes maze, and novel object recognition tests were performed using mice after repeated alcohol and KRG exposure. To investigate the potential mechanism of KRG activity, gas chromatography-mass spectrometry and western blot analysis were performed. Results: KRG-treated mice showed dose-dependent restoration of impaired spatial working memory following repeated alcohol exposure. Furthermore, withdrawal symptoms to alcohol were reduced in mice treated with KRG and alcohol. The PKA-CREB signaling pathway was activated after alcohol administration, which was reduced by KRG. However, the levels of inflammatory cytokines were increased by alcohol and decreased by KRG.
Conclusion: Taken together, KRG may alleviate alcohol-induced spatial working memory impairments and addictive responses through anti-neuroinflammatory activity rather than through the PKA-CREB signaling pathway.

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ABSTRACT
1. Introduction
2. Materials and methods
3. Results
4. Discussion
References

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