Murphy Karen J, Chronopoulos Andriana K, Singh Indu, Francis Maureen A, Moriarty Helen, Pike Marilyn J, Turner Alan H, Mann Neil J, Sinclair Andrew J
Department of Food Science, RMIT University, Melbourne, Australia.
Am J Clin Nutr. 2003 Jun;77(6):1466-73. doi: 10.1093/ajcn/77.6.1466.
Flavonoids may be partly responsible for some health benefits, including antiinflammatory action and a decreased tendency for the blood to clot. An acute dose of flavanols and oligomeric procyanidins from cocoa powder inhibits platelet activation and function over 6 h in humans.
This study sought to evaluate whether 28 d of supplementation with cocoa flavanols and related procyanidin oligomers would modulate human platelet reactivity and primary hemostasis and reduce oxidative markers in vivo.
Thirty-two healthy subjects were assigned to consume active (234 mg cocoa flavanols and procyanidins/d) or placebo (< or = 6 mg cocoa flavanols and procyanidins/d) tablets in a blinded parallel-designed study. Platelet function was determined by measuring platelet aggregation, ATP release, and expression of activation-dependent platelet antigens by using flow cytometry. Plasma was analyzed for oxidation markers and antioxidant status.
Plasma concentrations of epicatechin and catechin in the active group increased by 81% and 28%, respectively, during the intervention period. The active group had significantly lower P selectin expression and significantly lower ADP-induced aggregation and collagen-induced aggregation than did the placebo group. Plasma ascorbic acid concentrations were significantly higher in the active than in the placebo group (P < 0.05), whereas plasma oxidation markers and antioxidant status did not change in either group.
Cocoa flavanol and procyanidin supplementation for 28 d significantly increased plasma epicatechin and catechin concentrations and significantly decreased platelet function. These data support the results of acute studies that used higher doses of cocoa flavanols and procyanidins.
黄酮类化合物可能对某些健康益处负有部分责任,包括抗炎作用以及降低血液凝固的倾向。来自可可粉的急性剂量黄烷醇和原花青素低聚物在6小时内抑制人体血小板的激活和功能。
本研究旨在评估补充28天可可黄烷醇及相关原花青素低聚物是否会调节人体血小板反应性和初级止血,并降低体内氧化标志物。
在一项双盲平行设计研究中,32名健康受试者被分配服用活性片剂(234毫克可可黄烷醇和原花青素/天)或安慰剂片剂(≤6毫克可可黄烷醇和原花青素/天)。通过测量血小板聚集、ATP释放以及使用流式细胞术检测激活依赖性血小板抗原的表达来确定血小板功能。分析血浆中的氧化标志物和抗氧化状态。
在干预期间,活性组血浆中表儿茶素和儿茶素浓度分别增加了81%和28%。与安慰剂组相比,活性组P选择素表达显著降低,ADP诱导的聚集和胶原诱导的聚集也显著降低。活性组血浆抗坏血酸浓度显著高于安慰剂组(P<0.05),而两组血浆氧化标志物和抗氧化状态均未改变。
补充28天可可黄烷醇和原花青素可显著提高血浆表儿茶素和儿茶素浓度,并显著降低血小板功能。这些数据支持了使用更高剂量可可黄烷醇和原花青素的急性研究结果。