Principal component analysis of the effects of environmental enrichment and (-)-epigallocatechin-3-gallate on age-associated learning deficits in a mouse model of Down Syndrome

Down syndrome (DS) individuals present increased risk for Alzheimer's disease (AD) neuropathology and AD-type dementia. Here, we investigated the use of green tea extracts containing (-)-epigallocatechin-3-gallate (EGCG), as co-adjuvant to enhance the effects of environmental enrichment (EE) in...

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Bibliographic Details
Authors: Catuara, Silvina, Espinosa Carrasco, Jose, Erb, Ionas, Langohr, Klaus|||0000-0001-7075-9192, Notredame, Cedric, Gonzalez, Juan R., Dierssen, Mara
Format: article
Publication Date:2015
Country:España
Institution:Universitat Politècnica de Catalunya (UPC)
Repository:UPCommons. Portal del coneixement obert de la UPC
Language:English
OAI Identifier:oai:upcommons.upc.edu:2117/84867
Online Access:https://hdl.handle.net/2117/84867
https://dx.doi.org/10.3389/fnbeh.2015.00330
Access Level:Open access
Keyword:Operations research
Down syndrome
aging
(-)-epigallocatechin-3-gallate
Morris water maze
principal component analysis
MORRIS WATER MAZE
GREEN TEA POLYPHENOL
ALZHEIMERS-DISEASE
COGNITIVE DEFICITS
TRANSGENIC MICE
TS65DN MICE
NEUROPATHOLOGICAL CHANGES
CEREBRAL-CORTEX
BRAIN
PROTEIN
Investigació operativa
Classificació AMS::90 Operations research, mathematical programming::90B Operations research and management science
Àrees temàtiques de la UPC::Matemàtiques i estadística::Investigació operativa::Simulació
Description
Summary:Down syndrome (DS) individuals present increased risk for Alzheimer's disease (AD) neuropathology and AD-type dementia. Here, we investigated the use of green tea extracts containing (-)-epigallocatechin-3-gallate (EGCG), as co-adjuvant to enhance the effects of environmental enrichment (EE) in Ts65Dn mice, a segmental trisomy model of DS that partially mimics DS/AD pathology, at the age of initiation of cognitive decline. Classical repeated measures ANOVA showed that combined EE-EGCG treatment was more efficient than FE or EGCG alone to improve specific spatial learning related variables. Using principal component analysis (PCA) we found that several spatial learning parameters contributed similarly to a first PC and explained a large proportion of the variance among groups, thus representing a composite learning measure. This PC1 revealed that EGCG or FE alone had no significant effect. However, combined FE-EGCG significantly ameliorated learning alterations of middle age Ts65Dn mice. Interestingly. PCA revealed an increased variability along learning sessions with good and poor learners in Ts65Dn, and this stratification did not disappear upon treatments. Our results suggest that combining EE and EGCG represents a viable therapeutic approach for amelioration of age-related cognitive decline in DS, although its efficacy may vary across individuals.