Glucose-Dependent Insulinotropic Polypeptide Inhibits AGE-Induced NADPH Oxidase-Derived Oxidative Stress Generation and Foam Cell Formation in Macrophages Partly via AMPK Activation.
Humans
Foam Cells
/ metabolism
Glycation End Products, Advanced
/ metabolism
Oxidative Stress
/ drug effects
NADPH Oxidases
/ metabolism
AMP-Activated Protein Kinases
/ metabolism
Reactive Oxygen Species
/ metabolism
Cyclin-Dependent Kinase 5
/ metabolism
Gastric Inhibitory Polypeptide
/ metabolism
CD36 Antigens
/ metabolism
U937 Cells
Macrophages
/ metabolism
Lipoproteins, LDL
AGEs
AMPK
CD36
Cdk5
GIP
NADPH oxidase
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
08 Sep 2024
08 Sep 2024
Historique:
received:
03
08
2024
revised:
02
09
2024
accepted:
06
09
2024
medline:
14
9
2024
pubmed:
14
9
2024
entrez:
14
9
2024
Statut:
epublish
Résumé
Glucose-dependent insulinotropic polypeptide (GIP) of the incretin group has been shown to exert pleiotropic actions. There is growing evidence that advanced glycation end products (AGEs), senescent macromolecules formed at an accelerated rate under chronic hyperglycemic conditions, play a role in the pathogenesis of atherosclerotic cardiovascular disease in diabetes. However, whether and how GIP could inhibit the AGE-induced foam cell formation of macrophages, an initial step of atherosclerosis remains to be elucidated. In this study, we address these issues. We found that AGEs increased oxidized low-density-lipoprotein uptake into reactive oxygen species (ROS) generation and
Identifiants
pubmed: 39273671
pii: ijms25179724
doi: 10.3390/ijms25179724
pii:
doi:
Substances chimiques
Glycation End Products, Advanced
0
NADPH Oxidases
EC 1.6.3.-
AMP-Activated Protein Kinases
EC 2.7.11.31
Reactive Oxygen Species
0
Cyclin-Dependent Kinase 5
EC 2.7.11.1
Gastric Inhibitory Polypeptide
59392-49-3
CD36 Antigens
0
CDK5 protein, human
EC 2.7.11.22
oxidized low density lipoprotein
0
Lipoproteins, LDL
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Japan Association for Diabetes Education and Care
ID : 2021-YNG-002
Organisme : Japan Society for the Promotion of Science
ID : 20K07075
Organisme : Japan Society for the Promotion of Science
ID : 24K09316
Organisme : Research Grant Award 2022 from the Japanese Society of Anti-Aging Medicine
ID : 2022-2