Abstract
The intake of green coffee has been associated with a lower risk of diseases of oxidative etiology probably due to its high phenolic content. The present study investigated the effect of treating human HepG2 cells with different concentrations of a green coffee bean extract (GCBE) and its main hydroxycinnamic acids, 5-caffeoylquinic acid (5-CQA) and 3,5-dicaffeoylquinic acid (3,5-DCQA), and the methylxanthine caffeine (CAF), directly or prior to inducing an oxidative stress by incubating cells with 400. μM tert-butylhydroperoxide (t-BOOH). Direct treatment with GCBE (1-50. μg/mL), 5-CQA and 3,5-DCQA (1-40. μM) significantly decreased reactive oxygen species (ROS) production by HepG2 cells. Pre-treatment with GCBE, 5-CQA and 3,5-DCQA for 20. h prevented the cellular and macromolecular damage induced by t-BOOH, returning glutathione levels and the activity of antioxidant enzymes to values similar to control cells. Moreover, the increased ROS generation induced by t-BOOH was dose-dependently prevented when cells were pre-treated with GCBE, 5-CQA and 3,5-DCQA. CAF showed no protective effect. It can be concluded that GCBE and its main polyphenols, 5-CQA and 3,5-DCQA, but not caffeine, confer a significant protection against oxidative stress in vitro.
| Original language | English |
|---|---|
| Pages (from-to) | 1038-1046 |
| Number of pages | 9 |
| Journal | Food Research International |
| Volume | 62 |
| DOIs | |
| Publication status | Published - Aug 2014 |
| Externally published | Yes |
Keywords
- Caffeine
- Dietary antioxidants
- Green coffee
- Oxidative stress biomarkers
- Polyphenolic compounds
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