Imbalance in the antioxidant defence system and pro-genotoxic status induced by high glucose concentrations: In vitro testing in human liver cells.
4-Nitroquinoline-1-oxide
/ toxicity
Acetylcysteine
/ pharmacology
Antioxidants
/ pharmacology
Cell Line, Tumor
Comet Assay
DNA Damage
Glucose
Glutathione Transferase
/ metabolism
Heme Oxygenase-1
/ metabolism
Humans
Hyperglycemia
/ genetics
Liver
/ cytology
Mutagens
/ toxicity
Phospholipid Hydroperoxide Glutathione Peroxidase
/ metabolism
Reactive Oxygen Species
/ metabolism
Comet assay
Gene expression
High glucose concentration
In vitro
Liver cells
Oxidative stress response
Pro-genotoxicity
ROS
Journal
Toxicology in vitro : an international journal published in association with BIBRA
ISSN: 1879-3177
Titre abrégé: Toxicol In Vitro
Pays: England
ID NLM: 8712158
Informations de publication
Date de publication:
Dec 2020
Dec 2020
Historique:
received:
08
10
2019
revised:
18
08
2020
accepted:
12
09
2020
pubmed:
18
9
2020
medline:
10
8
2021
entrez:
17
9
2020
Statut:
ppublish
Résumé
It has been hypothesized that high glucose concentrations might contribute to the overall intracellular oxidative stress either by the direct generation of reactive oxygen species (ROS) or by altering the redox balance. Moreover, it has also been suggested that high glucose concentration can increase the susceptibility of DNA to genotoxic effects of xenobiotics. The aim of this approach was to test high glucose concentrations for pro-genotoxicity in human liver cells by setting up an in vitro model for hyperglycaemia. The experimental design included performing of tests on both human HepG2 tumour cells and HepaRG immortalized cells. Increased cell susceptibility to genotoxic xenobiotics was tested by challenging cell cultures with 4-nitroquinoline-N-oxide (4NQO) and evaluating the extent of primary DNA damage by comet assay. Moreover, we evaluated the relationship between glucose concentration and intracellular ROS, as well as the effects of glucose concentration on the induction of Nrf2-dependent genes such as Glutathione S-transferases, Heme‑oxygenase-1, and Glutathione peroxidase-4. To investigate the involvement of ROS in the induced pro-genotoxic activity, parallel experimental sets were set up by considering co-treatment of cells with the model mutagen 4NQO and the antioxidant, glutathione precursor N-acetyl-L-cysteine. High glucose concentrations caused a significant increase in the levels of primary DNA damage, with a pro-genotoxic condition closely related to the concentration of glucose in the culture medium when cells were exposed to 4NQO. High glucose concentrations also stimulated the production of ROS and down-regulated genes involved in contrasting of the effects of oxidative stress. In conclusion, in the presence of high concentrations of glucose, the cells are in unfavourable conditions for the maintenance of genome integrity.
Identifiants
pubmed: 32942007
pii: S0887-2333(20)30551-8
doi: 10.1016/j.tiv.2020.105001
pii:
doi:
Substances chimiques
Antioxidants
0
Mutagens
0
Reactive Oxygen Species
0
4-Nitroquinoline-1-oxide
56-57-5
Phospholipid Hydroperoxide Glutathione Peroxidase
EC 1.11.1.12
HMOX1 protein, human
EC 1.14.14.18
Heme Oxygenase-1
EC 1.14.14.18
Glutathione Transferase
EC 2.5.1.18
Glucose
IY9XDZ35W2
Acetylcysteine
WYQ7N0BPYC
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
105001Informations de copyright
Copyright © 2020 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.