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新出现的概念:冠状动脉疾病中的血管紧张素转换酶抑制作用

Emerging concepts: angiotensin-converting enzyme inhibition in coronary artery disease.

作者信息

Mancini G B

机构信息

Department of Medicine, University of British Columbia, Vancouver, Canada.

出版信息

Cardiovasc Drugs Ther. 1996 Nov;10 Suppl 2:609-12. doi: 10.1007/BF00052506.

Abstract

Angiotensin-converting enzyme (ACE) inhibitors have played a highly beneficial role in the therapy of hypertension and congestive heart failure. Detailed analysis of some of the heart failure trials in patients with these diseases has uncovered unexpected benefits in the prevention of cardiovascular events. Paralleling these observations are the rapidly accruing basic studies describing important molecular and cellular effects of these agents. For example, ACE inhibition will prevent stimulation of smooth muscle cell angiotensin II receptors, thereby blocking both contractile and proliferative actions. In addition, ACE inhibition of kininase II inhibits the breakdown of bradykinin. Bradykinin is a direct stimulant of nitric oxide release from the intact endothelial cell. Thus, at the cellular level ACE inhibition shifts the balance of ongoing mechanisms in favor of those promoting vasodilatory, antiaggregatory, antithrombotic, and antiproliferative effects. These effects underlie the potential benefits of ACE inhibition in the therapy of coronary artery disease and atherosclerosis.

摘要

血管紧张素转换酶(ACE)抑制剂在高血压和充血性心力衰竭的治疗中发挥了非常有益的作用。对患有这些疾病的患者进行的一些心力衰竭试验的详细分析发现,在预防心血管事件方面有意外的益处。与这些观察结果平行的是,迅速积累的基础研究描述了这些药物重要的分子和细胞效应。例如,ACE抑制可防止平滑肌细胞血管紧张素II受体的刺激,从而阻断收缩和增殖作用。此外,ACE对激肽酶II的抑制作用可抑制缓激肽的分解。缓激肽是完整内皮细胞释放一氧化氮的直接刺激物。因此,在细胞水平上,ACE抑制使现有机制的平衡向有利于促进血管舒张、抗聚集、抗血栓形成和抗增殖作用的方向转变。这些效应是ACE抑制在冠状动脉疾病和动脉粥样硬化治疗中潜在益处的基础。

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