Mice derived from in vitro αMEM-cultured preimplantation embryos exhibit postprandial hyperglycemia and higher inflammatory gene expression in peripheral leukocytes.
Animals
Atherosclerosis
/ diet therapy
Blastocyst
/ drug effects
Blood Glucose
/ metabolism
Calgranulin A
/ genetics
Diet
/ methods
Embryo Transfer
Embryo, Mammalian
Female
Gene Expression Regulation
Hordeum
/ chemistry
Hyperglycemia
/ diet therapy
Leukocytes
/ metabolism
Mice
NADPH Oxidase 2
/ genetics
Organic Chemicals
/ adverse effects
Oryza
/ chemistry
Postprandial Period
Pregnancy
Prenatal Exposure Delayed Effects
/ diet therapy
Tissue Culture Techniques
Tumor Necrosis Factor-alpha
/ genetics
in vitro fertilization
MEM mice
T2DM
barley
inflammation
Journal
Bioscience, biotechnology, and biochemistry
ISSN: 1347-6947
Titre abrégé: Biosci Biotechnol Biochem
Pays: England
ID NLM: 9205717
Informations de publication
Date de publication:
24 Apr 2021
24 Apr 2021
Historique:
received:
03
12
2020
accepted:
06
02
2021
pubmed:
16
2
2021
medline:
7
8
2021
entrez:
15
2
2021
Statut:
ppublish
Résumé
We examined whether peripheral leukocytes of mice derived from in vitro αMEM-cultured embryos and exhibiting type 2 diabetes had higher expression of inflammatory-related genes associated with the development of atherosclerosis. Also, we examined the impact of a barley diet on inflammatory gene expression. Adult mice were produced by embryo transfer, after culturing two-cell embryos for 48 h in either α minimal essential media (α-MEM) or potassium simplex optimized medium control media. Mice were fed either a barley or rice diet for 10 weeks. Postprandial blood glucose and mRNA levels of several inflammatory genes, including Tnfa and Nox2, in blood leukocytes were significantly higher in MEM mice fed a rice diet compared with control mice. Barley intake reduced expression of S100a8 and Nox2. In summary, MEM mice exhibited postprandial hyperglycemia and peripheral leukocytes with higher expression of genes related to the development of atherosclerosis, and barley intake reduced some gene expression.
Identifiants
pubmed: 33587104
pii: 6136288
doi: 10.1093/bbb/zbab023
doi:
Substances chimiques
Blood Glucose
0
Calgranulin A
0
Organic Chemicals
0
S100a8 protein, mouse
0
Tumor Necrosis Factor-alpha
0
alpha minimal essential medium
0
Cybb protein, mouse
EC 1.6.3.-
NADPH Oxidase 2
EC 1.6.3.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1215-1226Informations de copyright
© The Author(s) 2021. Published by Oxford University Press on behalf of Japan Society for Bioscience, Biotechnology, and Agrochemistry.