Engel B, Einstein R, Goodman A H
Eur J Pharmacol. 1983 Jan 21;86(3-4):461-6. doi: 10.1016/0014-2999(83)90197-8.
The use of different methods of measuring contractility and the effects of cardiovascular reflexes are among the factors which complicate the assessment of selective inotropic activity of beta-adrenoceptor agonists. The effects of dobutamine, prenalterol, noradrenaline and isoprenaline on heart rate, iliac blood flow, left ventricular pressure, max dP/dt and (dP/dt) divided by IIT (integrated isometric tension) were evaluated in anaesthetised dogs in which the hearts were denervated and blood pressure held constant. All the drugs caused dose-dependent increases in heart rate and contractility. The relative chronotropic and inotropic activity of each agonist was evaluated. At most doses studied the agonists exerted similar chronotropic and inotropic activity when compared to the non-selective agonist isoprenaline. It is likely that the inotropic selectivity observed with prenalterol and dobutamine in previous studies depends on factors other than direct drug action.
使用不同的收缩性测量方法以及心血管反射的影响是使β-肾上腺素能受体激动剂的选择性正性肌力活性评估复杂化的因素之一。在麻醉的、心脏去神经支配且血压保持恒定的犬中,评估了多巴酚丁胺、普瑞特罗、去甲肾上腺素和异丙肾上腺素对心率、髂血流量、左心室压力、最大dP/dt以及(dP/dt)除以IIT(等长收缩张力积分)的影响。所有药物均引起心率和收缩性的剂量依赖性增加。评估了每种激动剂的相对变时性和正性肌力活性。在大多数研究剂量下,与非选择性激动剂异丙肾上腺素相比,这些激动剂表现出相似的变时性和正性肌力活性。先前研究中观察到的普瑞特罗和多巴酚丁胺的正性肌力选择性可能取决于直接药物作用以外的因素。