Muniyappa Ranganath, Hall Gail, Kolodziej Terrie L, Karne Rajaram J, Crandon Sonja K, Quon Michael J
Diabetes Unit, National Center for Complementary and Alternative Medicine, National Institutes of Health, Bethesda, MD, USA.
Am J Clin Nutr. 2008 Dec;88(6):1685-96. doi: 10.3945/ajcn.2008.26457.
Essential hypertension is characterized by reciprocal relations between endothelial dysfunction and insulin resistance. Cocoa flavanols stimulate production of the vasodilator nitric oxide from vascular endothelium.
The objective was to test the hypothesis that consumption of cocoa may simultaneously lower blood pressure, improve endothelial dysfunction, and ameliorate insulin resistance in subjects with essential hypertension.
We conducted a randomized, placebo-controlled, double-blind, crossover trial of a flavanol-rich cocoa drink (150 mL twice a day, approximately 900 mg flavanols/d) in individuals with essential hypertension (n = 20). Antihypertensive medications were discontinued before study enrollment. After a 7-d cocoa-free run-in period, cocoa or flavanol-poor placebo (approximately 28 mg flavanols/d) treatment for 2 wk was followed by a 1-wk washout and then crossover to the other treatment arm. Blood pressure was measured thrice weekly. At baseline and after each treatment period, we assessed insulin sensitivity (hyperinsulinemic-isoglycemic glucose clamp) and insulin-stimulated changes in brachial artery diameter and forearm skeletal muscle capillary recruitment (Doppler ultrasound with or without microbubble contrast).
Cocoa treatment for 2 wk increased insulin-stimulated changes in brachial artery diameter when compared with placebo [median percentage increase from baseline (25th-75th percentile): 8.3 (4.2-11.3) compared with 5.9 (-0.3 to 9.6); P < 0.04]. Nevertheless, cocoa treatment did not significantly reduce blood pressure or improve insulin resistance and had no significant effects on skeletal muscle capillary recruitment, circulating plasma concentrations of adipocytokines, or endothelial adhesion molecules.
Daily consumption of flavanol-rich cocoa for 2 wk is not sufficient to reduce blood pressure or improve insulin resistance in human subjects with essential hypertension. This trial was registered at clinicaltrials.gov as NCT00099476.
原发性高血压的特征是内皮功能障碍与胰岛素抵抗之间存在相互关系。可可黄烷醇可刺激血管内皮产生血管舒张剂一氧化氮。
检验食用可可可能同时降低原发性高血压患者血压、改善内皮功能障碍并减轻胰岛素抵抗这一假设。
我们对20例原发性高血压患者进行了一项随机、安慰剂对照、双盲、交叉试验,给予富含黄烷醇的可可饮料(每天2次,每次150 mL,约900 mg黄烷醇/天)。在研究入组前停用抗高血压药物。经过7天无可可的导入期后,给予可可或低黄烷醇安慰剂(约28 mg黄烷醇/天)治疗2周,随后进行1周的洗脱期,然后交叉至另一治疗组。每周测量3次血压。在基线期和每个治疗期后,我们评估胰岛素敏感性(高胰岛素-正常血糖葡萄糖钳夹法)以及胰岛素刺激的肱动脉直径变化和前臂骨骼肌毛细血管募集情况(使用或不使用微泡造影剂的多普勒超声)。
与安慰剂相比,可可治疗2周可增加胰岛素刺激的肱动脉直径变化[相对于基线的中位数百分比增加(第25 - 75百分位数):8.3(4.2 - 11.3),而安慰剂组为5.9(-0.3至9.6);P < 0.04]。然而,可可治疗并未显著降低血压或改善胰岛素抵抗,对骨骼肌毛细血管募集、循环血浆中脂肪细胞因子浓度或内皮黏附分子也无显著影响。
在原发性高血压患者中,每日食用富含黄烷醇的可可2周不足以降低血压或改善胰岛素抵抗。该试验已在clinicaltrials.gov上注册,注册号为NCT00099476。