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Korean Red Ginseng inhibits methamphetamine addictive behaviors by regulating dopaminergic and NMDAergic system in rodents

BACKGROUND: Methamphetamine (METH) is the most widely used psychostimulant and has been known to exhibit reinforcing effects even after long abstinence. We showed the inhibitory effect of Korean Red Ginseng extract (RGE) on METH-induced addictive behaviors in animal models mimicking the human drug-u...

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Autores principales: Lee, Bo-Ram, Sung, Su-Jeong, Hur, Kwang-Hyun, Kim, Seong-Eon, Ma, Shi-Xun, Kim, Seon-Kyung, Ko, Yong-Hyun, Kim, Young-Jung, Lee, Youyoung, Lee, Seok-Yong, Jang, Choon-Gon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753524/
https://www.ncbi.nlm.nih.gov/pubmed/35058731
http://dx.doi.org/10.1016/j.jgr.2021.05.007
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author Lee, Bo-Ram
Sung, Su-Jeong
Hur, Kwang-Hyun
Kim, Seong-Eon
Ma, Shi-Xun
Kim, Seon-Kyung
Ko, Yong-Hyun
Kim, Young-Jung
Lee, Youyoung
Lee, Seok-Yong
Jang, Choon-Gon
author_facet Lee, Bo-Ram
Sung, Su-Jeong
Hur, Kwang-Hyun
Kim, Seong-Eon
Ma, Shi-Xun
Kim, Seon-Kyung
Ko, Yong-Hyun
Kim, Young-Jung
Lee, Youyoung
Lee, Seok-Yong
Jang, Choon-Gon
author_sort Lee, Bo-Ram
collection PubMed
description BACKGROUND: Methamphetamine (METH) is the most widely used psychostimulant and has been known to exhibit reinforcing effects even after long abstinence. We showed the inhibitory effect of Korean Red Ginseng extract (RGE) on METH-induced addictive behaviors in animal models mimicking the human drug-use pattern. METHODS: We first investigated the effect of RGE on the acquisition of METH-induced dependence using self-administration and conditioned place preference (CPP) tests. Additionally, further experiments such as METH-induced motivational behavior and seeking behavior were conducted. To study the underlying mechanism, dopamine receptor, dopamine transporter, and N-methyl-D-aspartate receptor were assessed through Western blot analysis. RESULTS: Treatment with RGE significantly reduced METH-induced self-administration on a fixed-ratio 1 schedule of reinforcement. It could be also decreased a progressive ratio schedule, and inhibited METH-primed reinstatement. In CPP, RGE significantly prevented the development of METH-induced CPP. Moreover, RGE not only shortened the withdrawal period clearly, but also prevented the reinstatement of CPP. RGE treatment also reversed METH-induced overexpression of dopamine transporter, dopamine receptor D1, and NMDA receptor in the nucleus accumbens. CONCLUSION: Our findings reflect that RGE has therapeutic potential to suppress METH-induced addictive behaviors by regulating dopaminergic and NMDAergic system.
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spelling pubmed-87535242022-01-19 Korean Red Ginseng inhibits methamphetamine addictive behaviors by regulating dopaminergic and NMDAergic system in rodents Lee, Bo-Ram Sung, Su-Jeong Hur, Kwang-Hyun Kim, Seong-Eon Ma, Shi-Xun Kim, Seon-Kyung Ko, Yong-Hyun Kim, Young-Jung Lee, Youyoung Lee, Seok-Yong Jang, Choon-Gon J Ginseng Res Research Article BACKGROUND: Methamphetamine (METH) is the most widely used psychostimulant and has been known to exhibit reinforcing effects even after long abstinence. We showed the inhibitory effect of Korean Red Ginseng extract (RGE) on METH-induced addictive behaviors in animal models mimicking the human drug-use pattern. METHODS: We first investigated the effect of RGE on the acquisition of METH-induced dependence using self-administration and conditioned place preference (CPP) tests. Additionally, further experiments such as METH-induced motivational behavior and seeking behavior were conducted. To study the underlying mechanism, dopamine receptor, dopamine transporter, and N-methyl-D-aspartate receptor were assessed through Western blot analysis. RESULTS: Treatment with RGE significantly reduced METH-induced self-administration on a fixed-ratio 1 schedule of reinforcement. It could be also decreased a progressive ratio schedule, and inhibited METH-primed reinstatement. In CPP, RGE significantly prevented the development of METH-induced CPP. Moreover, RGE not only shortened the withdrawal period clearly, but also prevented the reinstatement of CPP. RGE treatment also reversed METH-induced overexpression of dopamine transporter, dopamine receptor D1, and NMDA receptor in the nucleus accumbens. CONCLUSION: Our findings reflect that RGE has therapeutic potential to suppress METH-induced addictive behaviors by regulating dopaminergic and NMDAergic system. Elsevier 2022-01 2021-05-20 /pmc/articles/PMC8753524/ /pubmed/35058731 http://dx.doi.org/10.1016/j.jgr.2021.05.007 Text en © 2021 The Korean Society of Ginseng. Publishing services by Elsevier B.V. https://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
Sung, Su-Jeong
Hur, Kwang-Hyun
Kim, Seong-Eon
Ma, Shi-Xun
Kim, Seon-Kyung
Ko, Yong-Hyun
Kim, Young-Jung
Lee, Youyoung
Lee, Seok-Yong
Jang, Choon-Gon
Korean Red Ginseng inhibits methamphetamine addictive behaviors by regulating dopaminergic and NMDAergic system in rodents
title Korean Red Ginseng inhibits methamphetamine addictive behaviors by regulating dopaminergic and NMDAergic system in rodents
title_full Korean Red Ginseng inhibits methamphetamine addictive behaviors by regulating dopaminergic and NMDAergic system in rodents
title_fullStr Korean Red Ginseng inhibits methamphetamine addictive behaviors by regulating dopaminergic and NMDAergic system in rodents
title_full_unstemmed Korean Red Ginseng inhibits methamphetamine addictive behaviors by regulating dopaminergic and NMDAergic system in rodents
title_short Korean Red Ginseng inhibits methamphetamine addictive behaviors by regulating dopaminergic and NMDAergic system in rodents
title_sort korean red ginseng inhibits methamphetamine addictive behaviors by regulating dopaminergic and nmdaergic system in rodents
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753524/
https://www.ncbi.nlm.nih.gov/pubmed/35058731
http://dx.doi.org/10.1016/j.jgr.2021.05.007
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