Hjalmarson A
Institute of Heart and Lung Diseases, Sahlgrenska University Hospital, Göteborg, Sweden.
Basic Res Cardiol. 2000;95 Suppl 1:I41-5. doi: 10.1007/s003950070008.
Beta-blockers have several beneficial cardiovascular effects in patients with hypertension, angina pectoris, myocardial infarction, and congestive heart failure. In patients with myocardial infarction and congestive heart failure some beta-blockers have been found to reduce mortality and morbidity. The beta-blockers with a proven effect on prognosis include timolol, metoprolol, propranolol, bisoprolol, and carvedilol. One important question is whether all cardiovascular effects obtained by beta-blockers can be considered to be class effects. The beta-blockers with favorable effects on prognosis include two with more selective beta1-receptor blockade (metoprolol and bisoprolol) and three non-selective (timolol, propranolol and carvedilol). One non-selective beta-blocker, which also has a more pronounced class III effect, sotalol, has been studied in a large postinfarction study without a significant effect on mortality. However, sotalol reduced the incidence of reinfarction similarly to the other beta-blockers with proven effect on mortality after myocardial infarction. Sotalol had no influence at all on sudden cardiac death, while all the other beta-blockers referred to above have a very marked effect on sudden cardiac death, in fact more marked than on overall mortality. The beta-blockers with proven effect on mortality and on sudden death have one property in common and that is some degreee of lipophilicity. Sotalol and atenolol are hydrophilic. From animal experimental data it has been suggested that beta-bockers with some degree of lipophilicity penetrate into the brain and have an indirect effect on vagal activity, which is of importance for prevention of ventricular fibrillation and sudden cardiac death. It can be summarized that some beta-blockers have been found to reduce mortality and sudden cardiac death in patients after myocardial infarction and in congestive heart failure, while others have not. It seems that the major properties of the beta-blockers with proven effects on mortality and sudden cardiac death are beta1-receptor blockade and some degree of lipophilicity. Until we know more about the mechanisms behind prevention of death and especially sudden cardiac death by beta-blockers, only drugs with proven effects on prognosis should be used.
β受体阻滞剂对高血压、心绞痛、心肌梗死和充血性心力衰竭患者具有多种有益的心血管效应。在心肌梗死和充血性心力衰竭患者中,已发现某些β受体阻滞剂可降低死亡率和发病率。已证实对预后有影响的β受体阻滞剂包括噻吗洛尔、美托洛尔、普萘洛尔、比索洛尔和卡维地洛。一个重要的问题是,β受体阻滞剂所产生的所有心血管效应是否都可被视为类效应。对预后有有利影响的β受体阻滞剂包括两种具有更强选择性β1受体阻滞作用的药物(美托洛尔和比索洛尔)以及三种非选择性药物(噻吗洛尔、普萘洛尔和卡维地洛)。一种非选择性β受体阻滞剂索他洛尔,也具有更显著的Ⅲ类效应,在一项大型心肌梗死后研究中对死亡率无显著影响。然而,索他洛尔与其他已证实对心肌梗死后死亡率有影响的β受体阻滞剂一样,降低了再梗死的发生率。索他洛尔对心源性猝死完全没有影响,而上述所有其他β受体阻滞剂对心源性猝死有非常显著的影响,实际上比对总死亡率的影响更显著。已证实对死亡率和猝死有影响的β受体阻滞剂有一个共同特性,即具有一定程度的脂溶性。索他洛尔和阿替洛尔是亲水性的。从动物实验数据来看,已表明具有一定程度脂溶性的β受体阻滞剂可穿透进入大脑,并对迷走神经活动产生间接影响,这对于预防室颤和心源性猝死很重要。可以总结出,已发现某些β受体阻滞剂可降低心肌梗死患者和充血性心力衰竭患者的死亡率和心源性猝死,而其他一些则没有。似乎已证实对死亡率和心源性猝死有影响的β受体阻滞剂的主要特性是β1受体阻滞作用和一定程度的脂溶性。在我们更多地了解β受体阻滞剂预防死亡尤其是心源性猝死背后的机制之前,仅应使用已证实对预后有影响的药物。