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Prolonged oral administration of Gastrodia elata extract improves spatial learning and memory of scopolamine-treated rats
Gastrodia elata (GE) is traditionally used for treatment of various disorders including neurodegenerative diseases such as Alzheimer's disease. To investigate the neuroprotective effect of GE, amyloid-β peptide (Aβ)-treated PC12 cells were cultured with GE aqueous extract. In vitro assay demons...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association for Laboratory Animal Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490148/ https://www.ncbi.nlm.nih.gov/pubmed/26155201 http://dx.doi.org/10.5625/lar.2015.31.2.69 |
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author | Park, Young-Mi Lee, Bong-Gun Park, Sang-Hoon Oh, Hong-Geun Kang, Yang-Gyu Kim, Ok-Jin Kwon, Lee-Seong Kim, Yong-Phill Choi, Min-Hyu Jeong, Yong-Seob Oh, Jisun Lee, Hak-Yong |
author_facet | Park, Young-Mi Lee, Bong-Gun Park, Sang-Hoon Oh, Hong-Geun Kang, Yang-Gyu Kim, Ok-Jin Kwon, Lee-Seong Kim, Yong-Phill Choi, Min-Hyu Jeong, Yong-Seob Oh, Jisun Lee, Hak-Yong |
author_sort | Park, Young-Mi |
collection | PubMed |
description | Gastrodia elata (GE) is traditionally used for treatment of various disorders including neurodegenerative diseases such as Alzheimer's disease. To investigate the neuroprotective effect of GE, amyloid-β peptide (Aβ)-treated PC12 cells were cultured with GE aqueous extract. In vitro assay demonstrated that 50 µM of pre-aggregated Aβ was lethal to about a half portion of PC12 cells and that Aβ aggregate-induced cell death was significantly decreased with GE treatment at ≤10 mg/mL in a dose-dependent manner. To further examine in vivo cognitive-improving effects, an artificial amnesic animal model, scopolamine-injected Sprague-Dawley rats, were orally administered the extract for 6 weeks followed by behavioral tests (the passive avoidance test and Morris water maze test). The results showed that an acute treatment with scopolamine (1 mg/kg of body weight) effectively induced memory impairment in normal rats and that the learning and memory capability of scopolamine-treated rats improved after prolonged administration of GE extract (50, 250 and 500 mg/kg of body weight for 6 weeks). These findings suggest that a GE regimen may potentially ameliorate learning and memory deficits and/or cognitive impairments caused by neuronal cell death. |
format | Online Article Text |
id | pubmed-4490148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Korean Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44901482015-07-07 Prolonged oral administration of Gastrodia elata extract improves spatial learning and memory of scopolamine-treated rats Park, Young-Mi Lee, Bong-Gun Park, Sang-Hoon Oh, Hong-Geun Kang, Yang-Gyu Kim, Ok-Jin Kwon, Lee-Seong Kim, Yong-Phill Choi, Min-Hyu Jeong, Yong-Seob Oh, Jisun Lee, Hak-Yong Lab Anim Res Original Article Gastrodia elata (GE) is traditionally used for treatment of various disorders including neurodegenerative diseases such as Alzheimer's disease. To investigate the neuroprotective effect of GE, amyloid-β peptide (Aβ)-treated PC12 cells were cultured with GE aqueous extract. In vitro assay demonstrated that 50 µM of pre-aggregated Aβ was lethal to about a half portion of PC12 cells and that Aβ aggregate-induced cell death was significantly decreased with GE treatment at ≤10 mg/mL in a dose-dependent manner. To further examine in vivo cognitive-improving effects, an artificial amnesic animal model, scopolamine-injected Sprague-Dawley rats, were orally administered the extract for 6 weeks followed by behavioral tests (the passive avoidance test and Morris water maze test). The results showed that an acute treatment with scopolamine (1 mg/kg of body weight) effectively induced memory impairment in normal rats and that the learning and memory capability of scopolamine-treated rats improved after prolonged administration of GE extract (50, 250 and 500 mg/kg of body weight for 6 weeks). These findings suggest that a GE regimen may potentially ameliorate learning and memory deficits and/or cognitive impairments caused by neuronal cell death. Korean Association for Laboratory Animal Science 2015-06 2015-06-26 /pmc/articles/PMC4490148/ /pubmed/26155201 http://dx.doi.org/10.5625/lar.2015.31.2.69 Text en Copyright © 2015 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 Park, Young-Mi Lee, Bong-Gun Park, Sang-Hoon Oh, Hong-Geun Kang, Yang-Gyu Kim, Ok-Jin Kwon, Lee-Seong Kim, Yong-Phill Choi, Min-Hyu Jeong, Yong-Seob Oh, Jisun Lee, Hak-Yong Prolonged oral administration of Gastrodia elata extract improves spatial learning and memory of scopolamine-treated rats |
title | Prolonged oral administration of Gastrodia elata extract improves spatial learning and memory of scopolamine-treated rats |
title_full | Prolonged oral administration of Gastrodia elata extract improves spatial learning and memory of scopolamine-treated rats |
title_fullStr | Prolonged oral administration of Gastrodia elata extract improves spatial learning and memory of scopolamine-treated rats |
title_full_unstemmed | Prolonged oral administration of Gastrodia elata extract improves spatial learning and memory of scopolamine-treated rats |
title_short | Prolonged oral administration of Gastrodia elata extract improves spatial learning and memory of scopolamine-treated rats |
title_sort | prolonged oral administration of gastrodia elata extract improves spatial learning and memory of scopolamine-treated rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490148/ https://www.ncbi.nlm.nih.gov/pubmed/26155201 http://dx.doi.org/10.5625/lar.2015.31.2.69 |
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