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Therapeutic Effect of Yi-Chi-Tsung-Ming-Tang on Amyloid β (1−40)-Induced Alzheimer's Disease-Like Phenotype via an Increase of Acetylcholine and Decrease of Amyloid β
Alzheimer's disease (AD) is an irreversible neurodegenerative disorder characterized by amyloid accumulation, neuronal death, and cognitive impairments. Yi-Chi-Tsung-Ming-Tang (YCTMT) is a traditional Chinese medicine and has never been used to enhance cognitive function and treat neurodegenera...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382387/ https://www.ncbi.nlm.nih.gov/pubmed/22754582 http://dx.doi.org/10.1155/2012/414536 |
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author | Yeh, Chung-Hsin Hsieh, Ming-Tsuen Hsueh, Chi-Mei Wu, Chi-Rei Huang, Yi-Chun Liao, Jiunn-Wang Chow, Kuan-Chih |
author_facet | Yeh, Chung-Hsin Hsieh, Ming-Tsuen Hsueh, Chi-Mei Wu, Chi-Rei Huang, Yi-Chun Liao, Jiunn-Wang Chow, Kuan-Chih |
author_sort | Yeh, Chung-Hsin |
collection | PubMed |
description | Alzheimer's disease (AD) is an irreversible neurodegenerative disorder characterized by amyloid accumulation, neuronal death, and cognitive impairments. Yi-Chi-Tsung-Ming-Tang (YCTMT) is a traditional Chinese medicine and has never been used to enhance cognitive function and treat neurodegenerative disorders such as senile dementia. Whether YCTMT has a beneficial role in improving learning and memory in AD patients remains unclear. The present study showed that oral administration of YCTMT ameliorated amyloid-β- (Aβ (1−40)) injection-induced learning and memory impairments in rats, examined using passive avoidance and Morris water-maze tests. Immunostaining and Western Blot results showed that continuous Aβ (1−40) infusion caused amyloid accumulation and decreased acetylcholine level in hippocampus. Oral administration of medium and high dose of YCTMT 7 days after the Aβ (1−40) infusion decreased amyloid accumulation area and reversed acetylcholine decline in the Aβ (1−40)-injected hippocampus, suggesting that YCTMT might inhibit Aβ plague accumulation and rescue reduced acetylcholine expression. This study has provided evidence on the beneficial role of YCTMT in ameliorating amyloid-induced AD-like symptom, indicating that YCTMT may offer an alternative strategy for treating AD. |
format | Online Article Text |
id | pubmed-3382387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33823872012-06-29 Therapeutic Effect of Yi-Chi-Tsung-Ming-Tang on Amyloid β (1−40)-Induced Alzheimer's Disease-Like Phenotype via an Increase of Acetylcholine and Decrease of Amyloid β Yeh, Chung-Hsin Hsieh, Ming-Tsuen Hsueh, Chi-Mei Wu, Chi-Rei Huang, Yi-Chun Liao, Jiunn-Wang Chow, Kuan-Chih Evid Based Complement Alternat Med Research Article Alzheimer's disease (AD) is an irreversible neurodegenerative disorder characterized by amyloid accumulation, neuronal death, and cognitive impairments. Yi-Chi-Tsung-Ming-Tang (YCTMT) is a traditional Chinese medicine and has never been used to enhance cognitive function and treat neurodegenerative disorders such as senile dementia. Whether YCTMT has a beneficial role in improving learning and memory in AD patients remains unclear. The present study showed that oral administration of YCTMT ameliorated amyloid-β- (Aβ (1−40)) injection-induced learning and memory impairments in rats, examined using passive avoidance and Morris water-maze tests. Immunostaining and Western Blot results showed that continuous Aβ (1−40) infusion caused amyloid accumulation and decreased acetylcholine level in hippocampus. Oral administration of medium and high dose of YCTMT 7 days after the Aβ (1−40) infusion decreased amyloid accumulation area and reversed acetylcholine decline in the Aβ (1−40)-injected hippocampus, suggesting that YCTMT might inhibit Aβ plague accumulation and rescue reduced acetylcholine expression. This study has provided evidence on the beneficial role of YCTMT in ameliorating amyloid-induced AD-like symptom, indicating that YCTMT may offer an alternative strategy for treating AD. Hindawi Publishing Corporation 2012 2012-06-13 /pmc/articles/PMC3382387/ /pubmed/22754582 http://dx.doi.org/10.1155/2012/414536 Text en Copyright © 2012 Chung-Hsin Yeh 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. |
spellingShingle | Research Article Yeh, Chung-Hsin Hsieh, Ming-Tsuen Hsueh, Chi-Mei Wu, Chi-Rei Huang, Yi-Chun Liao, Jiunn-Wang Chow, Kuan-Chih Therapeutic Effect of Yi-Chi-Tsung-Ming-Tang on Amyloid β (1−40)-Induced Alzheimer's Disease-Like Phenotype via an Increase of Acetylcholine and Decrease of Amyloid β |
title | Therapeutic Effect of Yi-Chi-Tsung-Ming-Tang on Amyloid β
(1−40)-Induced Alzheimer's Disease-Like Phenotype via an Increase of Acetylcholine and Decrease of Amyloid β
|
title_full | Therapeutic Effect of Yi-Chi-Tsung-Ming-Tang on Amyloid β
(1−40)-Induced Alzheimer's Disease-Like Phenotype via an Increase of Acetylcholine and Decrease of Amyloid β
|
title_fullStr | Therapeutic Effect of Yi-Chi-Tsung-Ming-Tang on Amyloid β
(1−40)-Induced Alzheimer's Disease-Like Phenotype via an Increase of Acetylcholine and Decrease of Amyloid β
|
title_full_unstemmed | Therapeutic Effect of Yi-Chi-Tsung-Ming-Tang on Amyloid β
(1−40)-Induced Alzheimer's Disease-Like Phenotype via an Increase of Acetylcholine and Decrease of Amyloid β
|
title_short | Therapeutic Effect of Yi-Chi-Tsung-Ming-Tang on Amyloid β
(1−40)-Induced Alzheimer's Disease-Like Phenotype via an Increase of Acetylcholine and Decrease of Amyloid β
|
title_sort | therapeutic effect of yi-chi-tsung-ming-tang on amyloid β
(1−40)-induced alzheimer's disease-like phenotype via an increase of acetylcholine and decrease of amyloid β |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382387/ https://www.ncbi.nlm.nih.gov/pubmed/22754582 http://dx.doi.org/10.1155/2012/414536 |
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