Influence of reduced intracellular glutathione availability on the secretion of vasoactive substances by human umbilical vein endothelial cells

Citation
E. Beinder et al., Influence of reduced intracellular glutathione availability on the secretion of vasoactive substances by human umbilical vein endothelial cells, HYPERTENS P, 20(1), 2001, pp. 45-56
Citations number
23
Categorie Soggetti
Reproductive Medicine","Cardiovascular & Hematology Research
Journal title
HYPERTENSION IN PREGNANCY
ISSN journal
10641955 → ACNP
Volume
20
Issue
1
Year of publication
2001
Pages
45 - 56
Database
ISI
SICI code
1064-1955(2001)20:1<45:IORIGA>2.0.ZU;2-3
Abstract
Objective. Oxidative stress might be the reason for endothelial dysfunction in preeclampsia. The glutathione-peroxidase system is one of the primary a ntioxidants in the endothelium. We tested the effect of oxidative stress by reduction of glutathione availability on the secretion of vasoactive subst ances in endothelial cells. Methods. Endothelial cells in culture were incubated with different concent rations of buthionine-[S,R]-sulfoximine (BSO) or 1-chloro-2,4-dinitrobenzen e (CDNB), both leading to a reduced intracellular availability of glutathio ne. The secretion of the vasoactive substances nitric oxide (NO), endotheli n-1 (ET-1), and prostacyclin (PGI(2)) was measured with respect to vitality and proliferation rate of the endothelial cells in culture. Main Outcome Measure. Effect of oxidative stress on the secretion of vasoac tive substances from endothelial cells. Results. The oxidants CDNB and BSO have (in concentrations before evidence of cytotoxicity) a stimulating effect on the production of PGI(2), they inh ibit NO availability, and they do not significantly interfere with ET-1 pro duction. Conclusion. Oxidative stress in vitro induces an imbalance in the secretion of NO, ET-1, and PGI(2) in endothelial cells.