Red Ginseng Extract Attenuates Kainate-Induced Excitotoxicity by Antioxidative Effects
This study investigated the neuroprotective activity of red ginseng extract (RGE, Panax ginseng, C. A. Meyer) against kainic acid- (KA-) induced excitotoxicity in vitro and in vivo. In hippocampal cells, RGE inhibited KA-induced excitotoxicity in a dose-dependent manner as measured by the MTT assay....
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Hindawi Publishing Corporation
2012
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485976/ |
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pubmed-34859762012-11-06 Red Ginseng Extract Attenuates Kainate-Induced Excitotoxicity by Antioxidative Effects Han, Jin-Yi Ahn, Sun-Young Oh, Eun-Hye Nam, Sang-Yoon Hong, Jin Tae Oh, Ki-Wan Lee, Mi Kyeong Research Article This study investigated the neuroprotective activity of red ginseng extract (RGE, Panax ginseng, C. A. Meyer) against kainic acid- (KA-) induced excitotoxicity in vitro and in vivo. In hippocampal cells, RGE inhibited KA-induced excitotoxicity in a dose-dependent manner as measured by the MTT assay. To study the possible mechanisms of the RGE-mediated neuroprotective effect against KA-induced cytotoxicity, we examined the levels of intracellular reactive oxygen species (ROS) and [Ca2+]i in cultured hippocampal neurons and found that RGE treatment dose-dependently inhibited intracellular ROS and [Ca2+]i elevation. Oral administration of RGE (30 and 200 mg/kg) in mice decreased the malondialdehyde (MDA) level induced by KA injection (30 mg/kg, i.p.). In addition, similar results were obtained after pretreatment with the radical scavengers Trolox and N, N′-dimethylthiourea (DMTU). Finally, after confirming the protective effect of RGE on hippocampal brain-derived neurotropic factor (BDNF) protein levels, we found that RGE is active compounds mixture in KA-induced hippocampal mossy-fiber function improvement. Furthermore, RGE eliminated 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals, and the IC50 was approximately 10 mg/ml. The reductive activity of RGE, as measured by reaction with hydroxyl radical (•OH), was similar to trolox. The second-order rate constant of RGE for •OH was 3.5–4.5 × 109 M−1·S−1. Therefore, these results indicate that RGE possesses radical reduction activity and alleviates KA-induced excitotoxicity by quenching ROS in hippocampal neurons. Hindawi Publishing Corporation 2012 2012-10-23 /pmc/articles/PMC3485976/ /pubmed/23133495 http://dx.doi.org/10.1155/2012/479016 Text en Copyright © 2012 Jin-Yi Han et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Han, Jin-Yi Ahn, Sun-Young Oh, Eun-Hye Nam, Sang-Yoon Hong, Jin Tae Oh, Ki-Wan Lee, Mi Kyeong |
spellingShingle |
Han, Jin-Yi Ahn, Sun-Young Oh, Eun-Hye Nam, Sang-Yoon Hong, Jin Tae Oh, Ki-Wan Lee, Mi Kyeong Red Ginseng Extract Attenuates Kainate-Induced Excitotoxicity by Antioxidative Effects |
author_facet |
Han, Jin-Yi Ahn, Sun-Young Oh, Eun-Hye Nam, Sang-Yoon Hong, Jin Tae Oh, Ki-Wan Lee, Mi Kyeong |
author_sort |
Han, Jin-Yi |
title |
Red Ginseng Extract Attenuates Kainate-Induced Excitotoxicity by Antioxidative Effects |
title_short |
Red Ginseng Extract Attenuates Kainate-Induced Excitotoxicity by Antioxidative Effects |
title_full |
Red Ginseng Extract Attenuates Kainate-Induced Excitotoxicity by Antioxidative Effects |
title_fullStr |
Red Ginseng Extract Attenuates Kainate-Induced Excitotoxicity by Antioxidative Effects |
title_full_unstemmed |
Red Ginseng Extract Attenuates Kainate-Induced Excitotoxicity by Antioxidative Effects |
title_sort |
red ginseng extract attenuates kainate-induced excitotoxicity by antioxidative effects |
description |
This study investigated the neuroprotective activity of red ginseng extract (RGE, Panax ginseng, C. A. Meyer) against kainic acid- (KA-) induced excitotoxicity in vitro and in vivo. In hippocampal cells, RGE inhibited KA-induced excitotoxicity in a dose-dependent manner as measured by the MTT assay. To study the possible mechanisms of the RGE-mediated neuroprotective effect against KA-induced cytotoxicity, we examined the levels of intracellular reactive oxygen species (ROS) and [Ca2+]i in cultured hippocampal neurons and found that RGE treatment dose-dependently inhibited intracellular ROS and [Ca2+]i
elevation. Oral administration of RGE (30 and 200 mg/kg) in mice decreased the malondialdehyde (MDA) level induced by KA injection (30 mg/kg, i.p.). In addition, similar results were obtained after pretreatment with the radical scavengers Trolox and N, N′-dimethylthiourea (DMTU). Finally, after confirming the protective effect of RGE on hippocampal brain-derived neurotropic factor (BDNF) protein levels, we found that RGE is active compounds mixture in KA-induced hippocampal mossy-fiber function improvement. Furthermore, RGE eliminated 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals, and the IC50 was approximately 10 mg/ml. The reductive activity of RGE, as measured by reaction with hydroxyl radical (•OH), was similar to trolox. The second-order rate constant of RGE for •OH was 3.5–4.5 × 109 M−1·S−1. Therefore, these results indicate that RGE possesses radical reduction activity and alleviates KA-induced excitotoxicity by quenching ROS in hippocampal neurons. |
publisher |
Hindawi Publishing Corporation |
publishDate |
2012 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485976/ |
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1611920568766955520 |