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血管紧张素转换酶抑制剂和钙拮抗剂的血管保护作用:高血压及其他心血管疾病联合治疗的理论基础

Vascular protective effects of ACE inhibitors and calcium antagonists: theoretical basis for a combination therapy in hypertension and other cardiovascular diseases.

作者信息

Lüscher T F, Wenzel R R, Moreau P, Takase H

机构信息

Cardiology & Cardiovascular Research, University Hospital, Bern, Switzerland.

出版信息

Cardiovasc Drugs Ther. 1995 Aug;9 Suppl 3:509-23. doi: 10.1007/BF00877863.

Abstract

Hypertension is an important cardiovascular risk factor. High blood pressure per se is not a disease but a hemodynamic alteration associated with vascular disease. Two classes of drugs are especially effective in lowering blood pressure and preventing cardiovascular complications, angiotensin converting enzyme (ACE) inhibitors and calcium antagonists. The hemodynamic effects of ACE inhibitors and calcium antagonists are complementary. While ACE inhibitors inhibit the renin-angiotensin system and reduce sympathetic outflow, calcium antagonists dilate large conduit and resistance arteries. Certain calcium antagonists, such as verapamil, lower heart rate. In the blood vessel wall, the local vascular effects of ACE inhibitors and calcium antagonists are also complementary. While ACE inhibitors inhibit activation of angiotensin I into angiotensin II and prevent the breakdown of bradykinin (which stimulates nitric oxide and prostacyclin formation), calcium antagonists inhibit the effects of vasoconstrictor hormones such as angiotensin II at the level of vascular smooth muscle by reducing calcium inflow and facilitating the vasodilator effects of nitric oxide. Calcium antagonists reduce smooth muscle cell proliferation and atherosclerosis. In hypertensive animals, verapamil and trandolapril normalize endothelial dysfunction. In large angiographic trials, nifedipine and nicardipine reduced the development of new atherosclerotic plaques. After myocardial infarction, verapamil reduces mortality and cardiac events in patients without heart failure. In contrast, ACE inhibitors are effective after myocardial infarction in patients with impaired left ventricular function. Urinary albumin excretion rate decreases during ACE inhibitor therapy or with a calcium antagonist such as verapamil; combination of the two drugs has an additive effect. In resistance arteries, hypertension is associated with an increased media/lumen ratio. ACE inhibitors, but not beta-blockers, markedly improve these structural changes. In summary, ACE inhibitors and calcium antagonists have a complementary profile, both in their hemodynamic and local vascular action. Hence, combination therapy with these two classes of drugs appears particularly useful in patients with hypertension, not only to lower blood pressure, but hopefully to achieve improved cardiovascular protection.

摘要

高血压是一种重要的心血管危险因素。高血压本身并非一种疾病,而是与血管疾病相关的血流动力学改变。两类药物在降低血压和预防心血管并发症方面特别有效,即血管紧张素转换酶(ACE)抑制剂和钙拮抗剂。ACE抑制剂和钙拮抗剂的血流动力学效应是互补的。ACE抑制剂抑制肾素-血管紧张素系统并减少交感神经输出,而钙拮抗剂则扩张大的输送血管和阻力动脉。某些钙拮抗剂,如维拉帕米,可降低心率。在血管壁中,ACE抑制剂和钙拮抗剂的局部血管效应也是互补的。ACE抑制剂抑制血管紧张素I转化为血管紧张素II,并阻止缓激肽(刺激一氧化氮和前列环素形成)的分解,而钙拮抗剂通过减少钙内流并促进一氧化氮的血管舒张作用,在血管平滑肌水平抑制血管收缩激素如血管紧张素II的作用。钙拮抗剂可减少平滑肌细胞增殖和动脉粥样硬化。在高血压动物中,维拉帕米和群多普利可使内皮功能障碍恢复正常。在大型血管造影试验中,硝苯地平和尼卡地平减少了新动脉粥样硬化斑块的形成。心肌梗死后,维拉帕米可降低无心力衰竭患者的死亡率和心脏事件。相比之下,ACE抑制剂对左心室功能受损的心肌梗死患者有效。在ACE抑制剂治疗期间或使用钙拮抗剂如维拉帕米时,尿白蛋白排泄率会降低;两种药物联合使用具有相加作用。在阻力动脉中,高血压与中膜/管腔比值增加有关。ACE抑制剂而非β受体阻滞剂可显著改善这些结构变化。总之,ACE抑制剂和钙拮抗剂在血流动力学和局部血管作用方面具有互补性。因此,这两类药物联合治疗对高血压患者似乎特别有用,不仅可降低血压,而且有望实现更好的心血管保护。

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