Weinberger M H
Hypertension Research Center, Indiana University School of Medicine, Indianapolis 46202-5111.
Eur Heart J. 1990 Jun;11(6):560-5. doi: 10.1093/oxfordjournals.eurheartj.a059750.
When combining a beta blocker with a diuretic in patients with hypertension, consideration should be given to the potential advantages of intrinsic sympathomimetic activity (ISA). During long-term administration of a beta blocker without ISA, total peripheral resistance stabilizes at or slightly above the pretreatment level. Since cardiac output is decreased, blood pressure falls. Thus, beta blockers without ISA may exacerbate the underlying haemodynamic abnormality of long-standing hypertension, increased systemic resistance. In contrast, the reduction in pressure which occurs with a beta blocker possessing a high degree of ISA, such as pindolol, is associated with a reduction in total peripheral resistance and little change in cardiac output. Thiazide diuretics and most beta blockers without ISA also have an adverse impact on the blood lipid profile, potentially increasing cardiovascular risk. With the exception of oxprenolol, monotherapy with beta blockers which possess ISA have generally had no adverse blood lipid changes. Indeed, pindolol has been shown to increase HDL-cholesterol and to reduce the ratio of total cholesterol to HDL-cholesterol. Pindolol administered in combination with several diuretics has not increased the adverse lipid effects of these agents and, in some studies, evidence suggests that pindolol may counteract some or all of these changes. The clinical significance of these differences between beta blockers with and without ISA remains uncertain. Nevertheless, the potential haemodynamic and metabolic benefit of agents with ISA mandate that they receive careful consideration when selecting a beta blocker to administer with a diuretic.
在高血压患者中联合使用β受体阻滞剂和利尿剂时,应考虑内在拟交感活性(ISA)的潜在优势。在长期使用无ISA的β受体阻滞剂期间,总外周阻力稳定在预处理水平或略高于预处理水平。由于心输出量降低,血压下降。因此,无ISA的β受体阻滞剂可能会加剧长期高血压潜在的血流动力学异常,即全身阻力增加。相比之下,具有高度ISA的β受体阻滞剂(如吲哚洛尔)引起的血压降低与总外周阻力降低和心输出量变化不大有关。噻嗪类利尿剂和大多数无ISA的β受体阻滞剂也会对血脂谱产生不利影响,可能增加心血管风险。除氧烯洛尔外,单药使用具有ISA的β受体阻滞剂一般不会引起不良血脂变化。事实上,吲哚洛尔已被证明可增加高密度脂蛋白胆固醇,并降低总胆固醇与高密度脂蛋白胆固醇的比率。吲哚洛尔与几种利尿剂联合使用并未增加这些药物的不良血脂影响,并且在一些研究中,有证据表明吲哚洛尔可能抵消部分或全部这些变化。有ISA和无ISA的β受体阻滞剂之间这些差异的临床意义仍不确定。然而,具有ISA的药物潜在的血流动力学和代谢益处要求在选择与利尿剂联合使用的β受体阻滞剂时仔细考虑它们。