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Dietary intake of branched-chain amino acids in a mouse model of Alzheimer's disease: Effects on survival, behavior, and neuropathology.
Tournissac, Marine; Vandal, Milene; Tremblay, Cyntia; Bourassa, Philippe; Vancassel, Sylvie; Emond, Vincent; Gangloff, Anne; Calon, Frederic.
Afiliação
  • Tournissac M; Faculty of pharmacy, Laval University, Quebec City, QC, Canada.
  • Vandal M; Neuroscience axis, CHU de Québec-Université Laval Research Center, Quebec City, QC, Canada.
  • Tremblay C; OptiNutriBrain International Associated Laboratory (NutriNeuro France-INAF Canada).
  • Bourassa P; Institute of Nutrition and Functional Foods, Université Laval, Quebec City, QC, Canada.
  • Vancassel S; Faculty of pharmacy, Laval University, Quebec City, QC, Canada.
  • Emond V; Neuroscience axis, CHU de Québec-Université Laval Research Center, Quebec City, QC, Canada.
  • Gangloff A; OptiNutriBrain International Associated Laboratory (NutriNeuro France-INAF Canada).
  • Calon F; Institute of Nutrition and Functional Foods, Université Laval, Quebec City, QC, Canada.
Alzheimers Dement (N Y) ; 4: 677-687, 2018.
Article em En | MEDLINE | ID: mdl-30560200
ABSTRACT

INTRODUCTION:

High levels of plasmatic branched-chain amino acids (BCAA), commonly used as dietary supplements, are linked to metabolic risk factors for Alzheimer's disease (AD). BCAA directly influence amino acid transport to the brain and, therefore, neurotransmitter levels. We thus investigated the impact of BCAA on AD neuropathology in a mouse model.

METHODS:

3xTg-AD mice were fed either a control diet or a high-fat diet from 6 to 18 months of age. For the last 2 months, dietary BCAA content was adjusted to high (+50%), normal (+0%), or low (-50%).

RESULTS:

Mice fed a BCAA-supplemented high-fat diet displayed higher tau neuropathology and only four out of 13 survived. Mice on the low-BCAA diet showed higher threonine and tryptophan cortical levels while performing better on the novel object recognition task.

DISCUSSION:

These preclinical data underscore a potential risk of combining high-fat and high BCAA consumption, and possible benefits from BCAA restriction in AD.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article