Dietary linoleic acid lowering alone does not lower arachidonic acid or endocannabinoids among women with overweight and obesity: A randomized, controlled trial.

arachidonic acid diet docosahexaenoic acid eicosapentaeonic acid endocannabinoid linoleic acid

Journal

Lipids
ISSN: 1558-9307
Titre abrégé: Lipids
Pays: United States
ID NLM: 0060450

Informations de publication

Date de publication:
Nov 2023
Historique:
revised: 23 10 2023
received: 13 09 2023
accepted: 02 11 2023
medline: 15 12 2023
pubmed: 15 12 2023
entrez: 15 12 2023
Statut: ppublish

Résumé

The linoleic acid (LA)-arachidonic acid (ARA)-inflammatory axis suggests dietary LA lowering benefits health because it lowers ARA and ARA-derived endocannabinoids (ECB). Dietary LA reduction increases concentrations of omega-3 eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) and DHA derived ECB. The aim of this study was to examine targeted reduction of dietary LA, with and without EPA and DHA, on plasma EPA and DHA and ECB (2-arachidonoyl glycerol [2-AG], anandamide [AEA], and docosahexaenoyl ethanolamide [DHA-EA]). Healthy, pre-menopausal women (n = 62, BMI 30 ± 3 kg/m

Identifiants

pubmed: 38100748
doi: 10.1002/lipd.12382
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

271-284

Subventions

Organisme : NIDDK NIH HHS
Pays : United States
Organisme : NIA NIH HHS
Pays : United States
Organisme : NIAAA NIH HHS
Pays : United States

Informations de copyright

Published 2023. This article is a U.S. Government work and is in the public domain in the USA.

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Auteurs

Amber B Courville (AB)

National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland, USA.

Sharon Majchrzak-Hong (S)

National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland, USA.

Shanna Yang (S)

National Institutes of Health, Clinical Center, Bethesda, Maryland, USA.

Sara Turner (S)

National Institutes of Health, Clinical Center, Bethesda, Maryland, USA.

Breanne Wilhite (B)

National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland, USA.

Katherine Ness Shipley (K)

National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland, USA.

Yvonne Horneffer (Y)

National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland, USA.

Anthony F Domenichiello (AF)

National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland, USA.
National Institutes of Health, National Institute of Neurological Disorders and Stroke, Bethesda, Maryland, USA.

Melanie Schwandt (M)

National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland, USA.

Roy G Cutler (RG)

National Institutes of Health, National Institute on Aging, Bethesda, Maryland, USA.

Kong Y Chen (KY)

National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland, USA.

Joseph R Hibbeln (JR)

National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland, USA.

Christopher E Ramsden (CE)

National Institutes of Health, National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland, USA.
National Institutes of Health, National Institute on Aging, Bethesda, Maryland, USA.

Classifications MeSH