Introduction: Cocoa flavonoids have been described to reduce the cardiovascular risk. Nevertheless, the involved mechanisms should be clarified and the dose-effect relation has never been evaluated. Aim: To investigate the dose-dependent effects of cocoa flavonoids on markers of endothelial and platelet activation and oxidative stress. Methods: According to a randomized, double-blind, controlled, cross-over design, 20 healthy nonsmokers were assigned to receive either five treatments with daily intake of 10 g cocoa (0, 80, 200, 500 and 800 mg cocoa flavonoids/day) in five periods lasting 1 week each. Results: Compared with flavonoid-free cocoa control, cocoa reduced sICAM-1 mean values [from 1190.2 to 1123.0; 906.3; 741.7 and 625.6 pg/mL (p = 0.0198 and p = 0.0016, for 500 and 800 mg respectively], sCD40L mean values [from 218.8 to 210.2; 165.5; 134.5 and 128.4 pg/mL (p = 0.023 and p = 0.013, for 500 and 800 mg respectively] and 8-isoprostanes F2 mean values [from 4703.9 to 4670.7; 2000.1; 2098.4 and 2052.3 pg/mL (p = 0.025; p = 0.034 and p = 0.029, for 200, 500 and 800 mg respectively)]. Conclusions: In our study we observed that short-term cocoa consumption improved proinflammatory mediators, lipid peroxidation and oxidative stress with a significant effect for higher dosages of flavonoids. Our findings suggest cocoa might be a valid tool for dietary intervention in prevention of atherosclerosis.

Cocoa consumption decreases oxidative stress, proinflammatory mediators and lipid peroxidation in healthy subjects. a randomized placebo-controlled dose-response clinical tria / Grassi, Davide; Mai, Francesca; De Feo, Martina; Barnabei, Remo; Carducci, Augusto; Desideri, Giovambattista; Necozione, Stefano; Allegaert, Leen; Bernaert, Herwig; Ferri, Claudio. - In: HIGH BLOOD PRESSURE & CARDIOVASCULAR PREVENTION. - ISSN 1179-1985. - 30:3(2023), pp. 219-225. [10.1007/s40292-023-00571-8]

Cocoa consumption decreases oxidative stress, proinflammatory mediators and lipid peroxidation in healthy subjects. a randomized placebo-controlled dose-response clinical tria

Desideri, Giovambattista;Ferri, Claudio
2023

Abstract

Introduction: Cocoa flavonoids have been described to reduce the cardiovascular risk. Nevertheless, the involved mechanisms should be clarified and the dose-effect relation has never been evaluated. Aim: To investigate the dose-dependent effects of cocoa flavonoids on markers of endothelial and platelet activation and oxidative stress. Methods: According to a randomized, double-blind, controlled, cross-over design, 20 healthy nonsmokers were assigned to receive either five treatments with daily intake of 10 g cocoa (0, 80, 200, 500 and 800 mg cocoa flavonoids/day) in five periods lasting 1 week each. Results: Compared with flavonoid-free cocoa control, cocoa reduced sICAM-1 mean values [from 1190.2 to 1123.0; 906.3; 741.7 and 625.6 pg/mL (p = 0.0198 and p = 0.0016, for 500 and 800 mg respectively], sCD40L mean values [from 218.8 to 210.2; 165.5; 134.5 and 128.4 pg/mL (p = 0.023 and p = 0.013, for 500 and 800 mg respectively] and 8-isoprostanes F2 mean values [from 4703.9 to 4670.7; 2000.1; 2098.4 and 2052.3 pg/mL (p = 0.025; p = 0.034 and p = 0.029, for 200, 500 and 800 mg respectively)]. Conclusions: In our study we observed that short-term cocoa consumption improved proinflammatory mediators, lipid peroxidation and oxidative stress with a significant effect for higher dosages of flavonoids. Our findings suggest cocoa might be a valid tool for dietary intervention in prevention of atherosclerosis.
2023
atherosclerosis; cardiovascular protection; cocoa; endothelial activation; endothelium; flavonoids; oxidative stress
01 Pubblicazione su rivista::01a Articolo in rivista
Cocoa consumption decreases oxidative stress, proinflammatory mediators and lipid peroxidation in healthy subjects. a randomized placebo-controlled dose-response clinical tria / Grassi, Davide; Mai, Francesca; De Feo, Martina; Barnabei, Remo; Carducci, Augusto; Desideri, Giovambattista; Necozione, Stefano; Allegaert, Leen; Bernaert, Herwig; Ferri, Claudio. - In: HIGH BLOOD PRESSURE & CARDIOVASCULAR PREVENTION. - ISSN 1179-1985. - 30:3(2023), pp. 219-225. [10.1007/s40292-023-00571-8]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1705424
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