参麦注射液对冠心病患者血管内皮依赖性舒张功能的影响

中国中西医结合杂志 Pub Date : 2017-03-01
Yan Zhou, Hang-Yuan Guo, Fang Pneg
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引用次数: 0

摘要

目的观察参麦注射液(SI)对冠心病(CHD)患者血管内皮依赖性舒张功能的影响。方法将100例冠心病患者随机分为SI组和对照组,每组各50例。所有患者均接受常规冠心病药物治疗,每组50例。SI组患者静脉注射SI,每次50 mL,每天1次,连用10天。在治疗前和治疗后第10天,用血管内超声测量所有患者在充血和舌下硝酸甘油时肱动脉内径的变化。采用生化法和ELISA法检测血清NO水平、血浆内皮素(ET)、血栓素B 2 (TXB 2)、6-酮- pgf 1 α、超氧化物歧化酶(SOD)水平。招募30例经冠状动脉CT或冠状动脉造影证实的非冠心病患者作为非冠心病组。结果冠心病组血充血及舌下硝酸甘油后肱动脉内径改变值较非冠心病组明显降低(P
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effect of Shenmai Injection on Vascular Endothelial Dependence Diastolic Function in Coronary Heart Disease Patients].

Objective To observe the effect of Shenmai Injection (SI) on vascular endothelial dependent diastolic function in coronary heart disease (CHD) patients. Methods Totally 100 recruited CHD patients were assigned to the SI group and the control group by random digit table, 50 in each group. All patients received conventional drugs for CHD, 50 in each group. Patients in the SI group were intrave- nously injected with SI, 50 mL each time, once per day for 10 days. Changes of brachial artery diameter at hyperemia and sublingual nitroglycerin were measured in all patients before treatment and at day 10 after treatment by intravascular ultrasound. Serum NO level, plasma levels of endothelin (ET) , thromboxane B₂ (TXB₂), 6-keto-PGF₁α , superoxide dismutase (SOD) were measured using biochemical assay and ELISA. Thirty non-CHD patients confirmed with coronary CT or coronary angiogram were recruited as the non-CHD group. Results Changed value of brachial artery diameter at hyperemia and after sublingual nitroglycerin were more obviously reduced in the CHD group than in the non-CHD group (P <0. 05, P <0. 01). Besides, levels of NO, 6-keto-PGF1α were lowered, levels of ET and TXB₂ were elevated (P < 0. 01). Compared with the control group, congestion of brachial artery was significantly improved, levels of NO and 6-keto-PGF₁α increased, SOD concentration was obviously elevated, plasma levels of ET and TXB₂ decreased in the SI group (all P <0. 05). Conclusion SI could directly up-regulate levels of NO and 6-keto-PGF₁α , increase SOD activity, decrease levels of ET and TXB₂ , and improve vascular endothelial dependent vasodilation.

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