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Modulation of plasma N-acylethanolamine levels and physiological parameters by dietary fatty acid composition in humans.

By September 28, 2014No Comments
2014 Sep 28.

Modulation of plasma N-acylethanolamine levels and physiological parameters by dietary fatty acid composition in humans.

JLR 2014-051235R
Modulation of plasma N-acylethanolamine levels and physiological parameters by dietary fatty acid composition in humans
Peter J.H. Jones1*, Lin Lin1, Leah G. Gillingham1, Haifeng Yang1, Jaclyn M. Omar1
1 Richardson Centre for Functional Foods and Nutraceuticals, 196 Innovation Drive, University of Manitoba, Winnipeg, MB, Canada, R3T 2N2
*Corresponding author
Address: Richardson Centre for Functional Foods and Nutraceuticals, University of Manitoba, 196 Innovation Drive, Winnipeg, MB, Canada, R3T 2N2
Tel: +1 204 474 8883
Fax: +1 204 474 7552
Email address: peter.jones@umanitoba.ca (P.J.H. Jones)
Running title: Dietary fat alters circulating NAE levels in humans
Abbreviations: NAE, N-acylethanolamine; HOCO, high-oleic canola oil; FXCO, flaxseed high-oleic canola oil; WD, western diet; OEA, oleoylethanolamide; ALEA, alpha-linolenoyl ethanolamide; AEA, arachidonoyl ethanolamide, NAPE, N-acylphosphatidylethanolamine, NAPE-PLD, N-acyl phosphatidylethanolamine-specific phospholipase D; PEA, palmitoylethanolamide; CB, cannabinoid; DIO, diet-induced obesity; 2-AG, 2-arachidonoylglycerol; WAT, white adipose tissue; ALA, alpha- linoleic acid; SPE, solid-phase extraction; MRM, multiple reaction monitoring; AA, arachidonic acid; LA, linoleic acid; DHEA, docosahexaenoyl ethanolamide; LEA, linoleoyl ethanolamide; HOMA-IR, homeostatic model assessment-insulin resistance; RBC, red blood cell; OA, oleic acid
2014 Sep 28. pii: jlr.P051235. [Epub ahead of print]

Abstract

pm1N-acylethanolamines (NAE) are endogenous lipid signaling molecules involved in satiety and energetics, however, how diet impacts circulating NAE concentrations and their downstream metabolic actions in humans remains unknown. Objectives were to examine effects of diets enriched with high-oleic canola oil (HOCO) or HOCO blended with flaxseed oil (FXCO), compared to a Western diet (WD), on plasma NAE levels and the association with energy expenditure and substrate oxidation. Using a randomized controlled crossover design, 36 hypercholesterolemic participants consumed three isoenergetic diets for 28d, each containing 36% energy from fat, of which 70% was HOCO, FXCO or WD. UPLC-MS/MS was used to measure plasma NAE levels and indirect calorimetry to assess energy expenditure and substrate oxidation. After 28d, compared with WD, plasma OEA and ALEA levels were significantly increased in response to HOCO and FXCO (p = 0.002; p < 0.001), respectively. Correlation analysis demonstrated an inverse association between plasma OEA levels and percent body fat (r= -0.21, p = 0.04) and a positive association was observed between the plasma AEA/OEA ratio and android:gynoid fat (r = 0.23, p = 0.02), respectively. Results suggest that plasma NAE levels are upregulated via their dietary lipid substrates and may modulate regional and total fat mass through lipid signaling mechanisms.
Copyright © 2014, The American Society for Biochemistry and Molecular Biology.

KEYWORDS:

Arachidonoylethanolamide; Body Composition; Canola Oil; Clinical trials; Endocannabinoids; Fatty acid/Metabolism; Fatty acid/Oxidation; Oleic Acid; Oleoylethanolamide; PPARs

PMID:

 

25262934

 

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