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Protective effects of cultured and fermented ginseng extracts against scopolamine-induced memory loss in a mouse model
This study was performed to investigate the effect of a concentrate of fermented wild ginseng root culture (HLJG0701) on memory improvement in the scopolamine (SPL)-induced memory-deficient mouse model. Eight-week-old male ICR mice were used to evaluate the protective effect of HLJG0701 against the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association for Laboratory Animal Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876162/ https://www.ncbi.nlm.nih.gov/pubmed/29628975 http://dx.doi.org/10.5625/lar.2018.34.1.37 |
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author | Han, Song-Hee Kim, Sung-June Yun, Young Won Nam, Sang Yoon Lee, Hu-Jang Lee, Beom-Jun |
author_facet | Han, Song-Hee Kim, Sung-June Yun, Young Won Nam, Sang Yoon Lee, Hu-Jang Lee, Beom-Jun |
author_sort | Han, Song-Hee |
collection | PubMed |
description | This study was performed to investigate the effect of a concentrate of fermented wild ginseng root culture (HLJG0701) on memory improvement in the scopolamine (SPL)-induced memory-deficient mouse model. Eight-week-old male ICR mice were used to evaluate the protective effect of HLJG0701 against the SPL-induced memory loss animal model. The Morris water maze test, which measures hippocampus-dependent learning ability, and the Y-maze test, a short-term memory assessment test, were performed and related markers were analyzed. HLJG0701-treated groups displayed significantly reduced acetylcholinesterase activity and increased acetylcholine level compared with the SPL-administered group (SPL-G) (P<0.05). In the Y-maze test, the spontaneous alternation in al HLJG0711-treated groups was significantly increased compared with that in SPL-G (P<0.05). In the Morris water maze test, the escape latency and time spent in the target quadrant in all HLJG0701-treated groups were significantly decreased and increased, respectively, compared with those in SPL-G (P<0.05). In addition, the brain-derived neurotrophic factor level in groups treated with HLJG0701 300 and 600 mg/kg body weight was significantly increased compared with that in SPL-G (P<0.05). These results suggest that the HLJG0701 may protect against memory loss by inhibiting acetylcholinesterase activity and preventing acetylcholine deficiency. |
format | Online Article Text |
id | pubmed-5876162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Korean Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58761622018-04-06 Protective effects of cultured and fermented ginseng extracts against scopolamine-induced memory loss in a mouse model Han, Song-Hee Kim, Sung-June Yun, Young Won Nam, Sang Yoon Lee, Hu-Jang Lee, Beom-Jun Lab Anim Res Original Article This study was performed to investigate the effect of a concentrate of fermented wild ginseng root culture (HLJG0701) on memory improvement in the scopolamine (SPL)-induced memory-deficient mouse model. Eight-week-old male ICR mice were used to evaluate the protective effect of HLJG0701 against the SPL-induced memory loss animal model. The Morris water maze test, which measures hippocampus-dependent learning ability, and the Y-maze test, a short-term memory assessment test, were performed and related markers were analyzed. HLJG0701-treated groups displayed significantly reduced acetylcholinesterase activity and increased acetylcholine level compared with the SPL-administered group (SPL-G) (P<0.05). In the Y-maze test, the spontaneous alternation in al HLJG0711-treated groups was significantly increased compared with that in SPL-G (P<0.05). In the Morris water maze test, the escape latency and time spent in the target quadrant in all HLJG0701-treated groups were significantly decreased and increased, respectively, compared with those in SPL-G (P<0.05). In addition, the brain-derived neurotrophic factor level in groups treated with HLJG0701 300 and 600 mg/kg body weight was significantly increased compared with that in SPL-G (P<0.05). These results suggest that the HLJG0701 may protect against memory loss by inhibiting acetylcholinesterase activity and preventing acetylcholine deficiency. Korean Association for Laboratory Animal Science 2018-03 2018-03-22 /pmc/articles/PMC5876162/ /pubmed/29628975 http://dx.doi.org/10.5625/lar.2018.34.1.37 Text en Copyright © 2018 Korean Association for Laboratory Animal Science 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 | Original Article Han, Song-Hee Kim, Sung-June Yun, Young Won Nam, Sang Yoon Lee, Hu-Jang Lee, Beom-Jun Protective effects of cultured and fermented ginseng extracts against scopolamine-induced memory loss in a mouse model |
title | Protective effects of cultured and fermented ginseng extracts against scopolamine-induced memory loss in a mouse model |
title_full | Protective effects of cultured and fermented ginseng extracts against scopolamine-induced memory loss in a mouse model |
title_fullStr | Protective effects of cultured and fermented ginseng extracts against scopolamine-induced memory loss in a mouse model |
title_full_unstemmed | Protective effects of cultured and fermented ginseng extracts against scopolamine-induced memory loss in a mouse model |
title_short | Protective effects of cultured and fermented ginseng extracts against scopolamine-induced memory loss in a mouse model |
title_sort | protective effects of cultured and fermented ginseng extracts against scopolamine-induced memory loss in a mouse model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876162/ https://www.ncbi.nlm.nih.gov/pubmed/29628975 http://dx.doi.org/10.5625/lar.2018.34.1.37 |
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