Abstract
Carotenoids are effective antioxidants in vitro, but they are also susceptible to autoxidation, which generates volatile and biologically active aldehydes and ketones. In a previous study, we showed that autoxidized β-carotene inhibits Na+-K+-ATPase activity more effectively than aldehydic products derived from lipid peroxidation, such as 4-hydroxynonenal. In this study, we compared mitochondrial dysfunction in cultured human K562 erythroleukaemic and 28 SV4 retinal pigment epithelium (RPE) cells in response to the degradation products of β-carotene autoxidation using the MTT assay. We found that oxidized β-carotene is cytotoxic and that mitochondrial function is decreased in both K562 and RPE cells. In addition, the RPE cells were more resistant to this form of oxidative stress, suggesting that its cytotoxicity may depend on cellular antioxidant capacity.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 239-243 |
| Number of pages | 5 |
| Journal | Experimental Eye Research |
| Volume | 81 |
| Issue number | 2 |
| DOIs | |
| State | Published - Aug 2005 |
Keywords
- β-carotene
- Carotenoid derived aldehydes
- K562 cells
- Oxidative stress
- Retinal pigment epithelial cells
ASJC Scopus subject areas
- Ophthalmology
- Sensory Systems
- Cellular and Molecular Neuroscience
Fingerprint
Dive into the research topics of 'Toxicity of oxidized β-carotene to cultured human cells'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS