Related Experiment Videos
Cocoa products decrease low density lipoprotein oxidative susceptibility but do not affect biomarkers of inflammation
Surekha Mathur1, Sridevi Devaraj, Scott M Grundy
1Center for Human Nutrition, University of Texas Southwestern Medical Center, Dallas 75390-9073, USA.
The Journal of Nutrition
|December 7, 2002
Summary
Cocoa extract supplementation improved LDL oxidizability in healthy subjects. However, it did not significantly impact oxidative stress markers like urinary F(2) isoprostanes or key inflammation indicators.
Area of Science:
- Cardiovascular Health
- Nutritional Science
- Biochemistry
Background:
- Flavonoids and polyphenols possess antioxidant and anti-inflammatory properties.
- These compounds may contribute to cardiovascular disease prevention by reducing oxidative stress and inflammation.
Purpose of the Study:
- To investigate the impact of cocoa extract supplementation on oxidative stress and inflammation markers.
- To assess the effects of dark chocolate and cocoa powder on specific biomarkers in healthy individuals.
Main Methods:
- A 6-week study involving 25 healthy subjects with supplementation of dark chocolate and cocoa powder.
- Measurements included plasma flavonoid indices, LDL oxidation kinetics, urinary F(2)-isoprostanes, and inflammatory cytokines.
- Data collected at baseline, after supplementation, and after a washout period.
Main Results:
- Cocoa supplementation significantly reduced LDL (low-density lipoprotein) oxidizability, indicated by a longer lag time for conjugated diene formation.
- No significant changes were observed in plasma total phenols, oxygen radical absorbance capacity, or urinary F(2)-isoprostanes.
- Key inflammation markers, including cytokines (interleukin-1 beta, interleukin-6, tumor necrosis factor-alpha), high-sensitivity C-reactive protein, and P-selectin, remained unaffected.
Conclusions:
- Cocoa product supplementation in humans can improve LDL oxidizability.
- The supplementation did not demonstrate significant effects on urinary F(2)-isoprostanes or systemic inflammation markers in this study.