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The impact of ginsenosides on cognitive deficits in experimental animal studies of Alzheimer’s disease: a systematic review
BACKGROUND: The efficacy of ginsenoside treatment on cognitive decline in individuals with Alzheimer’s disease (AD) has yet to be investigated. In this protocal, we conducted a systematic review to evaluate the effect of ginsenosides on cognitive deficits in experimental rodent AD models. METHODS: W...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619356/ https://www.ncbi.nlm.nih.gov/pubmed/26497388 http://dx.doi.org/10.1186/s12906-015-0894-y |
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author | Sheng, Chenxia Peng, Weijun Xia, Zi-an Wang, Yang Chen, Zeqi Su, Nanxiang Wang, Zhe |
author_facet | Sheng, Chenxia Peng, Weijun Xia, Zi-an Wang, Yang Chen, Zeqi Su, Nanxiang Wang, Zhe |
author_sort | Sheng, Chenxia |
collection | PubMed |
description | BACKGROUND: The efficacy of ginsenoside treatment on cognitive decline in individuals with Alzheimer’s disease (AD) has yet to be investigated. In this protocal, we conducted a systematic review to evaluate the effect of ginsenosides on cognitive deficits in experimental rodent AD models. METHODS: We identified eligible studies by searching seven electronic databases spanning from January 1980 to October 2014. We assessed the study quality, evaluated the efficacy of ginsenoside treatment, and performed a stratified meta-analysis and meta-regression analysis to assess the influence of the study design on ginsenoside efficacy. RESULTS: Twelve studies fulfilled our inclusion criteria from a total of 283 publications. The overall methodological quality of these studies was poor. The meta-analysis revealed that ginsenosides have a statistically significant positive effect on cognitive performance in experimental AD models. The stratified analysis revealed that ginsenoside Rg1 had the greatest effect on acquisition and retention memory in AD models. The effect size was significantly higher for both acquisition and retention memory in studies that used female animals compared with male animals. CONCLUSIONS: We conclude that ginsenosides might reduce cognitive deficits in AD models. However, additional well-designed and well-reported animal studies are needed to inform further clinical investigations. |
format | Online Article Text |
id | pubmed-4619356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46193562015-10-26 The impact of ginsenosides on cognitive deficits in experimental animal studies of Alzheimer’s disease: a systematic review Sheng, Chenxia Peng, Weijun Xia, Zi-an Wang, Yang Chen, Zeqi Su, Nanxiang Wang, Zhe BMC Complement Altern Med Research Article BACKGROUND: The efficacy of ginsenoside treatment on cognitive decline in individuals with Alzheimer’s disease (AD) has yet to be investigated. In this protocal, we conducted a systematic review to evaluate the effect of ginsenosides on cognitive deficits in experimental rodent AD models. METHODS: We identified eligible studies by searching seven electronic databases spanning from January 1980 to October 2014. We assessed the study quality, evaluated the efficacy of ginsenoside treatment, and performed a stratified meta-analysis and meta-regression analysis to assess the influence of the study design on ginsenoside efficacy. RESULTS: Twelve studies fulfilled our inclusion criteria from a total of 283 publications. The overall methodological quality of these studies was poor. The meta-analysis revealed that ginsenosides have a statistically significant positive effect on cognitive performance in experimental AD models. The stratified analysis revealed that ginsenoside Rg1 had the greatest effect on acquisition and retention memory in AD models. The effect size was significantly higher for both acquisition and retention memory in studies that used female animals compared with male animals. CONCLUSIONS: We conclude that ginsenosides might reduce cognitive deficits in AD models. However, additional well-designed and well-reported animal studies are needed to inform further clinical investigations. BioMed Central 2015-10-24 /pmc/articles/PMC4619356/ /pubmed/26497388 http://dx.doi.org/10.1186/s12906-015-0894-y Text en © Sheng et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Sheng, Chenxia Peng, Weijun Xia, Zi-an Wang, Yang Chen, Zeqi Su, Nanxiang Wang, Zhe The impact of ginsenosides on cognitive deficits in experimental animal studies of Alzheimer’s disease: a systematic review |
title | The impact of ginsenosides on cognitive deficits in experimental animal studies of Alzheimer’s disease: a systematic review |
title_full | The impact of ginsenosides on cognitive deficits in experimental animal studies of Alzheimer’s disease: a systematic review |
title_fullStr | The impact of ginsenosides on cognitive deficits in experimental animal studies of Alzheimer’s disease: a systematic review |
title_full_unstemmed | The impact of ginsenosides on cognitive deficits in experimental animal studies of Alzheimer’s disease: a systematic review |
title_short | The impact of ginsenosides on cognitive deficits in experimental animal studies of Alzheimer’s disease: a systematic review |
title_sort | impact of ginsenosides on cognitive deficits in experimental animal studies of alzheimer’s disease: a systematic review |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619356/ https://www.ncbi.nlm.nih.gov/pubmed/26497388 http://dx.doi.org/10.1186/s12906-015-0894-y |
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