Abstract |
Selenium methylselenocysteine (Se-MeSeCys) is a common selenocompound in the diet with a tested chemopreventive effect. This study investigated the potential protective effect of Se-MeSeCys against a chemical oxidative stress induced by tert-butyl hydroperoxide (t-BOOH) on human hepatoma HepG2 cells. Speciation of selenium derivatives by liquid chromatography-inductively coupled plasma mass spectrometry depicts Se-MeSeCys as the only selenocompound in the cell culture. Cell viability ( lactate dehydrogenase) and markers of oxidative status--concentration of reduced glutathione (GSH) and malondialdehyde (MDA), generation of reactive oxygen species (ROS) and activity of the antioxidant enzymes glutathione peroxidase (GPx) and glutathione reductase (GR)--were evaluated. Pretreatment of cells with Se-MeSeCys for 20 h completely prevented the enhanced cell damage, MDA concentration and GR and GPx activity and the decreased GSH induced by t-BOOH but did not prevent increased ROS generation. The results show that treatment of HepG2 cells with concentrations of Se-MeSeCys in the nanomolar to micromolar range confers a significant protection against an oxidative insult.
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Authors | Susana Cuello, Sonia Ramos, Raquel Mateos, M Angeles Martín, Yolanda Madrid, Carmen Cámara, Laura Bravo, Luis Goya |
Journal | Analytical and bioanalytical chemistry
(Anal Bioanal Chem)
Vol. 389
Issue 7-8
Pg. 2167-78
(Dec 2007)
ISSN: 1618-2650 [Electronic] Germany |
PMID | 17952420
(Publication Type: Journal Article)
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Chemical References |
- Anticarcinogenic Agents
- Organoselenium Compounds
- Reactive Oxygen Species
- Selenocysteine
- Malondialdehyde
- tert-Butylhydroperoxide
- Glutathione
- Cysteine
- selenomethylselenocysteine
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Topics |
- Anticarcinogenic Agents
(pharmacology)
- Carcinoma, Hepatocellular
(metabolism)
- Cell Line, Tumor
- Cell Survival
- Cysteine
(analogs & derivatives, pharmacology)
- Glutathione
(analysis)
- Humans
- Liver Neoplasms
(metabolism)
- Malondialdehyde
(analysis)
- Organoselenium Compounds
(pharmacology)
- Oxidative Stress
(drug effects)
- Reactive Oxygen Species
(metabolism)
- Selenocysteine
(analogs & derivatives)
- Time Factors
- tert-Butylhydroperoxide
(toxicity)
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