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Study on the neuroprotective effects of Genistein on Alzheimer’s disease

Along with the aging of the world population, the incidence rate of Alzheimer's disease (AD) has been increasing. At present, AD has become one of the most serious problems faced by modern medicine. Studies have shown that estrogen has a positive effect on AD, but estrogen has the side effect o...

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Detalles Bibliográficos
Autores principales: Duan, Xiaoying, Li, Yanshuang, Xu, Fei, Ding, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119804/
https://www.ncbi.nlm.nih.gov/pubmed/33704934
http://dx.doi.org/10.1002/brb3.2100
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author Duan, Xiaoying
Li, Yanshuang
Xu, Fei
Ding, Hong
author_facet Duan, Xiaoying
Li, Yanshuang
Xu, Fei
Ding, Hong
author_sort Duan, Xiaoying
collection PubMed
description Along with the aging of the world population, the incidence rate of Alzheimer's disease (AD) has been increasing. At present, AD has become one of the most serious problems faced by modern medicine. Studies have shown that estrogen has a positive effect on AD, but estrogen has the side effect of leading to tumors. Recent in vivo studies have shown that genistein, one of the selective estrogen receptor modulators (SERMs), can improve brain function through the blood–brain barrier (BBB), antagonize the toxicity of amyloid β‐protein (Aβ), that is, to inhibit neurotoxicity due to aggregation of beta amyloid protein, and have neuroprotective effects. In addition, the use of Gen can avoid the risk of endometrial cancer and breast cancer caused by estrogen therapy while exerting an estrogen‐like effect, which has some potential for the delay and treatment of AD.
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spelling pubmed-81198042021-05-20 Study on the neuroprotective effects of Genistein on Alzheimer’s disease Duan, Xiaoying Li, Yanshuang Xu, Fei Ding, Hong Brain Behav Reviews Along with the aging of the world population, the incidence rate of Alzheimer's disease (AD) has been increasing. At present, AD has become one of the most serious problems faced by modern medicine. Studies have shown that estrogen has a positive effect on AD, but estrogen has the side effect of leading to tumors. Recent in vivo studies have shown that genistein, one of the selective estrogen receptor modulators (SERMs), can improve brain function through the blood–brain barrier (BBB), antagonize the toxicity of amyloid β‐protein (Aβ), that is, to inhibit neurotoxicity due to aggregation of beta amyloid protein, and have neuroprotective effects. In addition, the use of Gen can avoid the risk of endometrial cancer and breast cancer caused by estrogen therapy while exerting an estrogen‐like effect, which has some potential for the delay and treatment of AD. John Wiley and Sons Inc. 2021-03-11 /pmc/articles/PMC8119804/ /pubmed/33704934 http://dx.doi.org/10.1002/brb3.2100 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Duan, Xiaoying
Li, Yanshuang
Xu, Fei
Ding, Hong
Study on the neuroprotective effects of Genistein on Alzheimer’s disease
title Study on the neuroprotective effects of Genistein on Alzheimer’s disease
title_full Study on the neuroprotective effects of Genistein on Alzheimer’s disease
title_fullStr Study on the neuroprotective effects of Genistein on Alzheimer’s disease
title_full_unstemmed Study on the neuroprotective effects of Genistein on Alzheimer’s disease
title_short Study on the neuroprotective effects of Genistein on Alzheimer’s disease
title_sort study on the neuroprotective effects of genistein on alzheimer’s disease
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119804/
https://www.ncbi.nlm.nih.gov/pubmed/33704934
http://dx.doi.org/10.1002/brb3.2100
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