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Korean Red Ginseng reduces chronic social defeat stress-induced mood disorders via N-methyl-D-aspartate receptor modulation in mice

BACKGROUND: A chronic social defeat stress (CSDS) model has been proposed as relevant to stress-induced behavioral change in humans. In this study, we examined the effect of Korean Red Ginseng (KRG) on CSDS-induced mood disorders and protein expression in an animal model. METHODS: To evaluate the ef...

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Autores principales: Lee, Bo-Ram, Lee, Ju-Hyun, Ko, Yong-Hyun, Seo, Jee-Yeon, Hur, Kwang-Hyun, Kim, Young-Jung, Kim, Seon-Kyung, Kim, Seong-Eon, Lee, Seok-Yong, Jang, Choon-Gon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020286/
https://www.ncbi.nlm.nih.gov/pubmed/33841006
http://dx.doi.org/10.1016/j.jgr.2019.11.003
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author Lee, Bo-Ram
Lee, Ju-Hyun
Ko, Yong-Hyun
Seo, Jee-Yeon
Hur, Kwang-Hyun
Kim, Young-Jung
Kim, Seon-Kyung
Kim, Seong-Eon
Lee, Seok-Yong
Jang, Choon-Gon
author_facet Lee, Bo-Ram
Lee, Ju-Hyun
Ko, Yong-Hyun
Seo, Jee-Yeon
Hur, Kwang-Hyun
Kim, Young-Jung
Kim, Seon-Kyung
Kim, Seong-Eon
Lee, Seok-Yong
Jang, Choon-Gon
author_sort Lee, Bo-Ram
collection PubMed
description BACKGROUND: A chronic social defeat stress (CSDS) model has been proposed as relevant to stress-induced behavioral change in humans. In this study, we examined the effect of Korean Red Ginseng (KRG) on CSDS-induced mood disorders and protein expression in an animal model. METHODS: To evaluate the effect of KRG on social defeat stress, test mice were exposed in the resident aggressor's home cage compartment for 14 days beginning 1 h after KRG treatment (10, 20, and 40 mg/kg, per oral (p.o.)). After the exposure, behavioral tests to measure anxiety, social interaction, and depression-like behavior were performed. To investigate the underlying mechanism, N-methyl-D-aspartate receptor expression levels in CSDS-induced mice were evaluated using Western blot analysis. RESULTS: CSDS induced anxiety-like behaviors by decreasing central activity in the open-field test and open-arm approach in the elevated plus maze test and led to social avoidance behavior in the social interaction test. CSDS mice showed upregulated NR1, NR2A, and NR2B expression in the hippocampus. KRG 20 and 40 mg/kg ameliorated anxiety-like activities and KRG 20 mg/kg alleviated social avoidance by decreasing time in the corner zone. KRG treatment recovered CSDS-induced NR1, NR2A, and NR2B protein levels in the hippocampus. CONCLUSION: These results indicate that KRG has a therapeutic effect on CSDS-induced mood disorder by alleviating N-methyl-D-aspartate receptor overexpression in the hippocampus.
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spelling pubmed-80202862021-04-08 Korean Red Ginseng reduces chronic social defeat stress-induced mood disorders via N-methyl-D-aspartate receptor modulation in mice Lee, Bo-Ram Lee, Ju-Hyun Ko, Yong-Hyun Seo, Jee-Yeon Hur, Kwang-Hyun Kim, Young-Jung Kim, Seon-Kyung Kim, Seong-Eon Lee, Seok-Yong Jang, Choon-Gon J Ginseng Res Research Article BACKGROUND: A chronic social defeat stress (CSDS) model has been proposed as relevant to stress-induced behavioral change in humans. In this study, we examined the effect of Korean Red Ginseng (KRG) on CSDS-induced mood disorders and protein expression in an animal model. METHODS: To evaluate the effect of KRG on social defeat stress, test mice were exposed in the resident aggressor's home cage compartment for 14 days beginning 1 h after KRG treatment (10, 20, and 40 mg/kg, per oral (p.o.)). After the exposure, behavioral tests to measure anxiety, social interaction, and depression-like behavior were performed. To investigate the underlying mechanism, N-methyl-D-aspartate receptor expression levels in CSDS-induced mice were evaluated using Western blot analysis. RESULTS: CSDS induced anxiety-like behaviors by decreasing central activity in the open-field test and open-arm approach in the elevated plus maze test and led to social avoidance behavior in the social interaction test. CSDS mice showed upregulated NR1, NR2A, and NR2B expression in the hippocampus. KRG 20 and 40 mg/kg ameliorated anxiety-like activities and KRG 20 mg/kg alleviated social avoidance by decreasing time in the corner zone. KRG treatment recovered CSDS-induced NR1, NR2A, and NR2B protein levels in the hippocampus. CONCLUSION: These results indicate that KRG has a therapeutic effect on CSDS-induced mood disorder by alleviating N-methyl-D-aspartate receptor overexpression in the hippocampus. Elsevier 2021-03 2019-11-07 /pmc/articles/PMC8020286/ /pubmed/33841006 http://dx.doi.org/10.1016/j.jgr.2019.11.003 Text en © 2019 The Korean Society of Ginseng, Published by Elsevier Korea LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Lee, Bo-Ram
Lee, Ju-Hyun
Ko, Yong-Hyun
Seo, Jee-Yeon
Hur, Kwang-Hyun
Kim, Young-Jung
Kim, Seon-Kyung
Kim, Seong-Eon
Lee, Seok-Yong
Jang, Choon-Gon
Korean Red Ginseng reduces chronic social defeat stress-induced mood disorders via N-methyl-D-aspartate receptor modulation in mice
title Korean Red Ginseng reduces chronic social defeat stress-induced mood disorders via N-methyl-D-aspartate receptor modulation in mice
title_full Korean Red Ginseng reduces chronic social defeat stress-induced mood disorders via N-methyl-D-aspartate receptor modulation in mice
title_fullStr Korean Red Ginseng reduces chronic social defeat stress-induced mood disorders via N-methyl-D-aspartate receptor modulation in mice
title_full_unstemmed Korean Red Ginseng reduces chronic social defeat stress-induced mood disorders via N-methyl-D-aspartate receptor modulation in mice
title_short Korean Red Ginseng reduces chronic social defeat stress-induced mood disorders via N-methyl-D-aspartate receptor modulation in mice
title_sort korean red ginseng reduces chronic social defeat stress-induced mood disorders via n-methyl-d-aspartate receptor modulation in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020286/
https://www.ncbi.nlm.nih.gov/pubmed/33841006
http://dx.doi.org/10.1016/j.jgr.2019.11.003
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