Dec. 21, 2005 — Dark chocolate improves endothelial function in male smokers, according to the results of a randomized study reported in the January issue of Heart.
"The effects of chocolate on cardiovascular health are still a matter of debate," write F. Hermann, MD, from University Hospital in Zurich, Switzerland, and colleagues. "Chocolate may adversely affect cardiovascular risk because of its effects on glucose, lipids, and body weight or potentially favour cardiovascular health through antioxidative effects of chocolate ingredients, such as flavonoids (present in dark but not white chocolate)."
The objective of this study was to determine whether the beneficial antioxidant effect of polyphenol-rich dark chocolate could induce an improvement of endothelial and platelet function in healthy volunteers with known endothelial dysfunction and platelet hyperreactivity.
In this study, 25 male smokers were enrolled, and 5 chronic smokers underwent preliminary high-resolution ultrasound performed before and after ingestion of 40 g of dark chocolate and a 24-hour period of abstinence from polyphenol-rich food, such as black or green tea, onions, apples, cabbage, wine, and cocoa products. Endothelial function was reassessed by ultrasonography at 2, 4, 8, and 24 hours after chocolate ingestion.
Because of the positive results of the preliminary study, 20 subjects were randomized into 2 parallel groups. The investigators evaluated endothelial function and shear-stress–dependent platelet function at baseline, after 24 hours' abstinence from food rich in polyphenols, and 2 hours after ingestion of chocolate, either 40 g of dark chocolate or 40 g of white chocolate. Highly sensitive ultrasonography of the brachial artery was used to measure flow-mediated dilatation (FMD).
Baseline characteristics were similar in both groups, and no changes in glucose or lipids were detected 2 hours after chocolate ingestion. After 2 hours, dark chocolate improved FMD compared with baseline (7.0% ± 0.7% vs 4.4% ± 0.9%; P = .026), and this effect lasted about 8 hours. However, white chocolate had no effect on FMD.
Baseline arterial diameters were not different in the white and dark chocolate groups, and diameter did not change over time within groups. Vascular flow response did not change in either group nor was glyceryl-trinitrate–induced vasodilatation affected by either dark or white chocolate.
Two hours after dark chocolate ingestion, shear-stress–dependent platelet function decreased from 5.0% ± 0.6% to 3.2% ± 0.4% (P = .03 vs baseline), but there was no significant change after white chocolate ingestion. During the same time frame, total antioxidant status significantly increased 2 hours after ingestion of dark chocolate but not after ingestion of white chocolate (dark chocolate, 1.22 ± 0.02 vs 1.25 ± 0.02; P = .03, and white chocolate, 1.25 ± 0.04 vs 1.24 ± 0.03; not significant).
"Dark but not white chocolate induced a rapid and significant improvement of endothelial and platelet function in healthy smokers 2 - 8 hours after ingestion," the authors write. "The high flavonoid content of dark chocolate may potentially explain the mechanisms for the reduced platelet activation. Besides direct antioxidant capacities, flavonoids may influence 5-lipoxygenase activity and alter signal transduction pathways through antioxidant independent mechanisms."
The Swiss National Research Foundation funded the study. The authors have disclosed no relevant financial relationships.
Heart. 2006:92:119-120
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