Schram Miranda T, Stam Frank, de Jongh Renate T, de Vries Greetje, van Dijk Rob A J M, Serné Erik H, Lampe Deva, Nanayakkara Prabath W B, Tushuizen Maarten E, Scheffer Peter G, Schalkwijk Casper G, Kamper Ad M, Stehouwer Coen D A
Institute for Cardiovascular Research, VU University Medical Centre, Amsterdam, Netherlands.
Atherosclerosis. 2003 Sep;170(1):59-72. doi: 10.1016/s0021-9150(03)00231-4.
This randomised double-blind, placebo-controlled, clinical trial investigated the effect of 3 months of treatment with calcium dobesilate on endothelium-dependent vasodilation, markers of endothelial function, blood pressure, and markers of oxidation in obese, male smokers. Vascular effects may depend on the type of vessel and we, therefore, investigated both smaller arteries, i.e. resistance arteries and small arterioles, and large conduit arteries. Vascular function was measured by acetylcholine- and sodium-nitroprusside-mediated vasodilation, and capillary recruitment, in the skin microcirculation; by forearm blood flow (FBF) responses to several agonists and to N-G-monomethyl L-arginine (L-NMMA) in the forearm vascular bed; by flow-mediated vasodilation in the brachial artery; and by determination of soluble levels of vascular cell adhesion molecule-1 (sVCAM-1), intercellular adhesion molecule-1 (sICAM-1) and E-selectin. Twenty-eight individuals received dobesilate and 24 placebo. No effect of calcium dobesilate on endothelial function, blood pressure or markers of oxidation was observed compared with placebo. The difference in acetylcholine-mediated vasodilation in the microcirculation was -52.1%-point (95% confidence interval -132.8 to 28.1); in sodium-nitroprusside-mediated vasodilation in the microcirculation, 2.6%-point (-95.1 to 100.2); in capillary recruitment, 2.5%-point (-6.8 to 11.7); in acetylcholine-induced increases in FBF (n=28), 23%-point (-173 to 126); in L-NMMA-induced reduction of basal FBF, -2.8%-point (-29.3 to 23.8); in flow-mediated vasodilation of the brachial artery, 0.3%-points (-2.7 to 3.3); in 24-h systolic blood pressure, 2.1 mmHg (-1.3 to 5.5); in soluble VCAM-1, 54 ng/ml (-8 to 115); in soluble ICAM-1, 9 ng/ml (-49 to 67); in sE-selectin, -17 ng/ml (-44 to 11); in ketocholesterol 5 nM (-17 to 26); and in oxidised LDL -1.6 U/l (-6.7 to 3.5). We have shown that endothelial function, blood pressure, and markers of oxidation were not affected by 3 months of treatment with calcium dobesilate in mildly obese, smoking men. Thus, our data provide no evidence of an effect on vascular function of calcium dobesilate in humans.
这项随机双盲、安慰剂对照的临床试验研究了3个月的羟苯磺酸钙治疗对肥胖男性吸烟者内皮依赖性血管舒张、内皮功能标志物、血压和氧化标志物的影响。血管效应可能取决于血管类型,因此,我们研究了较小的动脉,即阻力动脉和小动脉,以及大的输送动脉。通过乙酰胆碱和硝普钠介导的血管舒张以及皮肤微循环中的毛细血管募集来测量血管功能;通过前臂血管床中对几种激动剂和N-G-单甲基-L-精氨酸(L-NMMA)的前臂血流量(FBF)反应来测量;通过肱动脉中的血流介导的血管舒张来测量;以及通过测定血管细胞粘附分子-1(sVCAM-1)、细胞间粘附分子-1(sICAM-1)和E-选择素的可溶性水平来测量。28名个体接受了羟苯磺酸钙治疗,24名接受了安慰剂治疗。与安慰剂相比,未观察到羟苯磺酸钙对内皮功能、血压或氧化标志物有影响。微循环中乙酰胆碱介导的血管舒张差异为-52.1%(95%置信区间-132.8至28.1);微循环中硝普钠介导的血管舒张差异为2.6%(-95.1至100.2);毛细血管募集差异为2.5%(-6.8至11.7);乙酰胆碱诱导FBF增加(n = 28)差异为23%(-173至126);L-NMMA诱导基础FBF降低差异为-2.8%(-29.3至23.8);肱动脉血流介导的血管舒张差异为0.3%(-2.7至3.3);24小时收缩压差异为2.1 mmHg(-1.3至5.5);可溶性VCAM-1差异为54 ng/ml(-8至115);可溶性ICAM-1差异为9 ng/ml(-49至67);sE-选择素差异为-17 ng/ml(-44至11);酮胆固醇差异为5 nM(-17至26);氧化型低密度脂蛋白差异为-1.6 U/l(-6.7至3.5)。我们已经表明,在轻度肥胖的吸烟男性中,3个月的羟苯磺酸钙治疗不会影响内皮功能、血压和氧化标志物。因此,我们的数据没有提供羟苯磺酸钙对人体血管功能有影响的证据。