Anti-inflammatory activities of Maillard reaction products from whey protein isolate fermented by Lactobacillus gasseri 4M13 in lipopolysaccharide-stimulated RAW264.7 cells.
Animals
Anti-Inflammatory Agents
/ pharmacology
Cyclooxygenase 2
/ genetics
Extracellular Signal-Regulated MAP Kinases
/ metabolism
Fermentation
Galactose
/ metabolism
Gene Expression
/ drug effects
Glycation End Products, Advanced
JNK Mitogen-Activated Protein Kinases
/ metabolism
Lactobacillus gasseri
/ metabolism
Lipopolysaccharides
/ pharmacology
Macrophages
/ drug effects
Maillard Reaction
Mice
Nitric Oxide
/ metabolism
Phosphorylation
/ drug effects
RAW 264.7 Cells
Tumor Necrosis Factor-alpha
/ genetics
Whey Proteins
/ chemistry
Lactobacillus gasseri 4M13
Maillard reaction
anti-inflammation
galactosylation
whey protein isolate
Journal
Journal of dairy science
ISSN: 1525-3198
Titre abrégé: J Dairy Sci
Pays: United States
ID NLM: 2985126R
Informations de publication
Date de publication:
Sep 2019
Sep 2019
Historique:
received:
30
09
2018
accepted:
28
05
2019
pubmed:
22
7
2019
medline:
30
10
2019
entrez:
22
7
2019
Statut:
ppublish
Résumé
Maillard reaction products formed from whey protein isolate (WPI) and sugar have been shown to have an anti-inflammatory effect in vitro. Here, we incubated WPI and galactose (GWA) in an aqueous solution at 65°C for 24 h to produce a glycated conjugate, which was then fermented using Lactobacillus gasseri 4M13 to obtain the fermented product (F-GWA). We demonstrated that F-GWA had an anti-inflammatory effect on lipopolysaccharide (LPS)-stimulated RAW264.7 cells. It reduced both LPS-stimulated nitric oxide production and LPS-stimulated increases in the gene expression levels of tumor necrosis factor-α and cyclooxygenase-2 in a dose-dependent manner. Furthermore, F-GWA inhibited the LPS-induced phosphorylation of extracellular signal-regulated kinase and c-Jun N-terminal kinase, members of the mitogen-activated protein kinase family. The glycation process was evaluated by measuring fluorescence intensity and the furosine concentration during the Maillard reaction to form GWA. The protein modifications of WPI were analyzed using MALDI-TOF tandem mass spectrometry. We found that the combination of the Maillard reaction and L. gasseri 4M13 fermentation increased the prebiotic properties of GWA as well as organic acid production, compared with the nonreacted WPI and galactose.
Identifiants
pubmed: 31326176
pii: S0022-0302(19)30608-3
doi: 10.3168/jds.2018-15774
pii:
doi:
Substances chimiques
Anti-Inflammatory Agents
0
Glycation End Products, Advanced
0
Lipopolysaccharides
0
Tumor Necrosis Factor-alpha
0
Whey Proteins
0
Nitric Oxide
31C4KY9ESH
Cyclooxygenase 2
EC 1.14.99.1
Extracellular Signal-Regulated MAP Kinases
EC 2.7.11.24
JNK Mitogen-Activated Protein Kinases
EC 2.7.11.24
Galactose
X2RN3Q8DNE
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
7707-7716Informations de copyright
Copyright © 2019 American Dairy Science Association. Published by Elsevier Inc. All rights reserved.