التفاصيل البيبلوغرافية
| العنوان: |
Resveratrol reduces amyloid-beta (Aβ)-induced paralysis through targeting proteostasis in an Alzheimer model of Caenorhabditis elegans. |
| المؤلفون: |
Regitz, Charlotte, Fitzenberger, Elena, Mahn, Friederike, Dußling, Lisa, Wenzel, Uwe |
| المصدر: |
European Journal of Nutrition; Mar2016, Vol. 55 Issue 2, p741-747, 7p, 4 Graphs |
| مصطلحات موضوعية: |
PROTEIN metabolism, PARALYSIS, AUTOPHAGY, ANALYSIS of variance, BIOLOGICAL models, LYSOSOMES, MITOCHONDRIA, NEMATODES, POLYMERASE chain reaction, PROBABILITY theory, STATISTICS, T-test (Statistics), DATA analysis, RESVERATROL, DATA analysis software, DESCRIPTIVE statistics, IN vivo studies, PREVENTION |
| مصطلحات جغرافية: |
GERMANY |
| مستخلص: |
Purpose: Resveratrol is a polyphenol present in red wine for which the capability of directly interfering with the hallmark of Alzheimer's disease (AD), i.e. toxic β-amyloid protein (Aβ) aggregation, has been shown recently. Since the stimulation of proteostasis could explain reduced Aβ-aggregation, we searched for proteostasis targets of resveratrol. Methods: The transgenic Caenorhabditis elegans strain CL2006, expressing Aβ under control of a muscle-specific promoter and responding to Aβ-toxicity with paralysis, was used as a model. Target identification was accomplished through specific knockdowns of proteostasis genes by RNA interference. Effects of resveratrol on protein aggregation were identified using ProteoStat Detection Reagent, and activation of proteasomal degradation by resveratrol was finally proven using a specific fluorogenic peptide substrate. Results: Resveratrol at a concentration of 100 µM caused a 40 % decrease in paralysis. UBL-5 involved in unfolded protein response (UPR) in mitochondria proved to be necessary for the prevention of Aβ-toxicity by resveratrol. Also XBP-1, which represents an endoplasmic reticulum-resident factor involved in UPR, was identified to be necessary for the effects of resveratrol. Regarding protein degradation pathways, the inhibition of macroautophagy and chaperone-mediated autophagy prevented resveratrol from reducing paralysis as did the inhibition of proteasomal degradation. Finally, resveratrol reduced the amount of lysosomes, suggesting increased flux of proteins through the autophagy pathways and activated proteasomal degradation. Conclusions: Resveratrol reduces the Aβ-induced toxicity in a C. elegans model of AD by targeting specific proteins involved in proteostasis and thereby reduces the amount of aggregated Aβ. [ABSTRACT FROM AUTHOR] |
|
Copyright of European Journal of Nutrition is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) |
| قاعدة البيانات: |
Complementary Index |
