Trans ε viniferin decreases amyloid deposits and inflammation in a mouse transgenic Alzheimer model.
As Alzheimer's disease (AD) induces several cellular and molecular damages, it could be interesting to use multi-target molecules for therapeutics. We previously published that trans ε-viniferin induced the disaggregation of Aβ42 peptide and inhibited the inflammatory response in primary cellul...
Main Authors: | , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2019-01-01
|
Series: | PLoS ONE |
Online Access: | https://doi.org/10.1371/journal.pone.0212663 |
id |
doaj-6104f88045bb463db21808ccbf871d92 |
---|---|
record_format |
Article |
spelling |
doaj-6104f88045bb463db21808ccbf871d922021-03-03T20:52:22ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01142e021266310.1371/journal.pone.0212663Trans ε viniferin decreases amyloid deposits and inflammation in a mouse transgenic Alzheimer model.Martial CaillaudJérôme GuillardDamien RichardSerge MilinDamien ChassaingMarc PaccalinGuylène PageAgnès Rioux BilanAs Alzheimer's disease (AD) induces several cellular and molecular damages, it could be interesting to use multi-target molecules for therapeutics. We previously published that trans ε-viniferin induced the disaggregation of Aβ42 peptide and inhibited the inflammatory response in primary cellular model of AD. Here, effects of this stilbenoid were evaluated in transgenic APPswePS1dE9 mice. We report that trans ε-viniferin could go through the blood brain barrier, reduces size and density of amyloid deposits and decreases reactivity of astrocytes and microglia, after a weekly intraperitoneal injection at 10 mg/kg from 3 to 6 months of age.https://doi.org/10.1371/journal.pone.0212663 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Martial Caillaud Jérôme Guillard Damien Richard Serge Milin Damien Chassaing Marc Paccalin Guylène Page Agnès Rioux Bilan |
spellingShingle |
Martial Caillaud Jérôme Guillard Damien Richard Serge Milin Damien Chassaing Marc Paccalin Guylène Page Agnès Rioux Bilan Trans ε viniferin decreases amyloid deposits and inflammation in a mouse transgenic Alzheimer model. PLoS ONE |
author_facet |
Martial Caillaud Jérôme Guillard Damien Richard Serge Milin Damien Chassaing Marc Paccalin Guylène Page Agnès Rioux Bilan |
author_sort |
Martial Caillaud |
title |
Trans ε viniferin decreases amyloid deposits and inflammation in a mouse transgenic Alzheimer model. |
title_short |
Trans ε viniferin decreases amyloid deposits and inflammation in a mouse transgenic Alzheimer model. |
title_full |
Trans ε viniferin decreases amyloid deposits and inflammation in a mouse transgenic Alzheimer model. |
title_fullStr |
Trans ε viniferin decreases amyloid deposits and inflammation in a mouse transgenic Alzheimer model. |
title_full_unstemmed |
Trans ε viniferin decreases amyloid deposits and inflammation in a mouse transgenic Alzheimer model. |
title_sort |
trans ε viniferin decreases amyloid deposits and inflammation in a mouse transgenic alzheimer model. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2019-01-01 |
description |
As Alzheimer's disease (AD) induces several cellular and molecular damages, it could be interesting to use multi-target molecules for therapeutics. We previously published that trans ε-viniferin induced the disaggregation of Aβ42 peptide and inhibited the inflammatory response in primary cellular model of AD. Here, effects of this stilbenoid were evaluated in transgenic APPswePS1dE9 mice. We report that trans ε-viniferin could go through the blood brain barrier, reduces size and density of amyloid deposits and decreases reactivity of astrocytes and microglia, after a weekly intraperitoneal injection at 10 mg/kg from 3 to 6 months of age. |
url |
https://doi.org/10.1371/journal.pone.0212663 |
work_keys_str_mv |
AT martialcaillaud transeviniferindecreasesamyloiddepositsandinflammationinamousetransgenicalzheimermodel AT jeromeguillard transeviniferindecreasesamyloiddepositsandinflammationinamousetransgenicalzheimermodel AT damienrichard transeviniferindecreasesamyloiddepositsandinflammationinamousetransgenicalzheimermodel AT sergemilin transeviniferindecreasesamyloiddepositsandinflammationinamousetransgenicalzheimermodel AT damienchassaing transeviniferindecreasesamyloiddepositsandinflammationinamousetransgenicalzheimermodel AT marcpaccalin transeviniferindecreasesamyloiddepositsandinflammationinamousetransgenicalzheimermodel AT guylenepage transeviniferindecreasesamyloiddepositsandinflammationinamousetransgenicalzheimermodel AT agnesriouxbilan transeviniferindecreasesamyloiddepositsandinflammationinamousetransgenicalzheimermodel |
_version_ |
1714820008084766720 |