Cargando…

Ingredients in Zijuan Pu’er Tea Extract Alleviate β-Amyloid Peptide Toxicity in a Caenorhabditis elegans Model of Alzheimer’s Disease Likely through DAF-16

Amyloid-β, one of the hallmarks of Alzheimer’s disease (AD), is toxic to neurons and can also cause brain cell death. Oxidative stress is known to play an important role in AD, and there is strong evidence that oxidative stress is associated with amyloid-β. In the present study we report the protect...

Descripción completa

Detalles Bibliográficos
Autores principales: Du, Fangzhou, Zhou, Lin, Jiao, Yan, Bai, Shuju, Wang, Lu, Ma, Junfeng, Fu, Xueqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412921/
https://www.ncbi.nlm.nih.gov/pubmed/30781621
http://dx.doi.org/10.3390/molecules24040729
_version_ 1783402718325374976
author Du, Fangzhou
Zhou, Lin
Jiao, Yan
Bai, Shuju
Wang, Lu
Ma, Junfeng
Fu, Xueqi
author_facet Du, Fangzhou
Zhou, Lin
Jiao, Yan
Bai, Shuju
Wang, Lu
Ma, Junfeng
Fu, Xueqi
author_sort Du, Fangzhou
collection PubMed
description Amyloid-β, one of the hallmarks of Alzheimer’s disease (AD), is toxic to neurons and can also cause brain cell death. Oxidative stress is known to play an important role in AD, and there is strong evidence that oxidative stress is associated with amyloid-β. In the present study we report the protective effect of Zijuan Pu’er tea water extract (ZTWE) and the mixture of main ingredients (+)-catechins, caffeine and procyanidin (MCCP) in ZTWE on β-amyloid-induced toxicity in transgenic Caenorhabditis elegans (C. elegans) CL4176 expressing the human Aβ(1–42) gene. ZTWE, (+)-catechins, caffeine, procyanidin and MCCP delayed the β-amyloid-induced paralysis to different degrees. The MCCP treatment did not affect the transcript abundance of amyloid-β transgene (amy-1); however, Thioflavin T staining showed a significant decrease in Aβ accumulation compared to untreated worms. Further research using transgenic worms found that MCCP promoted the translocation of DAF-16 from cytoplasm to nucleus and increased the expression of superoxide dismutase 3 (SOD-3). In addition, MCCP decreased the reactive oxygen species (ROS) content and increased the SOD activity in CL4176 worms. In conclusion, the results suggested that MCCP had a significant protective effect on β-amyloid-induced toxicity in C. elegans by reducing β-amyloid aggregation and inducing DAF-16 nuclear translocation that could activate the downstream signal pathway and enhance resistance to oxidative stress.
format Online
Article
Text
id pubmed-6412921
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-64129212019-04-09 Ingredients in Zijuan Pu’er Tea Extract Alleviate β-Amyloid Peptide Toxicity in a Caenorhabditis elegans Model of Alzheimer’s Disease Likely through DAF-16 Du, Fangzhou Zhou, Lin Jiao, Yan Bai, Shuju Wang, Lu Ma, Junfeng Fu, Xueqi Molecules Article Amyloid-β, one of the hallmarks of Alzheimer’s disease (AD), is toxic to neurons and can also cause brain cell death. Oxidative stress is known to play an important role in AD, and there is strong evidence that oxidative stress is associated with amyloid-β. In the present study we report the protective effect of Zijuan Pu’er tea water extract (ZTWE) and the mixture of main ingredients (+)-catechins, caffeine and procyanidin (MCCP) in ZTWE on β-amyloid-induced toxicity in transgenic Caenorhabditis elegans (C. elegans) CL4176 expressing the human Aβ(1–42) gene. ZTWE, (+)-catechins, caffeine, procyanidin and MCCP delayed the β-amyloid-induced paralysis to different degrees. The MCCP treatment did not affect the transcript abundance of amyloid-β transgene (amy-1); however, Thioflavin T staining showed a significant decrease in Aβ accumulation compared to untreated worms. Further research using transgenic worms found that MCCP promoted the translocation of DAF-16 from cytoplasm to nucleus and increased the expression of superoxide dismutase 3 (SOD-3). In addition, MCCP decreased the reactive oxygen species (ROS) content and increased the SOD activity in CL4176 worms. In conclusion, the results suggested that MCCP had a significant protective effect on β-amyloid-induced toxicity in C. elegans by reducing β-amyloid aggregation and inducing DAF-16 nuclear translocation that could activate the downstream signal pathway and enhance resistance to oxidative stress. MDPI 2019-02-18 /pmc/articles/PMC6412921/ /pubmed/30781621 http://dx.doi.org/10.3390/molecules24040729 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Du, Fangzhou
Zhou, Lin
Jiao, Yan
Bai, Shuju
Wang, Lu
Ma, Junfeng
Fu, Xueqi
Ingredients in Zijuan Pu’er Tea Extract Alleviate β-Amyloid Peptide Toxicity in a Caenorhabditis elegans Model of Alzheimer’s Disease Likely through DAF-16
title Ingredients in Zijuan Pu’er Tea Extract Alleviate β-Amyloid Peptide Toxicity in a Caenorhabditis elegans Model of Alzheimer’s Disease Likely through DAF-16
title_full Ingredients in Zijuan Pu’er Tea Extract Alleviate β-Amyloid Peptide Toxicity in a Caenorhabditis elegans Model of Alzheimer’s Disease Likely through DAF-16
title_fullStr Ingredients in Zijuan Pu’er Tea Extract Alleviate β-Amyloid Peptide Toxicity in a Caenorhabditis elegans Model of Alzheimer’s Disease Likely through DAF-16
title_full_unstemmed Ingredients in Zijuan Pu’er Tea Extract Alleviate β-Amyloid Peptide Toxicity in a Caenorhabditis elegans Model of Alzheimer’s Disease Likely through DAF-16
title_short Ingredients in Zijuan Pu’er Tea Extract Alleviate β-Amyloid Peptide Toxicity in a Caenorhabditis elegans Model of Alzheimer’s Disease Likely through DAF-16
title_sort ingredients in zijuan pu’er tea extract alleviate β-amyloid peptide toxicity in a caenorhabditis elegans model of alzheimer’s disease likely through daf-16
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412921/
https://www.ncbi.nlm.nih.gov/pubmed/30781621
http://dx.doi.org/10.3390/molecules24040729
work_keys_str_mv AT dufangzhou ingredientsinzijuanpuerteaextractalleviatebamyloidpeptidetoxicityinacaenorhabditiselegansmodelofalzheimersdiseaselikelythroughdaf16
AT zhoulin ingredientsinzijuanpuerteaextractalleviatebamyloidpeptidetoxicityinacaenorhabditiselegansmodelofalzheimersdiseaselikelythroughdaf16
AT jiaoyan ingredientsinzijuanpuerteaextractalleviatebamyloidpeptidetoxicityinacaenorhabditiselegansmodelofalzheimersdiseaselikelythroughdaf16
AT baishuju ingredientsinzijuanpuerteaextractalleviatebamyloidpeptidetoxicityinacaenorhabditiselegansmodelofalzheimersdiseaselikelythroughdaf16
AT wanglu ingredientsinzijuanpuerteaextractalleviatebamyloidpeptidetoxicityinacaenorhabditiselegansmodelofalzheimersdiseaselikelythroughdaf16
AT majunfeng ingredientsinzijuanpuerteaextractalleviatebamyloidpeptidetoxicityinacaenorhabditiselegansmodelofalzheimersdiseaselikelythroughdaf16
AT fuxueqi ingredientsinzijuanpuerteaextractalleviatebamyloidpeptidetoxicityinacaenorhabditiselegansmodelofalzheimersdiseaselikelythroughdaf16