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Curcumin Modulates DNA Methyltransferase Functions in a Cellular Model of Diabetic Retinopathy
A. Maugeri, MG. Mazzone, F. Giuliano, M. Vinciguerra, G. Basile, M. Barchitta, A. Agodi,
Language English Country United States
Document type Journal Article
NLK
Free Medical Journals
from 2008
PubMed Central
from 2008
Europe PubMed Central
from 2008
ProQuest Central
from 2014-01-01
Open Access Digital Library
from 2008-01-01
Open Access Digital Library
from 2008-01-01
Open Access Digital Library
from 2009-01-01
Medline Complete (EBSCOhost)
from 2011-01-01
Health & Medicine (ProQuest)
from 2014-01-01
Wiley-Blackwell Open Access Titles
from 2008
PubMed
30057682
DOI
10.1155/2018/5407482
Knihovny.cz E-resources
- MeSH
- Cell Line MeSH
- DNA-Cytosine Methylases metabolism MeSH
- Diabetic Retinopathy drug therapy metabolism MeSH
- Diabetes Mellitus, Experimental drug therapy metabolism MeSH
- Curcumin pharmacology therapeutic use MeSH
- Humans MeSH
- Oxidative Stress drug effects MeSH
- Reactive Oxygen Species metabolism MeSH
- Cell Survival drug effects MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
Hyperglycaemia-induced oxidative stress appears to be involved in the aetiology of diabetic retinopathy (DR), a major public health issue, via altering DNA methylation process. We investigated the effect of hyperglycaemia on retinal DNA methyltransferase (DNMT) expression in diabetic mice, using Gene Expression Omnibus datasets. We also evaluated the effect of curcumin both on high glucose-induced reactive oxygen species (ROS) production and altered DNMT functions, in a cellular model of DR. We observed that three months of hyperglycaemia, in insulin-deficient Ins2 Akita mice, decrease DNMT1 and DNMT3a expression levels. In retinal pigment epithelium (RPE) cells, we also demonstrated that high glucose-induced ROS production precedes upregulation of DNMT expression and activity, suggesting that changes in DNMT function could be mediated by oxidative stress via a potential dual effect. The early effect results in decreased DNMT activity, accompanied by the highest ROS production, while long-term oxidative stress increases DNMT activity and DNMT1 expression. Interestingly, treatment with 25 μM curcumin for 6 hours restores ROS production, as well as DNMT functions, altered by the exposure of RPE to acute and chronic high glucose concentration. Our study suggests that curcumin may represent an effective antioxidant compound against DR, via restoring oxidative stress and DNMT functions, though further studies are recommended.
International Clinical Research Center St Anne's University Hospital Brno Czech Republic
Research and Development Department SIFI SpA Via Ercole Patti 36 Catania 95025 Italy
References provided by Crossref.org
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