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首页> 外文期刊>Journal of hypertension >Advanced glycation endproduct crosslink breaker (alagebrium) improves endothelial function in patients with isolated systolic hypertension.
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Advanced glycation endproduct crosslink breaker (alagebrium) improves endothelial function in patients with isolated systolic hypertension.

机译:晚期糖基化终产物交联破坏剂(alagebrium)可改善单纯性收缩期高血压患者的内皮功能。

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OBJECTIVES: Arterial stiffening and endothelial dysfunction are hallmarks of aging, and advanced glycation endproducts (AGE) may contribute to these changes. We tested the hypothesis that AGE crosslink breakers enhance endothelial flow-mediated dilation (FMD) in humans and examined the potential mechanisms for this effect. METHODS: Thirteen adults (nine men, aged 65 +/- 2 years) with isolated systolic hypertension (systolic blood pressure > 140 mmHg, diastolic blood pressure < 90 mmHg or pulse pressure > 60 mmHg) on stable antihypertensive therapy were studied. Subjects received placebo (2 weeks) then oral alagebrium (ALT-711; 210 mg twice a day for 8 weeks). Subjects and data analyses were blinded to treatment. Arterial stiffness was assessed by carotid augmentation index (AI) and brachial artery distensibility (ArtD) using applanation tonometry and Doppler echo, and endothelial function by brachial FMD. Serum markers of collagen metabolism and vascular inflammation were assessed. RESULTS: Alagebrium reduced carotid AI by 37% (P = 0.007) and augmented pressure (16.4 +/- 10 to 9.6 +/- 9 mmHg; P < 0.001). Heart rate, arterial pressures, and ArtD, were unchanged. FMD increased from 4.6 +/- 1.1 to 7.1 +/- 1.1% with alagebrium (P < 0.05), and was unrelated to altered shear stress or regional arterial distensibility. However, FMD change was inversely related to markers of collagen synthesis, p-selectin and intracellular cell adhesion molecule (all P < 0.05). Alagebrium-associated changes in plasma nitrite plus nitrate was inversely correlated with plasma matrix metalloproteinase 9 and type I collagen (P = 0.007). CONCLUSIONS: Alagebrium enhances peripheral artery endothelial function and improves overall impedance matching. Improved endothelial function correlates better with reduced vascular fibrosis and inflammation markers than with vessel distensibility. AGE-crosslink breakers may reduce cardiovascular risk in older adults by reduced central arterial stiffness and vascular remodeling.
机译:目的:动脉硬化和内皮功能障碍是衰老的标志,晚期糖基化终产物(AGE)可能有助于这些变化。我们测试了AGE交联剂在人中增强内皮流介导的扩张(FMD)的假说,并研究了这种作用的潜在机制。方法:研究了13名成年人,他们接受了稳定的降压治疗,他们均患有单纯收缩期高血压(收缩压> 140 mmHg,舒张压<90 mmHg或脉压> 60 mmHg)。受试者接受安慰剂(2周),然后口服alagebrium(ALT-711;每天两次,共210 mg,共8周)。受试者和数据分析对治疗不知情。使用压平术和多普勒回声通过颈动脉扩张指数(AI)和肱动脉扩张性(ArtD)评估动脉僵硬度,并通过肱FMD评估内皮功能。评估了胶原代谢和血管炎症的血清标志物。结果:Alagebrium使颈动脉AI降低了37%(P = 0.007),压力增加了(16.4 +/- 10至9.6 +/- 9 mmHg; P <0.001)。心率,动脉压和ArtD均未改变。带有alagebrium的FMD从4.6 +/- 1.1增加到7.1 +/- 1.1%(P <0.05),并且与剪切应力的改变或区域动脉扩张性无关。但是,FMD的变化与胶原蛋白合成标记,p-选择素和细胞内细胞粘附分子呈负相关(所有P <0.05)。血浆亚硝酸盐和硝酸盐与Alagebrium相关的变化与血浆基质金属蛋白酶9和I型胶原呈负相关(P = 0.007)。结论:Alagebrium可增强外周动脉内皮功能并改善总体阻抗匹配。改善的内皮功能与减少血管纤维化和炎症标志物的相关性比与血管扩张性的相关性更好。 AGE交联剂可以通过降低中央动脉僵硬度和血管重塑来降低老年人的心血管风险。

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