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Repeated Administration of Korea Red Ginseng Extract Increases Non-Rapid Eye Movement Sleep via GABA(A)ergic Systems

The current inquiry was conducted to assess the change in sleep architecture after long periods of administration to determine whether ginseng can be used in the therapy of sleeplessness. Following post-surgical recovery, red ginseng extract (RGE, 200 mg/ kg) was orally administrated to rats for 9 d...

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Autores principales: Lee, Chung-Il, Kim, Chung-Soo, Han, Jin-Yi, Oh, Eun-Hye, Oh, Ki-Wan, Eun, Jae Soon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Ginseng 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659601/
https://www.ncbi.nlm.nih.gov/pubmed/23717143
http://dx.doi.org/10.5142/jgr.2012.36.4.403
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author Lee, Chung-Il
Kim, Chung-Soo
Han, Jin-Yi
Oh, Eun-Hye
Oh, Ki-Wan
Eun, Jae Soon
author_facet Lee, Chung-Il
Kim, Chung-Soo
Han, Jin-Yi
Oh, Eun-Hye
Oh, Ki-Wan
Eun, Jae Soon
author_sort Lee, Chung-Il
collection PubMed
description The current inquiry was conducted to assess the change in sleep architecture after long periods of administration to determine whether ginseng can be used in the therapy of sleeplessness. Following post-surgical recovery, red ginseng extract (RGE, 200 mg/ kg) was orally administrated to rats for 9 d. Data were gathered on the 1st, 5th, and 9th day, and an electroencephalogram was recorded 24 h after RGE administration. Polygraphic signs of unobstructed sleep-wake activities were simultaneously recorded with sleep-wake recording electrodes from 11:00 a.m. to 5:00 p.m. for 6 h. Rodents were generally tamed to freely moving polygraphic recording conditions. Although the 1st and 5th day of RGE treatment showed no effect on power densities in non-rapid eye movement (NREM) and rapid eye movement (REM) sleep, the 9th day of RGE administration showed augmented α-wave (8.0 to 13.0 Hz) power densities in NREM and REM sleep. RGE increased total sleep and NREM sleep. The total percentage of wakefulness was only decreased on the 9th day, and the number of sleep-wake cycles was reduced after the repeated administration of RGE. Thus, the repeated administration of RGE increased NREM sleep in rats. The α-wave activities in the cortical electroencephalograms were increased in sleep architecture by RGE. Moreover, the levels of both α- and β-subunits of the γ-aminobutyric acid (GABA)(A) receptor were reduced in the hypothalamus of the RGE-treated groups. The level of glutamic acid decarboxylase was over-expressed in the hypothalamus. These results demonstrate that RGE increases NREM sleep via GABA(A)ergic systems.
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spelling pubmed-36596012013-05-28 Repeated Administration of Korea Red Ginseng Extract Increases Non-Rapid Eye Movement Sleep via GABA(A)ergic Systems Lee, Chung-Il Kim, Chung-Soo Han, Jin-Yi Oh, Eun-Hye Oh, Ki-Wan Eun, Jae Soon J Ginseng Res Articles The current inquiry was conducted to assess the change in sleep architecture after long periods of administration to determine whether ginseng can be used in the therapy of sleeplessness. Following post-surgical recovery, red ginseng extract (RGE, 200 mg/ kg) was orally administrated to rats for 9 d. Data were gathered on the 1st, 5th, and 9th day, and an electroencephalogram was recorded 24 h after RGE administration. Polygraphic signs of unobstructed sleep-wake activities were simultaneously recorded with sleep-wake recording electrodes from 11:00 a.m. to 5:00 p.m. for 6 h. Rodents were generally tamed to freely moving polygraphic recording conditions. Although the 1st and 5th day of RGE treatment showed no effect on power densities in non-rapid eye movement (NREM) and rapid eye movement (REM) sleep, the 9th day of RGE administration showed augmented α-wave (8.0 to 13.0 Hz) power densities in NREM and REM sleep. RGE increased total sleep and NREM sleep. The total percentage of wakefulness was only decreased on the 9th day, and the number of sleep-wake cycles was reduced after the repeated administration of RGE. Thus, the repeated administration of RGE increased NREM sleep in rats. The α-wave activities in the cortical electroencephalograms were increased in sleep architecture by RGE. Moreover, the levels of both α- and β-subunits of the γ-aminobutyric acid (GABA)(A) receptor were reduced in the hypothalamus of the RGE-treated groups. The level of glutamic acid decarboxylase was over-expressed in the hypothalamus. These results demonstrate that RGE increases NREM sleep via GABA(A)ergic systems. The Korean Society of Ginseng 2012-10 /pmc/articles/PMC3659601/ /pubmed/23717143 http://dx.doi.org/10.5142/jgr.2012.36.4.403 Text en Copyright ©2012, The Korean Society of Ginseng http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Lee, Chung-Il
Kim, Chung-Soo
Han, Jin-Yi
Oh, Eun-Hye
Oh, Ki-Wan
Eun, Jae Soon
Repeated Administration of Korea Red Ginseng Extract Increases Non-Rapid Eye Movement Sleep via GABA(A)ergic Systems
title Repeated Administration of Korea Red Ginseng Extract Increases Non-Rapid Eye Movement Sleep via GABA(A)ergic Systems
title_full Repeated Administration of Korea Red Ginseng Extract Increases Non-Rapid Eye Movement Sleep via GABA(A)ergic Systems
title_fullStr Repeated Administration of Korea Red Ginseng Extract Increases Non-Rapid Eye Movement Sleep via GABA(A)ergic Systems
title_full_unstemmed Repeated Administration of Korea Red Ginseng Extract Increases Non-Rapid Eye Movement Sleep via GABA(A)ergic Systems
title_short Repeated Administration of Korea Red Ginseng Extract Increases Non-Rapid Eye Movement Sleep via GABA(A)ergic Systems
title_sort repeated administration of korea red ginseng extract increases non-rapid eye movement sleep via gaba(a)ergic systems
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659601/
https://www.ncbi.nlm.nih.gov/pubmed/23717143
http://dx.doi.org/10.5142/jgr.2012.36.4.403
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