Carole Vaysse

Dr. Carole Vaysse


Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2016 in Brain, Behavior, and Immunity
Verified
Journal Article
Closed access
CRC. Rey
C. Rey
ANAgnès Nadjar
Agnès Nadjar
BBB. Buaud
B. Buaud
CVCarole Vaysse
Carole Vaysse
AAA. Aubert
A. Aubert
CJCorinne Joffre
Corinne Joffre

31 March 2015 in Food & Function
Verified
Journal Article
Closed access
PDF file
LCLeslie COUEDELO
Leslie COUEDELO
SAS. Amara
S. Amara
MLManon Lecomte
Manon Lecomte
EME. Meugnier
E. Meugnier
JMJ. Monteil
J. Monteil
CVCarole Vaysse
Carole Vaysse
Formulating healthy food rich in omega 3 fatty acids requires prior knowledge of the parameters influencing their bioavailability and their metabolic fate. In this context, we studied the effects of various emulsifiers widely used in the food industry, on the gastrointestinal lipolysis of flaxseed oil emulsions in an in vitro model and on the intestinal absorption and lymphatic secretion of alpha-linolenic acid (ALA) in rats. In vitro data showed that the emulsification of flaxseed oil with soya lecithin improved the gastric lipolysis of the oil (+30%), while the presence of Tween 80 or of sodium caseinate decreased it (−80% and −40%, respectively). The in vivo data demonstrated that the intestinal absorption and the lymphatic secretion of ALA were improved with soya lecithin (Cmax = 24 mg mL−1) and reduced in the presence of sodium caseinate (Cmax = 7 mg mL−1) compared to unemulsified flaxseed oil (Cmax = 16 mg mL−1); Tween 80 had no effect. In addition, the synthesized chylomicrons were notably larger and more numerous with soya lecithin whereas they were smaller in the presence of sodium caseinate (p < 0.05). This study shows that the intestinal bioavailability of ALA was increased by the emulsification of flaxseed oil with soya lecithin via an improved lipolysis, favouring the intestinal absorption of ALA and the secretion of many large chylomicrons in lymph.

23 November 2015 in Molecular Nutrition & Food Research
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Journal Article
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PDF file
MLManon Lecomte
Manon Lecomte
LCLeslie COUEDELO
Leslie COUEDELO
EMEmmanuelle Meugnier
Emmanuelle Meugnier
PPPascale Plaisancié
Pascale Plaisancié
MLMarion Létisse
Marion Létisse
MMMarie‐Caroline Michalski
Marie‐Caroline Michalski

1 December 2012 in The Journal of Nutritional Biochemistry
Verified
Journal Article
Closed access
JSJérôme Salles
Jérôme Salles
NTnicolas tardif
nicolas tardif
Jean-Francois LandrierJean-Francois Landrier
Jean-Francois Landrier
IMISABELLE MOTHE-SATNEY
ISABELLE MOTHE-SATNEY
CGChristelle Guillet
Christelle Guillet
SWStéphane Walrand
Stéphane Walrand

1 December 2011 in Clinical Nutrition
Verified
Journal Article
Closed access
NTnicolas tardif
nicolas tardif
JSJérôme Salles
Jérôme Salles
Jean-Francois LandrierJean-Francois Landrier
Jean-Francois Landrier
IMISABELLE MOTHE-SATNEY
ISABELLE MOTHE-SATNEY
CGChristelle Guillet
Christelle Guillet
SWStéphane Walrand
Stéphane Walrand

1 September 2013 in Journal of Lipid Research
Verified
Journal Article
Open access
PDF file
CSCécilia Samieri
Cécilia Samieri
SLSimon Lorrain
Simon Lorrain
BBBenjamin Buaud
Benjamin Buaud
CVCarole Vaysse
Carole Vaysse
CBClaudine Berr
Claudine Berr
PBPascale Barberger-Gateau
Pascale Barberger-Gateau
The main risk factors for Alzheimer's disease, age and the ϵ4 allele of the APOE gene (APOE4), might modify the metabolism of n-3 PUFAs and in turn, their impact on cognition. The aim of this study was to investigate the association between dietary fat and plasma concentrations of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) in elderly persons, taking the APOE4 genotype into account. The sample was composed of 1,135 participants from the Three-City study aged 65 years and over, of whom 19% were APOE4 carriers. Mean plasma proportions of EPA [1.01%, standard deviation (SD) 0.60] and DHA (2.41%, SD 0.81) did not differ according to APOE4. In multivariate models, plasma EPA increased with frequency of fish consumption (P < 0.0001), alcohol intake (P = 0.0006), and female gender (P = 0.02), and decreased with intensive consumption of n-6 oils (P = 0.02). The positive association between fish consumption and plasma DHA was highly significant whatever the APOE genotype (P < 0.0001) but stronger in APOE4 noncarriers than in carriers (P = 0.06 for interaction). Plasma DHA increased significantly with age (P = 0.009) in APOE4 noncarriers only. These findings suggest that dietary habits, gender, and APOE4 genotype should be considered when designing interventions to increase n-3 PUFA blood levels in older people.