Cargando…

Yuan-zhi-san inhibits tau protein aggregation in an Aβ(1–40)-induced Alzheimer's disease rat model via the ubiquitin-proteasome system

Yuan-zhi-san (YZS) is a classic type of Traditional Chinese Medicine, which has been reported to aid in the treatment of Alzheimer's disease (AD). The present study aimed to investigate the effects of YZS on tau protein aggregation, a hallmark of AD pathology, and its possible mechanisms. The r...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Bin, Xie, Pei-Jun, Hao, Yan-Wei, Guo, Yu, Yu, Jun-Rong, Gong, Dao-Yin, Guo, Jing, Zeng, Jin-Hao, Zhang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893680/
https://www.ncbi.nlm.nih.gov/pubmed/33604685
http://dx.doi.org/10.3892/mmr.2021.11918
_version_ 1783653094390759424
author Li, Bin
Xie, Pei-Jun
Hao, Yan-Wei
Guo, Yu
Yu, Jun-Rong
Gong, Dao-Yin
Guo, Jing
Zeng, Jin-Hao
Zhang, Yi
author_facet Li, Bin
Xie, Pei-Jun
Hao, Yan-Wei
Guo, Yu
Yu, Jun-Rong
Gong, Dao-Yin
Guo, Jing
Zeng, Jin-Hao
Zhang, Yi
author_sort Li, Bin
collection PubMed
description Yuan-zhi-san (YZS) is a classic type of Traditional Chinese Medicine, which has been reported to aid in the treatment of Alzheimer's disease (AD). The present study aimed to investigate the effects of YZS on tau protein aggregation, a hallmark of AD pathology, and its possible mechanisms. The results demonstrated that YZS improved learning and memory abilities, and decreased the severity of AD pathology in β-amyloid (Aβ(1–40))-induced AD rats. Moreover, YZS administration inhibited the hyperphosphorylation of tau protein at Ser199 and Thr231 sites. Several vital enzymes in the ubiquitin-proteasome system (UPS), including ubiquitin-activating enzyme E1a/b, ubiquitin-conjugating enzyme E2a, carboxyl terminus of Hsc70-interacting protein, ubiquitin C-236 terminal hydrolase L1 and 26S proteasome, were all significantly downregulated in AD rats, which indicated an impaired enzymatic cascade in the UPS. In addition, it was identified that YZS treatment partly increased the expression levels of these enzymes in the brains of AD rats. In conclusion, the present results suggested that YZS could effectively suppress the hyperphosphorylation of tau proteins, which may be partially associated with its beneficial role in restoring functionality of the UPS.
format Online
Article
Text
id pubmed-7893680
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-78936802021-03-08 Yuan-zhi-san inhibits tau protein aggregation in an Aβ(1–40)-induced Alzheimer's disease rat model via the ubiquitin-proteasome system Li, Bin Xie, Pei-Jun Hao, Yan-Wei Guo, Yu Yu, Jun-Rong Gong, Dao-Yin Guo, Jing Zeng, Jin-Hao Zhang, Yi Mol Med Rep Articles Yuan-zhi-san (YZS) is a classic type of Traditional Chinese Medicine, which has been reported to aid in the treatment of Alzheimer's disease (AD). The present study aimed to investigate the effects of YZS on tau protein aggregation, a hallmark of AD pathology, and its possible mechanisms. The results demonstrated that YZS improved learning and memory abilities, and decreased the severity of AD pathology in β-amyloid (Aβ(1–40))-induced AD rats. Moreover, YZS administration inhibited the hyperphosphorylation of tau protein at Ser199 and Thr231 sites. Several vital enzymes in the ubiquitin-proteasome system (UPS), including ubiquitin-activating enzyme E1a/b, ubiquitin-conjugating enzyme E2a, carboxyl terminus of Hsc70-interacting protein, ubiquitin C-236 terminal hydrolase L1 and 26S proteasome, were all significantly downregulated in AD rats, which indicated an impaired enzymatic cascade in the UPS. In addition, it was identified that YZS treatment partly increased the expression levels of these enzymes in the brains of AD rats. In conclusion, the present results suggested that YZS could effectively suppress the hyperphosphorylation of tau proteins, which may be partially associated with its beneficial role in restoring functionality of the UPS. D.A. Spandidos 2021-04 2021-02-15 /pmc/articles/PMC7893680/ /pubmed/33604685 http://dx.doi.org/10.3892/mmr.2021.11918 Text en Copyright: © Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Li, Bin
Xie, Pei-Jun
Hao, Yan-Wei
Guo, Yu
Yu, Jun-Rong
Gong, Dao-Yin
Guo, Jing
Zeng, Jin-Hao
Zhang, Yi
Yuan-zhi-san inhibits tau protein aggregation in an Aβ(1–40)-induced Alzheimer's disease rat model via the ubiquitin-proteasome system
title Yuan-zhi-san inhibits tau protein aggregation in an Aβ(1–40)-induced Alzheimer's disease rat model via the ubiquitin-proteasome system
title_full Yuan-zhi-san inhibits tau protein aggregation in an Aβ(1–40)-induced Alzheimer's disease rat model via the ubiquitin-proteasome system
title_fullStr Yuan-zhi-san inhibits tau protein aggregation in an Aβ(1–40)-induced Alzheimer's disease rat model via the ubiquitin-proteasome system
title_full_unstemmed Yuan-zhi-san inhibits tau protein aggregation in an Aβ(1–40)-induced Alzheimer's disease rat model via the ubiquitin-proteasome system
title_short Yuan-zhi-san inhibits tau protein aggregation in an Aβ(1–40)-induced Alzheimer's disease rat model via the ubiquitin-proteasome system
title_sort yuan-zhi-san inhibits tau protein aggregation in an aβ(1–40)-induced alzheimer's disease rat model via the ubiquitin-proteasome system
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893680/
https://www.ncbi.nlm.nih.gov/pubmed/33604685
http://dx.doi.org/10.3892/mmr.2021.11918
work_keys_str_mv AT libin yuanzhisaninhibitstauproteinaggregationinanab140inducedalzheimersdiseaseratmodelviatheubiquitinproteasomesystem
AT xiepeijun yuanzhisaninhibitstauproteinaggregationinanab140inducedalzheimersdiseaseratmodelviatheubiquitinproteasomesystem
AT haoyanwei yuanzhisaninhibitstauproteinaggregationinanab140inducedalzheimersdiseaseratmodelviatheubiquitinproteasomesystem
AT guoyu yuanzhisaninhibitstauproteinaggregationinanab140inducedalzheimersdiseaseratmodelviatheubiquitinproteasomesystem
AT yujunrong yuanzhisaninhibitstauproteinaggregationinanab140inducedalzheimersdiseaseratmodelviatheubiquitinproteasomesystem
AT gongdaoyin yuanzhisaninhibitstauproteinaggregationinanab140inducedalzheimersdiseaseratmodelviatheubiquitinproteasomesystem
AT guojing yuanzhisaninhibitstauproteinaggregationinanab140inducedalzheimersdiseaseratmodelviatheubiquitinproteasomesystem
AT zengjinhao yuanzhisaninhibitstauproteinaggregationinanab140inducedalzheimersdiseaseratmodelviatheubiquitinproteasomesystem
AT zhangyi yuanzhisaninhibitstauproteinaggregationinanab140inducedalzheimersdiseaseratmodelviatheubiquitinproteasomesystem