Bondjers G
Wallenberg Laboratory for Cardiovascular Research, University of Göteborg, Sweden.
Eur Heart J. 1994 Aug;15 Suppl C:8-15. doi: 10.1093/eurheartj/15.suppl_c.8.
Mechanisms involved in the development of atherosclerosis are reviewed. Based primarily on experimental studies, the following key steps are suggested; (1) endothelial injury; (2) platelet and leukocyte adhesion; (3) smooth muscle proliferation; (4) lipid deposition; (5) arterial tissue hypoxia. Beta-blockers may interfere with (1), (2), (4) and (5), and have been shown to inhibit experimental atherosclerosis, even if given after the disease has been established. Calcium channel and ACE inhibitors interfere with (2), and have been shown to inhibit experimental atherosclerosis if given throughout the experimental period. It is unclear whether the association between hypertension and atherosclerosis is causal. Therefore, antihypertensive agents should be selected according to their potential to interfere with the atherosclerotic process. The primary choice would then be beta-blockers, combined with calcium channel or ACE inhibitors if the patient is considered to be at risk of developing new lesions.
本文综述了动脉粥样硬化发生发展过程中涉及的机制。主要基于实验研究,提出了以下关键步骤:(1)内皮损伤;(2)血小板和白细胞黏附;(3)平滑肌增殖;(4)脂质沉积;(5)动脉组织缺氧。β受体阻滞剂可能会干扰(1)、(2)、(4)和(5),并且已被证明可抑制实验性动脉粥样硬化,即使在疾病已形成后给予也有效。钙通道阻滞剂和血管紧张素转换酶(ACE)抑制剂会干扰(2),并且已被证明在整个实验期间给予时可抑制实验性动脉粥样硬化。高血压与动脉粥样硬化之间的关联是否具有因果关系尚不清楚。因此,应根据抗高血压药物干扰动脉粥样硬化进程的潜力来选择药物。首选药物应为β受体阻滞剂,如果患者被认为有发生新病变的风险,则可联合使用钙通道阻滞剂或ACE抑制剂。