Plant- and animal- derived dietary sources of phosphatidylcholine have differential effects on immune function in the context of a high-fat diet in male Wistar rats.
egg
high-fat diet
immunology
obesity
phosphatidylcholine
soy
Journal
The Journal of nutrition
ISSN: 1541-6100
Titre abrégé: J Nutr
Pays: United States
ID NLM: 0404243
Informations de publication
Date de publication:
04 Apr 2024
04 Apr 2024
Historique:
received:
26
10
2023
revised:
20
03
2024
accepted:
02
04
2024
medline:
7
4
2024
pubmed:
7
4
2024
entrez:
6
4
2024
Statut:
aheadofprint
Résumé
Phosphatidylcholine (PC) derived from eggs has been shown to beneficially modulate T cell response and intestinal permeability under the context of a high-fat diet. The objective of this study was to determine whether there is a differential effect of plant and animal-derived sources of PC on immune function. Four-week-old male Wistar rats were randomized to consume one of 4 diets (n=10/group) for 12 weeks, all containing 1.5g of total choline/kg of diet but differing in choline forms: 1- Control Low-Fat (CLF, 20% fat, 100% free choline (FC)); 2- Control High-Fat (CHF, 50% fat, 100% FC); 3- High-Fat Egg-derived PC (EPC, 50% fat, 100% Egg-PC); 4- High-Fat Soy-derived PC (SPC, 50% fat, 100% Soy-PC). Immune cell functions and phenotypes were measured in splenocytes by ex vivo cytokine production after mitogen stimulation and flow cytometry, respectively. The SPC diet increased splenocyte IL-2 production after PMA+I stimulation compared to the CHF diet. However, the SPC group had a lower proportion of splenocytes expressing the IL-2 receptor (CD25+, p < 0.05). After PMA+I stimulation, feeding EPC normalized splenocyte production of IL-10 relative to the CLF diet while SPC did not (p < 0.05). In mesenteric lymph node lymphocytes, the SPC diet group produced more IL-2 and TNF-α after PMA+I stimulation than the CHF diet, while the EPC diet group did not. Our results suggest that both egg- and soy-derived PC may attenuate high-fat diet-induced T cell dysfunction. However, egg-PC enhances to a greater extent IL-10, a cytokine involved in promoting the resolution phase of inflammation, while soy-PC appears to elicit a greater effect on gut-associated immune responses.
Sections du résumé
BACKGROUND
BACKGROUND
Phosphatidylcholine (PC) derived from eggs has been shown to beneficially modulate T cell response and intestinal permeability under the context of a high-fat diet.
OBJECTIVES
OBJECTIVE
The objective of this study was to determine whether there is a differential effect of plant and animal-derived sources of PC on immune function.
METHODS
METHODS
Four-week-old male Wistar rats were randomized to consume one of 4 diets (n=10/group) for 12 weeks, all containing 1.5g of total choline/kg of diet but differing in choline forms: 1- Control Low-Fat (CLF, 20% fat, 100% free choline (FC)); 2- Control High-Fat (CHF, 50% fat, 100% FC); 3- High-Fat Egg-derived PC (EPC, 50% fat, 100% Egg-PC); 4- High-Fat Soy-derived PC (SPC, 50% fat, 100% Soy-PC). Immune cell functions and phenotypes were measured in splenocytes by ex vivo cytokine production after mitogen stimulation and flow cytometry, respectively.
RESULTS
RESULTS
The SPC diet increased splenocyte IL-2 production after PMA+I stimulation compared to the CHF diet. However, the SPC group had a lower proportion of splenocytes expressing the IL-2 receptor (CD25+, p < 0.05). After PMA+I stimulation, feeding EPC normalized splenocyte production of IL-10 relative to the CLF diet while SPC did not (p < 0.05). In mesenteric lymph node lymphocytes, the SPC diet group produced more IL-2 and TNF-α after PMA+I stimulation than the CHF diet, while the EPC diet group did not.
CONCLUSIONS
CONCLUSIONS
Our results suggest that both egg- and soy-derived PC may attenuate high-fat diet-induced T cell dysfunction. However, egg-PC enhances to a greater extent IL-10, a cytokine involved in promoting the resolution phase of inflammation, while soy-PC appears to elicit a greater effect on gut-associated immune responses.
Identifiants
pubmed: 38582387
pii: S0022-3166(24)00175-5
doi: 10.1016/j.tjnut.2024.04.004
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.