Poly(ADP-Ribose) polymerase is activated in subjects at risk of developing type 2 diabetes and is associated with impaired vascular reactivity

Details

Serval ID
serval:BIB_D7A8E6D8DB71
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Poly(ADP-Ribose) polymerase is activated in subjects at risk of developing type 2 diabetes and is associated with impaired vascular reactivity
Journal
Circulation
Author(s)
Szabo  C., Zanchi  A., Komjati  K., Pacher  P., Krolewski  A. S., Quist  W. C., LoGerfo  F. W., Horton  E. S., Veves  A.
ISSN
1524-4539
Publication state
Published
Issued date
11/2002
Peer-reviewed
Oui
Volume
106
Number
21
Pages
2680-6
Notes
Clinical Trial
Controlled Clinical Trial
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S. --- Old month value: Nov 19
Abstract
BACKGROUND: We have previously shown that endothelial function is impaired not only in diabetes but also in subjects at risk of developing type 2 diabetes. We hypothesized that changes in the expression or activity of the endothelial isoform of nitric oxide synthase (eNOS), the receptor for advanced glycation end products (RAGE), and poly(ADP-ribose) polymerase (PARP) are related to this impairment. METHODS AND RESULTS: We included a control group of 21 healthy subjects, a group of 22 healthy individuals with parental history of type 2 diabetes, a group of 23 subjects with impaired glucose tolerance, and a group of 21 type 2 diabetic patients. Two 2-mm forearm skin biopsies were taken from each participant and used for measurements. The percentage of PARP-positive endothelial nuclei was higher in the group with parental history of type 2 diabetes and diabetic patients compared with the controls (P<0.001). Immunoreactivity for nitrotyrosine (a marker of reactive nitrogen species) was higher in the diabetic group compared with all other groups (P<0.01). No differences in the expression of eNOS and RAGE were found among all 4 groups. The polymorphism of the eNOS gene was also studied and was not found to influence eNOS expression or microvascular functional measurements. CONCLUSIONS: PARP activation is present in healthy subjects at risk of developing diabetes as well as in established type 2 diabetic patients, and it is associated with impairments in the vascular reactivity in the skin microcirculation.
Keywords
Acetylcholine Antigens, CD31/analysis/biosynthesis Biopsy Cell Nucleus/enzymology/pathology Diabetes Mellitus, Type 2/*enzymology/pathology Disease Progression Endothelium, Vascular/enzymology/pathology Enzyme Activation Female Forearm Humans Immunohistochemistry Male Microcirculation/enzymology Middle Aged Nitric Oxide Synthase/analysis/biosynthesis/genetics Nitric Oxide Synthase Type III Poly(ADP-ribose) Polymerases/analysis/*metabolism Polymorphism, Genetic Predictive Value of Tests Receptors, Immunologic/analysis/biosynthesis Reference Values Risk Assessment Skin/blood supply Statistics as Topic Tyrosine/*analogs & derivatives/analysis/biosynthesis
Pubmed
Web of science
Open Access
Yes
Create date
11/02/2008 9:30
Last modification date
20/08/2019 15:57
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