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Rg3-enriched ginseng extract ameliorates scopolamine-induced learning deficits in mice
BACKGROUND: Ginseng (Panax ginseng C.A. Meyer) has been used as a traditional herb in the treatment of many medical disorders. Ginsenosides, which are triterpene derivatives that contain sugar moieties, are the main pharmacological ingredients in ginseng. This study was designed to investigate the e...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758096/ https://www.ncbi.nlm.nih.gov/pubmed/26887326 http://dx.doi.org/10.1186/s12906-016-1050-z |
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author | Kim, Jiyoung Shim, Jaesung Lee, Siyoung Cho, Woo-Hyun Hong, Eunyoung Lee, Jin Hee Han, Jung-Soo Lee, Hyong Joo Lee, Ki Won |
author_facet | Kim, Jiyoung Shim, Jaesung Lee, Siyoung Cho, Woo-Hyun Hong, Eunyoung Lee, Jin Hee Han, Jung-Soo Lee, Hyong Joo Lee, Ki Won |
author_sort | Kim, Jiyoung |
collection | PubMed |
description | BACKGROUND: Ginseng (Panax ginseng C.A. Meyer) has been used as a traditional herb in the treatment of many medical disorders. Ginsenosides, which are triterpene derivatives that contain sugar moieties, are the main pharmacological ingredients in ginseng. This study was designed to investigate the effect of ginsenoside Rg3-enriched ginseng extract (Rg3GE) on scopolamine-induced memory impairment in mice. METHODS: Rg3GE (50 and 100 mg/kg) were administered to C57BL/6 mice by oral gavage for 14 days (days 1–14). Memory impairment was induced by scopolamine (1 mg/kg, intraperitoneal injection) for 6 days (days 914). The Morris water maze test was used to assess hippocampus-dependent spatial memory. The effects of scopolamine with or without Rg3GE on acetylcholinesterase and nuclear factor-κB (NF-κB) in the hippocampus were also examined. RESULTS: Mice with scopolamine treatment alone showed impairments in the acquisition and retention of spatial memory. Mice that received Rg3GE and scopolamine showed no scopolamine-induced impairment in the acquisition of spatial memory. Oral administration of Rg3GE suppressed the scopolamine-mediated increase in acetylcholinesterase activity and stimulation of the NF-κB pathway (i.e., phosphorylation of p65) in the hippocampus. CONCLUSION: These findings suggest that Rg3GE may stabilize scopolamine-induced memory deficits through the inhibition of acetylcholinesterase activity and NF-κB signaling in the hippocampus. |
format | Online Article Text |
id | pubmed-4758096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47580962016-02-19 Rg3-enriched ginseng extract ameliorates scopolamine-induced learning deficits in mice Kim, Jiyoung Shim, Jaesung Lee, Siyoung Cho, Woo-Hyun Hong, Eunyoung Lee, Jin Hee Han, Jung-Soo Lee, Hyong Joo Lee, Ki Won BMC Complement Altern Med Research Article BACKGROUND: Ginseng (Panax ginseng C.A. Meyer) has been used as a traditional herb in the treatment of many medical disorders. Ginsenosides, which are triterpene derivatives that contain sugar moieties, are the main pharmacological ingredients in ginseng. This study was designed to investigate the effect of ginsenoside Rg3-enriched ginseng extract (Rg3GE) on scopolamine-induced memory impairment in mice. METHODS: Rg3GE (50 and 100 mg/kg) were administered to C57BL/6 mice by oral gavage for 14 days (days 1–14). Memory impairment was induced by scopolamine (1 mg/kg, intraperitoneal injection) for 6 days (days 914). The Morris water maze test was used to assess hippocampus-dependent spatial memory. The effects of scopolamine with or without Rg3GE on acetylcholinesterase and nuclear factor-κB (NF-κB) in the hippocampus were also examined. RESULTS: Mice with scopolamine treatment alone showed impairments in the acquisition and retention of spatial memory. Mice that received Rg3GE and scopolamine showed no scopolamine-induced impairment in the acquisition of spatial memory. Oral administration of Rg3GE suppressed the scopolamine-mediated increase in acetylcholinesterase activity and stimulation of the NF-κB pathway (i.e., phosphorylation of p65) in the hippocampus. CONCLUSION: These findings suggest that Rg3GE may stabilize scopolamine-induced memory deficits through the inhibition of acetylcholinesterase activity and NF-κB signaling in the hippocampus. BioMed Central 2016-02-18 /pmc/articles/PMC4758096/ /pubmed/26887326 http://dx.doi.org/10.1186/s12906-016-1050-z Text en © Kim et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kim, Jiyoung Shim, Jaesung Lee, Siyoung Cho, Woo-Hyun Hong, Eunyoung Lee, Jin Hee Han, Jung-Soo Lee, Hyong Joo Lee, Ki Won Rg3-enriched ginseng extract ameliorates scopolamine-induced learning deficits in mice |
title | Rg3-enriched ginseng extract ameliorates scopolamine-induced learning deficits in mice |
title_full | Rg3-enriched ginseng extract ameliorates scopolamine-induced learning deficits in mice |
title_fullStr | Rg3-enriched ginseng extract ameliorates scopolamine-induced learning deficits in mice |
title_full_unstemmed | Rg3-enriched ginseng extract ameliorates scopolamine-induced learning deficits in mice |
title_short | Rg3-enriched ginseng extract ameliorates scopolamine-induced learning deficits in mice |
title_sort | rg3-enriched ginseng extract ameliorates scopolamine-induced learning deficits in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4758096/ https://www.ncbi.nlm.nih.gov/pubmed/26887326 http://dx.doi.org/10.1186/s12906-016-1050-z |
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