Research Article
HUVECs from newborns with a strong family history of diabetes show diminished ROS synthesis in the presence of high glucose concentrations
Article first published online: 30 JUN 2006
DOI: 10.1002/dmrr.665
Copyright © 2005 John Wiley & Sons, Ltd.
Additional Information
How to Cite
Alvarado-Vásquez, N., Páez, A., Zapata, E., Alcázar-Leyva, S., Zenteno, E., Massó, F. and Montaño, L. F. (2007), HUVECs from newborns with a strong family history of diabetes show diminished ROS synthesis in the presence of high glucose concentrations. Diabetes Metab. Res. Rev., 23: 71–80. doi: 10.1002/dmrr.665
Publication History
- Issue published online: 28 DEC 2006
- Article first published online: 30 JUN 2006
- Manuscript Accepted: 24 MAY 2006
- Manuscript Revised: 11 MAY 2006
- Manuscript Received: 8 FEB 2006
Funded by
- Instituto Científico Pfizer-Mexico. Grant Number: SALUD-2002-COI-7630
- PAPIIT-UNAM. Grant Number: IN224906-2
- Abstract
- Article
- References
- Cited By
Keywords:
- endothelium;
- glucose;
- type 2 diabetes mellitus;
- superoxide;
- reactive oxygen species;
- oxidative stress
Abstract
Background
A family history of type 2 diabetes mellitus (DM) increases the probability to develop DM and endothelial dysfunction. The probable mechanism involves augmented reactive oxygen species (ROS) synthesis. The aim of this study was to evaluate the synthesis of ROS in human umbilical vein endothelial cells (HUVECs) obtained from healthy newborns with (experimental) and without (control) a strong family history of type 2 DM, exposed to different glucose concentrations.
Methods
HUVECs were exposed to various glucose concentrations for 24 and 48 h periods, before cell proliferation, mitochondrial activity, and mitochondrial membrane potential were determined. Intracellular ROS synthesis in the presence or absence of the mitochondrial uncoupler CCCP, cytochalasin B, or diphenyleneiodonium (DPI) was also evaluated.
Results
As opposed to control HUVECs, we found that experimental HUVECs exposed to 30 mmol/L glucose showed a 50% decrease in cell proliferation, a 90% reduction in mitochondrial activity, and a statistically significant inhibition of ROS synthesis in the presence of CCCP or cytochalasin B; DPI had no effect.
Conclusions
Our results suggest that mitochondria and NAD(P)H-oxidase from HUVECs obtained from healthy newborns with a family history of DM have an innate deficient response to high glucose concentrations. Copyright © 2006 John Wiley & Sons, Ltd.

1520-7560/asset/bannerforeground.jpg?v=1&s=97ddd213ca98f827538987e02b801875335d1a52)
1520-7560/asset/cover.gif?v=1&s=518ef24df4af0f53197d5b36e1afedd4421360a2)