Tawakol Ahmed, Forgione Marc A, Stuehlinger Markus, Alpert Nathaniel M, Cooke John P, Loscalzo Joseph, Fischman Alan J, Creager Mark A, Gewirtz Henry
Departments of Medicine (Cardiac Unit), Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
J Am Coll Cardiol. 2002 Sep 18;40(6):1051-58. doi: 10.1016/s0735-1097(02)02069-7.
We sought to use positron emission tomography (PET) to test the hypothesis that hyperhomocysteinemia adversely effects coronary microvascular dilator function.
Hyperhomocysteinemia is associated with abnormal endothelium-dependent vasodilation in peripheral human arteries. However, its effect on the coronary circulation is not known.
Eighteen healthy humans, age 24 to 56 years, were enrolled in a double-blind, crossover trial. Basal and adenosine-stimulated myocardial blood flow (MBF) was determined by PET: after ingestion of placebo and after methionine-induced hyperhomocysteinemia. Further, brachial ultrasonography was used to assess flow-mediated vasodilation. Additionally, to assess the role of nitric oxide (NO) in adenosine-mediated vasodilation, the MBF response to adenosine was measured in the presence and absence of the NO synthase antagonist NG-monomethyl-l-arginine (l-NMMA) (0.3 mg/kg/min intravenously).
Hyperhomocysteinemia resulted in a reduction in the MBF dose-response curve to adenosine (p < 0.05). This was most apparent with low dose adenosine, where MBF augmentation was significantly blunted during hyperhomocysteinemia (1.06 +/- 1.00 ml/min/g vs. 0.58 +/- 0.78 ml/min/g, placebo vs. methionine, p < 0.05). Similarly, flow-mediated brachial artery vasodilation was impaired during hyperhomocysteinemia (4.4 +/- 2.6% vs. 2.6 +/- 2.3%, placebo vs. methionine, p < 0.05). In a separate series of experiments, MBF during adenosine was reduced in the presence of l-NMMA (p < 0.05 analysis of variance). This was most apparent at the low dose of adenosine, where MBF response to adenosine was blunted in the presence of l-NMMA (2.08 +/- 1.34 ml/min/g vs. 1.48 +/- 1.32 ml/min/g, placebo vs. l-NMMA, p < 0.05).
The data, therefore, support the hypothesis that acute hyperhomocysteinemia impairs microvascular dilation in the human coronary circulation as a result of reduced NO bioavailability.
我们试图利用正电子发射断层扫描(PET)来验证高同型半胱氨酸血症对冠状动脉微血管扩张功能产生不利影响这一假说。
高同型半胱氨酸血症与人体外周动脉中内皮依赖性血管舒张异常有关。然而,其对冠状动脉循环的影响尚不清楚。
18名年龄在24至56岁之间的健康人参与了一项双盲交叉试验。通过PET测定基础状态下以及腺苷刺激后的心肌血流量(MBF):分别在摄入安慰剂后以及蛋氨酸诱导的高同型半胱氨酸血症后进行测定。此外,使用肱动脉超声检查来评估血流介导的血管舒张。另外,为了评估一氧化氮(NO)在腺苷介导的血管舒张中的作用,在存在和不存在NO合酶拮抗剂N-甲基-L-精氨酸(L-NMMA)(0.3mg/kg/分钟静脉注射)的情况下测量对腺苷的MBF反应。
高同型半胱氨酸血症导致对腺苷的MBF剂量反应曲线降低(p<0.05)。这在低剂量腺苷时最为明显,在高同型半胱氨酸血症期间MBF增加明显减弱(安慰剂组与蛋氨酸组相比,1.06±1.00ml/分钟/克 vs. 0.58±0.78ml/分钟/克,p<0.05)。同样,在高同型半胱氨酸血症期间血流介导的肱动脉血管舒张受损(安慰剂组与蛋氨酸组相比,4.4±2.6% vs. 2.6±2.3%,p<0.05)。在另一系列实验中,在存在L-NMMA的情况下腺苷期间的MBF降低(方差分析,p<0.05)。这在低剂量腺苷时最为明显,在存在L-NMMA的情况下对腺苷的MBF反应减弱(安慰剂组与L-NMMA组相比,2.08±1.34ml/分钟/克 vs. 1.48±1.32ml/分钟/克,p<0.05)。
因此,数据支持这样的假说,即急性高同型半胱氨酸血症由于NO生物利用度降低而损害人体冠状动脉循环中的微血管扩张。