Chronic Ethanol Feeding in Mice Decreases Expression of Genes for Major Structural Bone Proteins in a Nox4-Independent Manner.
Animals
Bone Density
/ drug effects
Bone and Bones
/ drug effects
Ethanol
/ administration & dosage
Female
Gene Expression
/ drug effects
Genotype
Male
Mice
Mice, Knockout
NADPH Oxidase 4
/ genetics
NADPH Oxidases
/ genetics
Osteoblasts
/ drug effects
Oxidation-Reduction
/ drug effects
Oxidative Stress
/ drug effects
Reactive Oxygen Species
/ metabolism
Journal
The Journal of pharmacology and experimental therapeutics
ISSN: 1521-0103
Titre abrégé: J Pharmacol Exp Ther
Pays: United States
ID NLM: 0376362
Informations de publication
Date de publication:
06 2020
06 2020
Historique:
received:
03
12
2019
accepted:
23
03
2020
pubmed:
28
3
2020
medline:
12
9
2020
entrez:
28
3
2020
Statut:
ppublish
Résumé
Bone loss in response to alcohol intake has previously been hypothesized to be mediated by excessive production of reactive oxygen species via NADPH oxidase (Nox) enzymes. Nox4 is one of several Nox enzymes expressed in bone. We investigated the role of Nox4 in the chondro-osteoblastic lineage of the long bones in mice during normal chow feeding and during chronic ethanol feeding for 90 days. We generated mice with a genotype (
Identifiants
pubmed: 32213546
pii: jpet.119.264374
doi: 10.1124/jpet.119.264374
pmc: PMC7228502
doi:
Substances chimiques
Reactive Oxygen Species
0
Ethanol
3K9958V90M
NADPH Oxidase 4
EC 1.6.3.-
NADPH Oxidases
EC 1.6.3.-
Nox4 protein, mouse
EC 1.6.3.-
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
337-346Subventions
Organisme : NIAAA NIH HHS
ID : T32 AA007577
Pays : United States
Organisme : NIAAA NIH HHS
ID : R37 AA018282
Pays : United States
Organisme : NIAAA NIH HHS
ID : T35 AA021097
Pays : United States
Organisme : NIAAA NIH HHS
ID : F32 AA026480
Pays : United States
Organisme : NIAAA NIH HHS
ID : R01 AA018282
Pays : United States
Organisme : NIGMS NIH HHS
ID : R25 GM121189
Pays : United States
Informations de copyright
Copyright © 2020 by The American Society for Pharmacology and Experimental Therapeutics.
Déclaration de conflit d'intérêts
The authors declare that they have no conflicts of interest.
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