首页> 美国卫生研究院文献>British Journal of Clinical Pharmacology >Haemodynamic effects of atenolol labetalol pindolol and captopril: a comparison in hypertensive patients with special reference to changes in limb blood flow heart rate and left ventricular function.
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Haemodynamic effects of atenolol labetalol pindolol and captopril: a comparison in hypertensive patients with special reference to changes in limb blood flow heart rate and left ventricular function.

机译:阿替洛尔拉贝洛尔哌多洛尔和卡托普利的血流动力学效应:高血压患者的比较特别涉及肢体血流量心率和左心室功能的变化。

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摘要

1 To compare the haemodynamic effects of secondary characteristics of beta-adrenoceptor blockers with an angiotensin converting enzyme inhibitor forty patients with previously untreated mild to moderate hypertension were prescribed either atenolol 50-100 mg day-1, labetalol 200-800 mg day-1, pindolol 10-30 mg day-1 or captopril 25-100 mg day-1 and observed for 6 months. 2 Over this period: (a) All four drugs produced similar reductions in blood pressure at rest (P less than or equal to 0.01) and after exercise (P less than or equal to 0.01). (b) All four drugs significantly decreased resting forearm (P less than or equal to 0.01) and calf blood flow (P less than or equal to 0.01). They all also caused a significant reduction in the increased calf blood flow following exercise (P less than or equal to 0.01). (c) No drug produced a change in resting forearm vascular resistance, while resting calf vascular resistance was decreased by captopril and pindolol, unaltered by labetalol and increased by atenolol. Post-exercise calf vascular resistance was increased by atenolol, labetalol and pindolol but unaltered by captopril. (d) Although all four drugs produced a fall in resting heart rate this was significantly greater for atenolol and labetalol (P less than or equal to 0.01). All four treatments however significantly reduced the increase in heart rate following exercise (P less than or equal to 0.01). (e) No drug produced any significant change in resting and post-exercise stroke volume/ejection fraction. 3 It is concluded that despite differing modes of action all four drugs reduce limb blood flow. This primarily appears to be a consequence of reduced perfusion pressure associated with limited autoregulation of skeletal muscle circulation. The reduction in arterial vascular resistance produced by captopril and pindolol is inconsistent and does not appear of major benefit in preserving limb blood flow. The reduction in perfusion with the agents studied may in part be related to a fall in cardiac output associated with decreased heart rate. This suggests that captopril may exert antisympathetic activity when used as an antihypertensive agent.
机译:1为了比较β-肾上腺素受体阻滞剂与血管紧张素转化酶抑制剂的继发特性对血液动力学的影响,对40名先前未接受过轻度至中度高血压治疗的患者开具了阿替洛尔50-100 mg第1天,拉贝洛尔200-800 mg第1天的处方,服用第1天的10-30 mg品多洛尔或服用第1天的25-100 mg卡托普利,并观察6个月。 2在此期间:(a)四种药物在休息时(P小于或等于0.01)和运动后(P小于或等于0.01)的血压均出现相似的降低。 (b)所有四种药物均显着降低了前臂的静息时间(P小于或等于0.01)和小腿血流量(P小于或等于0.01)。它们也都导致运动后小腿血流量增加的显着减少(P小于或等于0.01)。 (c)没有药物产生静息前臂血管阻力的变化,而卡托普利和匹多洛尔降低了静息小腿的血管阻力,拉贝洛尔不变,而阿替洛尔则增加了。运动后小牛的血管阻力被阿替洛尔,拉贝洛尔和哌多洛尔增加,但卡托普利未改变。 (d)尽管所有四种药物均使静息心率下降,但阿替洛尔和拉贝洛尔的心率却明显更高(P小于或等于0.01)。然而,所有四种治疗均显着降低了运动后心率的增加(P小于或等于0.01)。 (e)没有药物在静息和运动后中风量/射血分数方面产生任何显着变化。 3结论是,尽管有不同的作用方式,所有四种药物均会降低肢体血流量。这主要是由于与骨骼肌循环的有限自动调节相关的灌注压力降低的结果。卡托普利和匹多洛尔引起的动脉血管阻力的降低是不一致的,并且在保持肢体血流方面没有明显的益处。所研究药物的灌注减少可能部分与心率降低相关的心输出量下降有关。这表明卡托普利用作抗高血压药时可能发挥抗交感作用。

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