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氨氯地平降压反应与小而密的 HDL3 的抗氧化活性之间的关系。

Blood pressure-lowering response to amlodipine as a determinant of the antioxidative activity of small, dense HDL3.

机构信息

Service d'Endocrinologie-Métabolisme, Hôpital de la Pitié, Paris, France.

出版信息

Am J Cardiovasc Drugs. 2011 Oct 1;11(5):317-25. doi: 10.2165/11592280-000000000-00000.

Abstract

BACKGROUND AND OBJECTIVE

High-density lipoproteins (HDLs) exert multiple antiatherogenic activities including protection of low-density lipoproteins (LDLs) from oxidative stress. Beneficial effects of calcium channel blockers on cardiovascular disease may in part be related to the reduction of oxidative stress, potentially enhancing the antioxidative activity (AOX) of HDLs. This study aimed to assess the effect of 1 month's treatment with amlodipine on HDL AOX in hypertensive subjects.

METHODS

This was a prospective trial of amlodipine 10 mg/day administered for 1 month in primary-care patients with hypertension (n = 28), 46% of whom were obese and 57% of whom displayed the metabolic syndrome. The main outcome measure was HDL AOX, assessed as the capacity of small, dense HDL3c particles to attenuate LDL oxidation induced in vitro by an azo initiator (AAPH).

RESULTS

Mean (± SD) systolic (SBP) and diastolic (DBP) BP were reduced by amlodipine by 22.1 mmHg (± 13.2) and 10.4 mmHg (± 7.5), respectively (p < 0.001). Body mass index, waist circumference, and plasma levels of triglycerides, cholesterol, and fasting blood glucose did not change significantly. Amlodipine treatment did not modify HDL3c AOX in the whole study population; changes in AOX were, however, positively correlated with SBP (r = 0.37, p = 0.05 for maximal diene concentration; r = 0.34, p = 0.08 for LDL oxidation rate). When the population was divided into two subgroups according to the BP response to amlodipine (change in SBP below or above the median), HDL3c AOX was significantly improved in hyper-responders (BP-lowering response >22/10 mmHg) as compared with hypo-responders (BP-lowering response <22/10 mmHg: mean [± SD] change in the LDL oxidation rate in the presence of HDL3c, -6.8% [± 11.2] vs +1.9% [± 5.2], respectively, p = 0.04; maximal diene concentration, -8.6% [± 13.0] vs +1.9% [± 8.2], respectively, p < 0.05). By contrast, neither plasma concentrations of oxidized LDL, a marker of systemic oxidative stress, nor the chemical composition of HDL3c were modified between the subgroups.

CONCLUSIONS

In hypertensive patients, amlodipine treatment enhanced HDL AOX in subjects who had a BP reduction that exceeded the median response. This effect appears to be secondary to the hypotensive effect, rather than to the direct antioxidant properties, of the drug.

摘要

背景与目的

高密度脂蛋白(HDL)具有多种抗动脉粥样硬化作用,包括保护低密度脂蛋白(LDL)免受氧化应激。钙通道阻滞剂对心血管疾病的有益作用可能部分与氧化应激的减少有关,这可能增强了 HDL 的抗氧化活性(AOX)。本研究旨在评估氨氯地平治疗 1 个月对高血压患者 HDL AOX 的影响。

方法

这是一项前瞻性研究,在初级保健患者中使用氨氯地平 10mg/天治疗 1 个月,这些患者患有高血压(n=28),其中 46%肥胖,57%患有代谢综合征。主要观察指标是 HDL AOX,评估小而密的 HDL3c 颗粒减弱体外由偶氮引发剂(AAPH)诱导的 LDL 氧化的能力。

结果

氨氯地平治疗使收缩压(SBP)和舒张压(DBP)平均(±SD)分别降低 22.1mmHg(±13.2)和 10.4mmHg(±7.5)(p<0.001)。体重指数、腰围和血浆甘油三酯、胆固醇和空腹血糖水平无明显变化。氨氯地平治疗并未改变整个研究人群中 HDL3c AOX;然而,AOX 的变化与 SBP 呈正相关(最大二烯浓度的 r=0.37,p=0.05;LDL 氧化速率的 r=0.34,p=0.08)。当根据氨氯地平对血压的反应(SBP 降低大于或小于中位数)将人群分为两个亚组时,与低反应者(降压反应<22/10mmHg)相比,高反应者(降压反应>22/10mmHg)的 HDL3c AOX 显著改善(LDL 氧化速率存在时的 HDL3c 的平均[±SD]变化,-6.8%[±11.2]与+1.9%[±5.2],分别,p=0.04;最大二烯浓度,-8.6%[±13.0]与+1.9%[±8.2],分别,p<0.05)。相比之下,两组之间血浆氧化 LDL 浓度(全身氧化应激的标志物)或 HDL3c 的化学组成均未发生变化。

结论

在高血压患者中,氨氯地平治疗增强了血压降低超过中位数反应的患者的 HDL AOX。这种作用似乎是药物降压作用的结果,而不是其直接抗氧化特性的结果。

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