Cargando…

LongShengZhi Capsule Attenuates Alzheimer-Like Pathology in APP/PS1 Double Transgenic Mice by Reducing Neuronal Oxidative Stress and Inflammation

Alzheimer’s disease (AD) is the most common form of dementia in the elderly. It may be caused by oxidative stress, inflammation, and cerebrovascular dysfunctions in the brain. LongShengZhi Capsule (LSZ), a traditional Chinese medicine, has been approved by the China Food and Drug Administration for...

Descripción completa

Detalles Bibliográficos
Autores principales: Yin, Zequn, Wang, Xuerui, Zheng, Shihong, Cao, Peichang, Chen, Yuanli, Yu, Maoyun, Liao, Chenzhong, Zhang, Zhongyuan, Han, Jihong, Duan, Yajun, Yang, Xiaoxiao, Zhang, Shuang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719723/
https://www.ncbi.nlm.nih.gov/pubmed/33328962
http://dx.doi.org/10.3389/fnagi.2020.582455
_version_ 1783619734836609024
author Yin, Zequn
Wang, Xuerui
Zheng, Shihong
Cao, Peichang
Chen, Yuanli
Yu, Maoyun
Liao, Chenzhong
Zhang, Zhongyuan
Han, Jihong
Duan, Yajun
Yang, Xiaoxiao
Zhang, Shuang
author_facet Yin, Zequn
Wang, Xuerui
Zheng, Shihong
Cao, Peichang
Chen, Yuanli
Yu, Maoyun
Liao, Chenzhong
Zhang, Zhongyuan
Han, Jihong
Duan, Yajun
Yang, Xiaoxiao
Zhang, Shuang
author_sort Yin, Zequn
collection PubMed
description Alzheimer’s disease (AD) is the most common form of dementia in the elderly. It may be caused by oxidative stress, inflammation, and cerebrovascular dysfunctions in the brain. LongShengZhi Capsule (LSZ), a traditional Chinese medicine, has been approved by the China Food and Drug Administration for treatment of patients with cardiovascular/cerebrovascular disease. LSZ contains several neuroprotective ingredients, including Hirudo, Astmgali Radix, Carthami Flos (Honghua), Persicae Semen (Taoren), Acori Tatarinowii Rhizoma (Shichangpu), and Acanthopanax Senticosus (Ciwujia). In this study, we aimed to determine the effect of LSZ on the AD process. Double transgenic mice expressing the amyloid-β precursor protein and mutant human presenilin 1 (APP/PS1) to model AD were treated with LSZ for 7 months starting at 2 months of age. LSZ significantly improved the cognition of the mice without adverse effects, indicating its high degree of safety and efficacy after a long-term treatment. LSZ reduced AD biomarker Aβ plaque accumulation by inhibiting β-secretase and γ-secretase gene expression. LSZ also reduced p-Tau expression, cell death, and inflammation in the brain. Consistently, in vitro, LSZ ethanol extract enhanced neuronal viability by reducing L-glutamic acid-induced oxidative stress and inflammation in HT-22 cells. LSZ exerted antioxidative effects by enhancing superoxide dismutase and glutathione peroxidase expression, reduced Aβ accumulation by inhibiting β-secretase and γ-secretase mRNA expression, and decreased p-Tau level by inhibiting NF-κB-mediated inflammation. It also demonstrated neuroprotective effects by regulating the Fas cell surface death receptor/B-cell lymphoma 2/p53 pathway. Taken together, our study demonstrates the antioxidative stress, anti-inflammatory, and neuroprotective effects of LSZ in the AD-like pathological process and suggests it could be a potential medicine for AD treatment.
format Online
Article
Text
id pubmed-7719723
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-77197232020-12-15 LongShengZhi Capsule Attenuates Alzheimer-Like Pathology in APP/PS1 Double Transgenic Mice by Reducing Neuronal Oxidative Stress and Inflammation Yin, Zequn Wang, Xuerui Zheng, Shihong Cao, Peichang Chen, Yuanli Yu, Maoyun Liao, Chenzhong Zhang, Zhongyuan Han, Jihong Duan, Yajun Yang, Xiaoxiao Zhang, Shuang Front Aging Neurosci Neuroscience Alzheimer’s disease (AD) is the most common form of dementia in the elderly. It may be caused by oxidative stress, inflammation, and cerebrovascular dysfunctions in the brain. LongShengZhi Capsule (LSZ), a traditional Chinese medicine, has been approved by the China Food and Drug Administration for treatment of patients with cardiovascular/cerebrovascular disease. LSZ contains several neuroprotective ingredients, including Hirudo, Astmgali Radix, Carthami Flos (Honghua), Persicae Semen (Taoren), Acori Tatarinowii Rhizoma (Shichangpu), and Acanthopanax Senticosus (Ciwujia). In this study, we aimed to determine the effect of LSZ on the AD process. Double transgenic mice expressing the amyloid-β precursor protein and mutant human presenilin 1 (APP/PS1) to model AD were treated with LSZ for 7 months starting at 2 months of age. LSZ significantly improved the cognition of the mice without adverse effects, indicating its high degree of safety and efficacy after a long-term treatment. LSZ reduced AD biomarker Aβ plaque accumulation by inhibiting β-secretase and γ-secretase gene expression. LSZ also reduced p-Tau expression, cell death, and inflammation in the brain. Consistently, in vitro, LSZ ethanol extract enhanced neuronal viability by reducing L-glutamic acid-induced oxidative stress and inflammation in HT-22 cells. LSZ exerted antioxidative effects by enhancing superoxide dismutase and glutathione peroxidase expression, reduced Aβ accumulation by inhibiting β-secretase and γ-secretase mRNA expression, and decreased p-Tau level by inhibiting NF-κB-mediated inflammation. It also demonstrated neuroprotective effects by regulating the Fas cell surface death receptor/B-cell lymphoma 2/p53 pathway. Taken together, our study demonstrates the antioxidative stress, anti-inflammatory, and neuroprotective effects of LSZ in the AD-like pathological process and suggests it could be a potential medicine for AD treatment. Frontiers Media S.A. 2020-11-23 /pmc/articles/PMC7719723/ /pubmed/33328962 http://dx.doi.org/10.3389/fnagi.2020.582455 Text en Copyright © 2020 Yin, Wang, Zheng, Cao, Chen, Yu, Liao, Zhang, Han, Duan, Yang and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Yin, Zequn
Wang, Xuerui
Zheng, Shihong
Cao, Peichang
Chen, Yuanli
Yu, Maoyun
Liao, Chenzhong
Zhang, Zhongyuan
Han, Jihong
Duan, Yajun
Yang, Xiaoxiao
Zhang, Shuang
LongShengZhi Capsule Attenuates Alzheimer-Like Pathology in APP/PS1 Double Transgenic Mice by Reducing Neuronal Oxidative Stress and Inflammation
title LongShengZhi Capsule Attenuates Alzheimer-Like Pathology in APP/PS1 Double Transgenic Mice by Reducing Neuronal Oxidative Stress and Inflammation
title_full LongShengZhi Capsule Attenuates Alzheimer-Like Pathology in APP/PS1 Double Transgenic Mice by Reducing Neuronal Oxidative Stress and Inflammation
title_fullStr LongShengZhi Capsule Attenuates Alzheimer-Like Pathology in APP/PS1 Double Transgenic Mice by Reducing Neuronal Oxidative Stress and Inflammation
title_full_unstemmed LongShengZhi Capsule Attenuates Alzheimer-Like Pathology in APP/PS1 Double Transgenic Mice by Reducing Neuronal Oxidative Stress and Inflammation
title_short LongShengZhi Capsule Attenuates Alzheimer-Like Pathology in APP/PS1 Double Transgenic Mice by Reducing Neuronal Oxidative Stress and Inflammation
title_sort longshengzhi capsule attenuates alzheimer-like pathology in app/ps1 double transgenic mice by reducing neuronal oxidative stress and inflammation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719723/
https://www.ncbi.nlm.nih.gov/pubmed/33328962
http://dx.doi.org/10.3389/fnagi.2020.582455
work_keys_str_mv AT yinzequn longshengzhicapsuleattenuatesalzheimerlikepathologyinappps1doubletransgenicmicebyreducingneuronaloxidativestressandinflammation
AT wangxuerui longshengzhicapsuleattenuatesalzheimerlikepathologyinappps1doubletransgenicmicebyreducingneuronaloxidativestressandinflammation
AT zhengshihong longshengzhicapsuleattenuatesalzheimerlikepathologyinappps1doubletransgenicmicebyreducingneuronaloxidativestressandinflammation
AT caopeichang longshengzhicapsuleattenuatesalzheimerlikepathologyinappps1doubletransgenicmicebyreducingneuronaloxidativestressandinflammation
AT chenyuanli longshengzhicapsuleattenuatesalzheimerlikepathologyinappps1doubletransgenicmicebyreducingneuronaloxidativestressandinflammation
AT yumaoyun longshengzhicapsuleattenuatesalzheimerlikepathologyinappps1doubletransgenicmicebyreducingneuronaloxidativestressandinflammation
AT liaochenzhong longshengzhicapsuleattenuatesalzheimerlikepathologyinappps1doubletransgenicmicebyreducingneuronaloxidativestressandinflammation
AT zhangzhongyuan longshengzhicapsuleattenuatesalzheimerlikepathologyinappps1doubletransgenicmicebyreducingneuronaloxidativestressandinflammation
AT hanjihong longshengzhicapsuleattenuatesalzheimerlikepathologyinappps1doubletransgenicmicebyreducingneuronaloxidativestressandinflammation
AT duanyajun longshengzhicapsuleattenuatesalzheimerlikepathologyinappps1doubletransgenicmicebyreducingneuronaloxidativestressandinflammation
AT yangxiaoxiao longshengzhicapsuleattenuatesalzheimerlikepathologyinappps1doubletransgenicmicebyreducingneuronaloxidativestressandinflammation
AT zhangshuang longshengzhicapsuleattenuatesalzheimerlikepathologyinappps1doubletransgenicmicebyreducingneuronaloxidativestressandinflammation